The present invention relates to a memory device and a semiconductor device including the memory device.
In recent years, a metal oxide having semiconductor characteristics, which is called an oxide semiconductor, has attracted attention as a novel semiconductor material having high mobility as in the case of polysilicon or microcrystalline silicon and having uniform element characteristics as in the case of amorphous silicon. The metal oxide is used for various applications; for example, indium oxide is a well-known metal oxide and used as a material of a pixel electrode in a liquid crystal display device. Examples of such metal oxides having semiconductor characteristics include tungsten oxide, tin oxide, indium oxide, and zinc oxide. Transistors in each of which a channel formation region is formed using such a metal oxide having semiconductor characteristics have been known (Patent Documents 1 and 2).
Examples of a semiconductor memory device (hereinafter, simply referred to as a memory device) include a DRAM and an SRAM which are categorized as a volatile memory; a mask ROM, an EPROM, an EEPROM, a flash memory, and a ferroelectric memory which are categorized as a nonvolatile memory; and the like. Most of these memories including single crystal semiconductor substrates are already put into practical use. Among the above memory devices, a DRAM has a simple structure in which a memory cell includes a transistor and a capacitor and needs fewer semiconductor elements for forming a memory cell than other memory devices such as an SRAM. Therefore, memory capacity per unit area can be increased as compared to other memory devices, and thus, a DRAM is advantageous in cost reduction.
As described above, a DRAM is suitable for large storage capacity, but memory capacity per unit area needs to be further increased as in other memory devices in order that an integrated circuit having higher degree of integration is realized while an increase in a chip size is suppressed. For that purpose, the area of a capacitor for holding charge provided in each memory cell has to be reduced and the area of each memory cell has to be reduced.
However, as the capacitance value is decreased due to reduction in the area of a capacitor, difference between the amounts of charge of digital values (e.g., difference between the amount of charge corresponding to “1” and the amount of charge corresponding to “0”) becomes smaller. Thus, if a slight amount of off-state current exists in the transistor, it is difficult to maintain the accuracy of data, and a holding period tends to be short. Accordingly, frequency of refresh operation is increased and power consumption is increased.
In view of the above problem, an object of the present invention is to propose a memory device in which a period in which data is held is ensured and memory capacity per unit area can be increased. Further, an object of the present invention is to propose a semiconductor device including the memory device.
In the disclosed invention, a memory device is formed using a material capable of sufficiently reducing the off-state current of a transistor, such as an oxide semiconductor material that is a wide gap semiconductor. The oxide semiconductor material preferably contains In, Ga, and Zn. The off-state current of a transistor in which an oxide semiconductor is used for a channel formation region is extremely small. Therefore, by forming a memory cell using the transistor, data can be held for a long time.
With the use of multilevel interconnection, a plurality of memory cells included in a memory device are stacked to overlap, and further, the memory cells and a driver circuit for driving the memory cells are stacked to overlap.
An embodiment of the present invention is a memory device including a driver circuit provided over a substrate and a plurality of memory cell arrays which are provided over the driver circuit and driven by the driver circuit. Each of the plurality of memory cell arrays includes a plurality of memory cells arranged in matrix. Each of the plurality of memory cells includes a first transistor including an oxide semiconductor layer, a source electrode, a drain electrode, a first gate insulating layer, and a first gate electrode overlapping with the oxide semiconductor layer with the first gate insulating layer provided therebetween, and a capacitor including one of the source electrode and the drain electrode, the first gate insulating layer, and a conductive layer overlapping with the one of the source electrode and the drain electrode with the first gate insulating layer provided therebetween. The plurality of memory cell arrays is stacked to overlap.
Each of the plurality of memory cell arrays may include a bit line which is electrically connected to the other of the source electrode and the drain electrode of the first transistor, a word line which is electrically connected to the first gate electrode of the first transistor, and a capacitor line which is electrically connected to the conductive layer of the capacitor.
The bit lines of the plurality of memory cell arrays may be electrically connected to each other.
The word lines of the plurality of memory cell arrays may be electrically connected to each other.
The capacitor lines of the plurality of memory cell arrays may be electrically connected to each other.
The bit lines of the two adjacent memory cell arrays of the plurality of memory cell arrays may be arranged so as not to overlap with each other.
The word lines of the two adjacent memory cell arrays of the plurality of memory cell arrays may be arranged so as not to overlap with each other.
The driver circuit can be formed using a second transistor. The second transistor includes a channel formation region that is provided in a substrate including a semiconductor material other than an oxide semiconductor, a pair of impurity regions that are provided so that the channel formation region is sandwiched between the pair of impurity regions, a second gate insulating layer that is provided over the channel formation region, and a second gate electrode that overlaps with the channel formation region and is provided over the second gate insulating layer. Here, one of the pair of impurity regions is a source and the other is a drain.
As another example, the second transistor is provided over an insulating surface and includes a channel formation region that is provided in a semiconductor layer including a semiconductor material other than an oxide semiconductor, a pair of impurity regions that are provided so that the channel formation region is sandwiched between the pair of impurity regions, a second gate insulating layer that overlaps with the channel formation region, and a second gate electrode that is provided to overlap with the channel formation region with the second gate insulating layer provided therebetween. Here, one of the pair of impurity regions is a source and the other is a drain.
Note that the substrate including a semiconductor material is preferably a single crystal semiconductor substrate or an SOI substrate. It is also preferable to use silicon as the semiconductor material other than an oxide semiconductor.
In the above structure, it is preferable that the driver circuit include a bit line driver circuit for driving a bit line and a word line driver circuit for driving a word line; the bit line driver circuit include a first driver circuit and a second driver circuit; each of the first driver circuit and the second driver circuit include a column decoder and a sense amplifier portion; the word line driver circuit include a third driver circuit and a fourth driver circuit; each of the third driver circuit and the fourth driver circuit include a row decoder; and the first to fourth driver circuits be arranged below the plurality of memory cell arrays.
In the above-described structures, the first transistor is formed using an oxide semiconductor; however, the disclosed invention is not limited thereto. A material which can realize the off-state current characteristics equivalent to those of the oxide semiconductor, such as a wide gap material like silicon carbide (specifically, a semiconductor material whose energy gap Eg is larger than 3 eV) may be used.
Since a transistor (first transistor) in which an oxide semiconductor is used for a channel formation region has extremely small off-state current, stored data can be held for an extremely long time by using the transistor. In other words, power consumption can be sufficiently reduced because refresh operation becomes unnecessary or the frequency of refresh operation can be extremely low. Moreover, stored data can be held for a long time even when power is not supplied.
Further, a memory device according to the disclosed invention does not require high voltage for writing data and does not have a problem of deterioration of elements. For example, unlike a conventional nonvolatile memory, it is not necessary to inject and extract electrons into and from a floating gate, and thus a problem such as deterioration of a gate insulating layer does not arise at all. In other words, the semiconductor device according to the disclosed invention does not have a limitation on the number of times data can be rewritten, which is a problem of a conventional nonvolatile memory, and the reliability thereof is drastically improved. Furthermore, since data is written by turning on or off the transistor, high-speed operation can be easily realized.
Further, with the use of multilevel interconnection, a plurality of memory cells included in a memory device is stacked to overlap, and furthermore, the memory cells and a driver circuit for driving the memory cells are stacked to overlap. Thus, memory capacity per unit area can be increased.
For example, in the case where a memory device is formed using only one memory cell array without using multilevel interconnection, the area of a memory cell is 8 F2 to 10 F2 (F is a half pitch determined by a design rule). On the other hand, the area of a memory cell can be reduced to 1 F2 by stacking 8 to 10 memory cell arrays so as to overlap.
Bit lines of the two adjacent memory cell arrays of the plurality of memory cell arrays may be arranged so as not to overlap with each other, so that parasitic capacitance of the bit lines can be reduced and accuracy of reading data can be improved. Further, speed of writing and reading data can be improved. Furthermore, a load on a driver circuit for driving the bit line can be reduced.
Word lines of the two adjacent memory cell arrays of the plurality of memory cell arrays can be arranged so as not to overlap with each other. Thus, parasitic capacitance of the word lines can be reduced and speed of writing and reading data can be improved. Further, a load on a driver circuit for driving the word line can be reduced.
Since a transistor (second transistor) in which a material other than an oxide semiconductor is used for a channel formation region can operate at sufficiently high speed, when it is combined with the transistor (first transistor) in which an oxide semiconductor is used for a channel formation region, a memory device can perform operation (e.g., reading data) at sufficiently high speed. Further, the transistor (second transistor) in which a material other than an oxide semiconductor is used for a channel formation region can favorably realize a variety of driver circuits which are required to operate at high speed.
Furthermore, the area par memory cell array becomes small due to multilevel interconnection by dividing a bit line driver circuit into a first driver circuit and a second driver circuit and dividing a word line driver circuit into a third driver circuit and a fourth driver circuit, so that all the driver circuits can be arranged in a region overlapping with the memory cell array. Thus, a memory device can be downsized.
In the accompanying drawings:
Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings. However, the present invention is not limited to the following description and it is easily understood by those skilled in the art that the mode and details can be variously changed without departing from the scope and spirit of the present invention. Accordingly, the present invention should not be construed as being limited to the description of the embodiments described below. In describing configurations of the present invention with reference to the drawings, the same reference numerals are used in common for the same portions in different drawings. The same hatching pattern is applied to similar parts, and the similar parts are not especially denoted by reference numerals in some cases. In addition, an insulating layer is not illustrated in a top view in some cases.
Note that the position, the size, the range, or the like of each structure illustrated in drawings and the like is not accurately represented in some cases for easy understanding. Therefore, the disclosed invention is not necessarily limited to the position, size, range, or the like as disclosed in the drawings and the like.
In this specification and the like, ordinal numbers such as “first”, “second”, and “third” are used in order to avoid confusion among components, and the terms do not mean limitation of the number of components.
Note that the term “over” or “under” in this specification and the like does not necessarily mean that a component is placed “directly on” or “directly under” another component. For example, the expression “a gate electrode over a gate insulating layer” does not exclude a structure where a component is placed between the gate insulating layer and the gate electrode.
In addition, in this specification and the like, the term such as “electrode” or “wiring” does not limit a function of a component. For example, an “electrode” is sometimes used as part of a “wiring”, and vice versa. Further, the term “electrode” or “wiring” can include the case where a plurality of “electrodes” or “wirings” is formed in an integrated manner.
For example, part of a word line may be used as a first gate electrode of a first transistor and part of a capacitor line may be used as an electrode layer of a capacitor.
Functions of a “source” and a “drain” are sometimes replaced with each other when a transistor of opposite polarity is used or when the direction of current flowing is changed in circuit operation, for example. Therefore, the terms “source” and “drain” can be replaced with each other in this specification and the like.
Note that in this specification and the like, the term “electrically connected” includes the case where components are connected through an object having any electric function. There is no particular limitation on an object having any electric function as long as electric signals can be transmitted and received between components that are connected through the object.
Examples of an “object having any electric function” are a switching element such as a transistor, a resistor, an inductor, a capacitor, and an element with a variety of functions as well as an electrode and a wiring.
A structure of a memory device according to an embodiment of the present invention will be described with reference to
<Structure of Memory Device>
The memory device illustrated in
The memory cell array 201a and the memory cell array 201b are stacked to overlap. Accordingly, memory capacity per unit area can be increased. Although an example in which two memory cell arrays (the memory cell array 201a and the memory cell array 201b) are stacked to overlap is illustrated in
According to an embodiment of the present invention, a plurality of memory cell arrays is stacked to overlap with the use of multilevel interconnection. Here, as compared to the case where a memory cell array is one layer (the case where multilevel interconnection is not used), a method in which the memory cell array is divided and stacked to overlap will be described with reference to schematic views.
<Method for Dividing and Stacking Memory Cell Array>
As illustrated in
According to an embodiment of the present invention, the memory cell array 601 is divided and the divided memory cell arrays are stacked to overlap in order to increase memory capacity per unit area.
As examples of a method for dividing the memory cell array 601 into two parts, methods illustrated in
In the dividing method illustrated in
Note that the method for dividing a memory cell array into two parts is not limited to the methods illustrated in
As examples of a method for dividing the memory cell array 601 into three parts, methods illustrated in
In the dividing method illustrated in
As examples of a method for dividing the memory cell array 601 into four parts, methods illustrated in
In the dividing method illustrated in
Note that the method for dividing a memory cell array is not limited to the methods illustrated in
It is preferable that the memory cell array 601 be divided so that each of the divided memory cell arrays has a horizontal-to-vertical ratio as close to as 1:1. In addition, it is also preferable that the memory cell array 601 be divided so that each of the divided memory cell arrays includes the same number of memory cells. Thus, memory capacity per unit area can be further increased.
For example, in the case where a memory device is formed using only one memory cell array without using multilevel interconnection (corresponding to the case illustrated in
Next, a configuration of each memory cell will be described.
<Configuration of Memory Cell>
In the memory cell 170 illustrated in
The transistor 162 in which an oxide semiconductor is used for a channel formation region has a characteristic of a significantly small off-state current. For that reason, when the transistor 162 is in an off state, a potential of the first terminal of the capacitor 164 (or charge accumulated in the capacitor 164) can be held for an extremely long period. Further, in the transistor 162 in which an oxide semiconductor is used for a channel formation region, a short channel effect is not likely to be caused, which is advantageous.
Next, writing and holding data in the memory cell 170 illustrated in
First, the potential of the word line WL is set to a potential at which the transistor 162 is turned on, and the transistor 162 is turned on. Accordingly, the potential of the bit line BL is supplied to the first terminal of the capacitor 164 (writing). After that, the potential of the word line WL is set to a potential at which the transistor 162 is turned off, so that the transistor 162 is turned off. Thus, the potential of the first terminal of the capacitor 164 is held (holding).
Because the off-state current of the transistor 162 is extremely small, the potential of the first terminal of the capacitor 164 (or charge accumulated in the capacitor 164) can be held for a long time.
Next, reading data will be described. When the transistor 162 is turned on, the bit line BL and the capacitor 164 which are in a floating state are electrically connected to each other, and the charge is redistributed between the bit line BL and the capacitor 164. As a result, the potential of the bit line BL is changed. The amount of change in potential of the bit line BL varies depending on the potential of the first terminal of the capacitor 164 (or charge accumulated in the capacitor 164).
For example, the potential of the bit line BL after charge redistribution is (CB*VB0+C*V)/(CB+C), where V is the potential of the first terminal of the capacitor 164, C is the capacitance of the capacitor 164, CB is the capacitance of the bit line BL (hereinafter also referred to as a bit line capacitance), and VB0 is the potential of the bit line BL before the charge redistribution. Therefore, it can be found that assuming that the memory cell 170 is in either of two states in which the potentials of the first terminal of the capacitor 164 are V1 and V0 (V1>V0), the potential of the bit line BL in the case of holding the potential V1 (=(CB*VB0+C*V1)/(CB+C)) is higher than the potential of the bit line BL in the case of holding the potential V0 (=(CB*VB0+C*V0)/(CB+C)).
Then, by comparing the potential of the bit line BL with a predetermined potential, data can be read.
Thus, the memory cell illustrated in
<Circuit Configuration of Memory Cell Array and Driving Method Thereof>
Next, a circuit diagram of the memory cell array 201 and part of the peripheral circuit is illustrated in
The memory cell array 201 illustrated in
The first driver circuit 211 includes the column decoder 217a and the sense amplifier group 216a, and the sense amplifier group 216a includes sense amplifiers 222(j+1) to 222(n). The column decoder 217a is electrically connected to the sense amplifiers 222(j+1) to 222(n) through column address lines CA(j+1) to CA(n), and the sense amplifiers 222(j+1) to 222(n) are electrically connected to the memory cell array 201 through the bit lines BLa(j+1) to BLa(n) and the bit lines BLb(j+1) to BLb(n). Similarly, the second driver circuit 212 includes the column decoder 217b and the sense amplifier group 216b, and the sense amplifier group 216b includes sense amplifiers 222(1) to 222(j). The column decoder 217b is electrically connected to the sense amplifiers 222(1) to 222(j) through column address lines CA(1) to CA(j), and the sense amplifiers 222(1) to 222(j) are electrically connected to the memory cell array 201 through the bit lines BLa(1) to BLa(j) and the bit lines BLb(1) to BLb(j).
In the sense amplifier illustrated in
In the sense amplifier illustrated in
Next, the case where writing, holding, and reading data is performed on the memory cell array 201 is described with reference to
In the case where data is written to the memory cell 170(1,1) illustrated in
Then, a read circuit, a write circuit, and a latch circuit group included in the fifth driver circuit 215 illustrated in
Next, the word line WL(1) in the first row which is a selected row is activated, so that the transistor 162 of the memory cell 170(1,1) is turned on. Here, the word line WL(1) is supplied with a potential VDDH which is higher than the potential VDD. As a result, the first terminal of the capacitor 164 of the memory cell 170(1,1) is supplied with VDD. After that, the word line WL(1) is deactivated (here, supplied with the potential VSS), so that the transistor 162 of the memory cell 170(1,1) is turned off. In this manner, data “1” can be written to the memory cell 170(1,1). Furthermore, by turning off the transistor 162 of the memory cell 170(1,1), the potential of the first terminal of the capacitor 164 (or charge accumulated in the capacitor 164) is held.
Note that although the case of writing data “1” is described here, the case of writing data “0” is also similar.
Next, the case where data is read from the memory cell 170(1,1) is described with reference to a timing chart in
In order to read data from the memory cell 170(1,1), the potential VDD is applied to the signal line φpc, the bit line BLa(1) and the bit line BLb(1) are precharged, and the potential Vpc is applied to the bit line BLa(1) and the bit line BLb(1). Here, the potential Vpc is VDD/2. Then, the potential VSS is applied to the signal line φpc, and thus, precharge is completed.
Next, the word line WL(1) in the first row which is a selected row is activated, so that the transistor 162 of the memory cell 170(1,1) is turned on. Here, the word line WL(1) is supplied with the potential VDDH which is higher than the potential VDD. As a result, charge is redistributed between the bit line BLa(1) and the capacitor 164 of the memory cell 170(1,1), and the potential of the bit line BLa(1) is slightly increased.
Next, the sense amplifier is activated. Here, by changing the potential applied to the signal line φn from VSS to VDD, the potential VL is applied to the n-channel transistor 408 included in the sense amplifier. As a result, the potential of the bit line BLa(1) is slightly higher than that of the bit line BLb(1), and therefore, the sense amplifier amplifies the difference and decreases the potential of the bit line BLb(1) to the potential VL. Subsequently, by changing the potential applied to the signal line p from VDD to VSS, the potential VH is applied to the p-channel transistor 409 included in the sense amplifier. As a result, the potential of the bit line BLb(1) is equal to the potential VL which is lower than that of the bit line BLa(1), and therefore, the sense amplifier amplifies the difference and increases the potential of the bit line BLa(1) to the potential VH. As a result, the bit line BLa(1) is supplied with the potential VH and the bit line BLb(1) is supplied with the potential VL. In
Next, the signal line CA(1) in the first column which is a selected column is activated. Here, the signal line CA(1) is supplied with the potential VDD. As a result, the bit line BLa(1) and the bit line BLb(1) are electrically connected to the signal line IOa and the signal line IOb, respectively, which are electrically connected to the read circuit, the write circuit, and the latch circuit group of the fifth driver circuit 215. Thus, the potentials of the bit line BLa(1) and the bit line BLb(1) are read.
In this manner, data is read from the memory cell 170(1,1).
After the data stored in the memory cell 170(1,1) is read out to the read circuit, the write circuit, and the latch circuit group, the signal line CA(1) is deactivated (here, supplied with the potential VSS), so that the bit line BLa(1) and the bit line BLb(1) are electrically disconnected from the signal line IOa and the signal line IOb. Then, the word line WL(1) is deactivated (here, supplied with the potential VSS), so that the transistor 162 of the memory cell 170(1,1) is turned off. At this time, data “1” is stored again in the memory cell 170(1,1). After that, the sense amplifier may be deactivated by changing the potential applied to the signal line φn from VDD to VSS and changing the potential applied to the signal line φp from VSS to VDD. The bit line BLa(1) and the bit line BLb(1) may be precharged by applying the potential VDD to the signal line φpc.
In the above manner, data “1” can be read from the memory cell 170(1,1).
Note that although the case of reading data “1” from the memory cell 170(1,1) is described here, a read operation in the case of reading data “0” is also similar. In that case, charge is redistributed between the bit line BLa(1) and the capacitor 164 of the memory cell 170(1,1), and the potential of the bit line BLa(1) is slightly decreased. The sense amplifier amplifies the difference, decreases the potential of the bit line BLa(1) to the potential VL, and increases the potential of the bit line BLb(1) to the potential VH.
What is described above is the circuit configuration of the memory cell array and the driving method thereof.
According to one embodiment of the present invention, a plurality of memory cell arrays 201 is stacked with the use of multilevel interconnection. For example, in the circuit diagram illustrated in
Next, an example of a method for arranging peripheral circuit stacked to overlap with a memory cell array will be described.
<Arrangement of Driver Circuit>
The peripheral circuit 210 illustrated in
As a substrate where the peripheral circuit 210 illustrated in
The address buffer 221 outputs a row address signal to the row decoder 223a and the row decoder 223b, or a column address signal to the column decoder 217a and the column decoder 217b, according to a variety of control signals on an input of an address signal ADR from the outside. The row decoder 223a and the row decoder 223b select a row specified by a row address according to the input row address signal. The column decoder 217a and the column decoder 217b select a column specified by a column address according to the input column address signal.
The sense amplifier groups 216a and 216b are electrically connected to bit lines BL, and detect and amplify the potentials of the bit lines BL.
The fifth driver circuit 215 includes the read circuit, the write circuit, and the latch circuit group, and is electrically connected to the sense amplifier groups 216a and 216b. The read circuit receives an output signal of a sense amplifier of a column specified by a column address as an input signal, and reads out data stored in a memory cell. The write circuit outputs a signal corresponding to data to be written to a bit line BL of a column specified by a column address. The latch circuit group stores data read from a memory cell or data to be written to a memory cell.
The I/O buffer 220 receives data which is input from the outside through a data signal line, and outputs data to the write circuit and the latch circuit group of the fifth driver circuit 215. In addition, the I/O buffer 220 receives data which is stored in the read circuit and the latch circuit group, and outputs data to the outside.
The controller 218 includes a command decoder, the mode register 219, and the like and receives a variety of control signals (e.g., /CS, /RAS, /CAS, and /WE). The command decoder decodes a command that is input by means of the variety of control signals. The mode register 219 is a register for setting an operation mode of a semiconductor device. Data is written to the mode register 219 according to a command and supplied with data to be written thereto by means of an address signal. The controller 218 generates a variety of control signals based on an output of the command decoder, and outputs the control signals to a variety of circuits.
Here, the first driver circuit 211 and the second driver circuit 212 are arranged so as to be symmetrical with respect to the center point 250 of the memory cell array 201a. The third driver circuit 213 and the fourth driver circuit 214 are arranged so as to be symmetrical with respect to the center point 250 of the memory cell array 201a. At this time, the first to fourth circuits 211 to 214 are arranged so that a direction in which circuit elements for different rows are disposed in the third driver circuit 213 and the fourth driver circuit 214 (the horizontal direction in
As illustrated in
Note that although
The number of wirings which electrically connect the first driver circuit 211 and the memory cell array (the memory cell array 201a or the memory cell array 201b in
However, it is preferable that the number of wirings which electrically connect the first drive circuit 211 and the memory cell array (the memory cell array 201a or the memory cell array 201b in
Further, when the number of wirings which electrically connect the first driver circuit 211 and the memory cell array (the memory cell array 201a or the memory cell array 201b in
Although the first driver circuit 211 and the second driver circuit 212 are described here, a similar effect can be obtained with the third driver circuit 213 and the fourth driver circuit 214.
As illustrated in
The first driver circuit 211 and the second driver circuit 212 are each divided and the divided first driver circuits 211 are arranged so as to be symmetrical to the divided second driver circuits 212 with respect to the center point of the memory cell array 201a. The third driver circuit 213 and the fourth driver circuit 214 are each divided and the divided third driver circuits 213 are arranged so as to be symmetrical to the divided fourth driver circuits 214 with respect to the center point of the memory cell array 201a. Accordingly, a wasted region can be eliminated, and therefore, the area of the peripheral circuit 210 can be decreased. Furthermore, the peripheral circuit 210 can be provided under the memory cell array 201a. Thus, the size of the memory device can be reduced. Moreover, by making the area of the memory cell array 201a substantially equal to the area of the peripheral circuit 210, a wasted region can be eliminated. Thus, the area and size of the memory device can be reduced.
Note that although
This embodiment can be implemented in appropriate combination with the configurations described in the other embodiments.
In this embodiment, a structure and a manufacturing method of a memory device according to an embodiment of the present invention will be described with reference to
<Cross-Sectional Structure of Memory Device>
Either an n-channel transistor or a p-channel transistor can be used as the transistor 160 and the transistor 162. Here, both the transistor 160 and the transistor 162 are n-channel transistors in the following description. The technical feature of an embodiment of the present invention is to use a semiconductor material with which off-state current can be sufficiently decreased, such as an oxide semiconductor, for a channel formation region of the transistor 162 so that data can be held. Therefore, it is not necessary to limit a specific structure of the memory device, such as a material of the memory device or a structure of the memory device, to the structure described here.
The transistor 160 includes a channel formation region 116 provided in a substrate 100 including a semiconductor material (such as silicon); impurity regions 120 provided such that the channel formation region 116 is sandwiched therebetween; metal compound regions 124 in contact with the impurity regions 120; a gate insulating layer 108 provided over the channel formation region 116; a gate electrode 110 provided over the gate insulating layer 108; and a source or drain electrode 130a and a source or drain electrode 130b electrically connected to the metal compound regions 124. In addition, an insulating layer 128 is provided so as to cover the transistor 160. The source or drain electrode 130a and the source or drain electrode 130b are electrically connected to the metal compound regions 124 through openings formed in the insulating layer 128. Over the insulating layer 128, an electrode 136a is formed in contact with the source or drain electrode 130a, and an electrode 136b is formed in contact with the source or drain electrode 130b.
Further, an element isolation insulating layer 106 is formed over the substrate 100 so as to surround the transistor 160, and the insulating layer 128 is formed over the transistor 160. Note that in order to realize higher integration, the transistor 160 preferably has a structure without a sidewall insulating layer as illustrated in
The transistor 162 includes an oxide semiconductor layer 144 provided over the insulating layer 128 and the like; an electrode 142a and an electrode 142b which are electrically connected to the oxide semiconductor layer 144; a gate insulating layer 146 covering the oxide semiconductor layer 144, the electrode 142a, and the electrode 142b; and an electrode 148a provided over the gate insulating layer 146 so as to overlap with the oxide semiconductor layer 144. The electrode 148a serves as a gate electrode of the transistor 162. One of the electrode 142a and the electrode 142b serves as a drain electrode of the transistor 162 and the other serves as a source electrode.
Here, an oxide semiconductor layer used for a transistor, such as the oxide semiconductor layer 144, is preferably an oxide semiconductor layer which is purified by sufficiently removing an impurity such as hydrogen therefrom and then sufficiently supplying oxygen thereto. Specifically, the hydrogen concentration in the oxide semiconductor layer is 5×1019 atoms/cm3 or less, preferably 5×1018 atoms/cm3 or less, more preferably 5×1017 atoms/cm3 or less, for example. Note that the above hydrogen concentration in the oxide semiconductor layer is measured by secondary ion mass spectrometry (SIMS). The concentration of carriers in the oxide semiconductor layer, in which hydrogen is reduced to a sufficiently low concentration and defect states in an energy gap due to oxygen deficiency are reduced by sufficiently supplying oxygen as described above, is less than 1×1012/cm3, preferably less than 1×1011/cm3, more preferably less than 1.45×1010/cm3. For example, the off-state current (per unit channel width (1 μm), here) at room temperature (25° C.) is 100 zA (1 zA (zeptoampere) is 1×10−21 A) or less, preferably 10 zA or less. In this manner, by using an i-type (intrinsic) or substantially i-type oxide semiconductor, a transistor (the transistor 162) which has extremely favorable off-state current characteristics can be obtained.
Further, it is preferable that the concentration of an alkali metal and an alkaline earth metal in the oxide semiconductor layer 144 be sufficiently reduced. As for the concentration of an alkali metal or an alkaline earth metal measured by SIMS, for example, the concentration of Na is 5×1016 cm−3 or lower, preferably 1×1016 cm−3 or lower, more preferably 1×1015 cm−3 or lower; the concentration of Li is 5×1015 cm−3 or lower, preferably 1×1015 cm−3 or lower; or the concentration of K is 5×1015 cm−3 or lower, preferably 1×1015 cm−3 or lower.
Note that it has been pointed out that an oxide semiconductor is insensitive to impurities, there is no problem when a considerable amount of metal impurities is contained in the film, and therefore, soda-lime glass which contains a large amount of alkali metal such as sodium and is inexpensive can also be used (Kamiya, Nomura, and Hosono, “Carrier Transport Properties and Electronic Structures of Amorphous Oxide Semiconductors: The present status”, KOTAI BUTSURI (SOLID STATE PHYSICS), 2009, Vol. 44, pp. 621-633). But such consideration is not appropriate. An alkali metal and an alkaline earth metal are adverse impurities for the oxide semiconductor and are preferably contained as little as possible. An alkali metal, in particular, Na diffuses into an oxide and becomes Na+ when an insulating film in contact with the oxide semiconductor is an oxide. In addition, Na cuts a bond between metal and oxygen or enters the bond in the oxide semiconductor. As a result, deterioration of transistor characteristics (e.g., the shift of a threshold value to the negative side (causing the transistor to be normally on) or a decrease in mobility) is caused. In addition, this also causes variation in the characteristics. Such a problem is significant especially in the case where the hydrogen concentration in the oxide semiconductor is extremely low. Therefore, the concentration of an alkali metal is strongly required to set to the above value in the case where the hydrogen concentration in the oxide semiconductor is lower than or equal to 5×1019 cm−3, particularly lower than or equal to 5×1018 cm−3.
Note that the oxide semiconductor layer 144 may exhibit slight (weak) p-type conductivity by adding an impurity imparting p-type conductivity such as tin (Sn) to the oxide semiconductor layer 144. The oxide semiconductor layer which is purified as described above becomes i-type (intrinsic) or substantially i-type, so that the oxide semiconductor layer 144 which exhibits weak p-type conductivity can be obtained by adding a small amount of an impurity for controlling valence electrons. Thus, the threshold voltage of the transistor 162 can be slightly shifted toward the positive side. Accordingly, the transistor 162 is prevented from becoming normally on and off-state current can be further reduced. Alternatively, in order to prevent the transistor 162 from becoming normally on, a second gate electrode may be provided on a surface of the oxide semiconductor layer 144 of the transistor 162, which is opposite to the surface provided with the gate electrode (the electrode 148a), with an insulating layer provided therebetween so that the threshold voltage is controlled by the second gate electrode.
Although the oxide semiconductor layer processed in an island shape is used for the transistor 162 in order to suppress leakage among elements due to miniaturization, an oxide semiconductor layer not processed in an island shape may be used. When an oxide semiconductor layer is not processed in an island shape, the oxide semiconductor layer can be prevented from being contaminated by etching during processing.
A capacitor 164 includes the electrode 142b, the gate insulating layer 146, and a conductive layer 148b. That is, the electrode 142b functions as one electrode of the capacitor 164, and the conductive layer 148b functions as the other electrode of the capacitor 164. With such a structure, capacitance can be sufficiently secured. When the oxide semiconductor layer 144 and the gate insulating layer 146 are stacked, insulation between the electrode 142b and the conductive layer 148b can be sufficiently secured. Furthermore, in the case where no capacitor is needed, a structure in which the capacitor 164 is not provided is also possible.
Note that in the transistor 162 and the capacitor 164, the electrode 142a and the electrode 142b preferably have tapered end portions. When the electrode 142a and the electrode 142b have tapered end portions, coverage of the electrode 142a and the electrode 142b with the gate insulating layer 146 can be improved and disconnection of the gate insulating layer 146 can be prevented. Here, the taper angle is in the range of 30° to 60°, for example. Note that the “taper angle” means an angle formed by the side surface and the bottom surface of a layer having a tapered shape (for example, the electrode 142a) when observed from a cross section thereof (a plane perpendicular to the substrate surface).
An insulating layer 150 and an insulating layer 152 are provided over the transistor 162 and the capacitor 164. An electrode 154a is provided in an opening formed in the gate insulating layer 146, the insulating layer 150, the insulating layer 152, and the like, and a wiring 156 which is electrically connected to the electrode 154a is formed over the insulating layer 152. The wiring 156 is a wiring for electrically connecting one memory cell to another memory cell in each memory cell array (memory cell arrays arranged in the same layer), and can be a bit line, for example. Further, the electrode 148a is a wiring which extends in a direction of C1-C2 and electrically connects one memory cell to another memory cell in each memory cell array (memory cell arrays arranged in the same layer), and can be a word line, for example (see
The wiring 156 included in the memory cell array 201a is electrically connected to an electrode 136c through an electrode 502a, an electrode 501a, and an electrode 126. Thus, the peripheral circuit 210 in the lower layer and a bit line of the memory cell array 201a in the upper layer can be electrically connected to each other. Although the case where the electrode 501a is electrically connected to the electrode 136c through the electrode 126 is illustrated in
The electrode 148a is electrically connected to an electrode 556 through an electrode 557. Thus, the peripheral circuit 210 in the lower layer and a word line of the memory cell array 201a in the upper layer can be electrically connected to each other. Although the case where the electrode 148a is electrically connected to the electrode 556 through the electrode 557 is illustrated in
Although not illustrated, like the word line of the memory cell array 201a, the conductive layer 148b serving as a capacitor line can also be electrically connected to the peripheral circuit 210 in the lower layer.
Next, a method for electrically connecting wirings of a plurality of memory cell arrays is described.
The case where the bit line included in the memory cell array 201a is electrically connected to the bit line included in the memory cell array 201b is described with reference to
The wiring 156 serving as the bit line included in the memory cell array 201a and the wiring 156 serving as the bit line included in the memory cell array 201b are electrically connected to each other through an electrode 500, an electrode 501b, and an electrode 502b. In
Although an example in which the position where an electrode for electrically connecting the bit line of the memory cell array 201a to the peripheral circuit 210 is formed and the position where an electrode for electrically connecting the bit line of the memory cell array 201a to the bit line of the memory cell array 201b are greatly different in the plane layout is illustrated in
The case where the word line included in the memory cell array 201a is electrically connected to the word line included in the memory cell array 201b is described with reference to
The electrode 148a serving as the word line included in the memory cell array 201a and the electrode 148a serving as the word line included in the memory cell array 201b are electrically connected to each other through an electrode 551, an electrode 552, and an electrode 553. In
Although an example in which the position where an electrode for electrically connecting the word line of the memory cell array 201a to the peripheral circuit 210 is formed and the position where an electrode for electrically connecting the word line of the memory cell array 201a to the word line of the memory cell array 201b are greatly different in the plane layout is illustrated in
Although not illustrated, capacitor lines of the plurality of memory cell arrays can be electrically connected to each other in a manner similar to that of the word lines.
In the memory device illustrated in
The transistor 160 includes a semiconductor material other than an oxide semiconductor in a channel formation region. The semiconductor material other than an oxide semiconductor may be, for example, silicon, germanium, silicon germanium, silicon carbide, gallium arsenide, or the like and is preferably a single crystal semiconductor. Alternatively, an organic semiconductor material or the like may be used. A transistor including such a semiconductor material can operate at sufficiently high speed. Therefore, a transistor including a material other than an oxide semiconductor can favorably realize a variety of circuits (e.g., a logic circuit or a driver circuit) which needs to operate at high speed.
On the other hand, the transistor 162 includes an oxide semiconductor material in a channel formation region. A transistor including an oxide semiconductor material disclosed in this specification and the like can realize an extremely small off-state current. Owing to this feature, the memory cell 170 can hold stored data for an extremely long time. In other words, refresh operation becomes unnecessary or the frequency of the refresh operation can be extremely lowered, which leads to a sufficient reduction in power consumption. Moreover, stored data can be held for a long period even when power is not supplied. Further, when a normally-off (enhancement) transistor is used as the transistor 162, and power is not supplied, a ground potential may be input to the gate of the transistor 162. With that structure, the transistor 162 can remain off and stored data can be kept held even when power is not supplied.
Further, the memory cell 170 does not require high voltage for writing data and does not have the problem of deterioration of elements. For example, unlike a conventional nonvolatile memory, it is not necessary to inject and extract electrons into and from a floating gate, and thus a problem such as deterioration of a gate insulating layer does not arise at all. That is, the memory cell 170 does not have a limitation on the number of times data can be rewritten, which is a problem of a conventional nonvolatile memory, and the reliability thereof is drastically improved. Furthermore, since data is written by turning on or off the transistor 162, high-speed operation can be easily realized. Additionally, there is an advantage in that operation for erasing data is not needed.
A memory device having a novel feature can be realized by being provided with both a peripheral circuit such as a driver circuit including a transistor including a material other than an oxide semiconductor (in other words, a transistor capable of operating at sufficiently high speed) and a memory circuit including a transistor including an oxide semiconductor (in a broader sense, a transistor whose off-state current is sufficiently small).
A driver circuit and a control circuit included in the peripheral circuit 210 illustrated in
<Cross-Sectional Structure and Planar Structure of Memory Cell>
Since the structure of the memory cell illustrated in
In a transistor 162 illustrated in
A transistor 162 illustrated in
A transistor 162 illustrated in
Although
In a transistor 162 illustrated in
An insulating layer 150 and an insulating layer 151 are provided over the transistor 162 and the capacitor 164. The insulating layer 152 in
A transistor 162 illustrated in
Moreover, the transistor 162 may have a dual-gate structure including two gate electrodes positioned above and below a channel formation region with gate insulating layers provided therebetween.
The transistor 162 illustrated in
Although the structure in which the capacitor 164 includes the electrode 148b, the gate insulating layer 146, and the electrode 142b is illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
For example, as illustrated in
Note that any of the structures of the capacitor 164 of the memory cell illustrated in
As illustrated in
In the memory cell 170c and the memory cell 170d in
In the memory cell 170c and the memory cell 170d in
Further, an example in which the memory cell illustrated in
Note that memory cells to be stacked are not limited to the memory cell illustrated in
<Method for Manufacturing Memory Cell Array>
Next, a method for manufacturing a memory cell array is described with reference to
First, the oxide semiconductor layer 144 is formed by forming an oxide semiconductor layer over the insulating layer 140 and then by processing the oxide semiconductor layer (see
The insulating layer 140 is formed using a material including an inorganic insulating material such as silicon oxide, silicon oxynitride, silicon nitride oxide, silicon nitride, or aluminum oxide. It is preferable to use a low dielectric constant (low-k) material for the insulating layer 140 because capacitance due to overlap of electrodes or wirings can be sufficiently reduced. Note that a porous insulating layer with any of the above materials may be employed as the insulating layer 140. A porous insulating layer has a lower dielectric constant than an insulating layer with high density, and thus allows a further reduction in capacitance generated by electrodes or wirings. Alternatively, the insulating layer 140 can be formed using an organic insulating material such as polyimide or acrylic. The insulating layer 140 can be formed to have a single-layer structure or a stacked-layer structure using the above-described material. In this embodiment, the case of using silicon oxide for the insulating layer 140 is described.
An oxide semiconductor used for the oxide semiconductor layer 144 preferably contains at least indium (In) or zinc (Zn). It is particularly preferable that In and Zn be contained. As a stabilizer for reducing change in electrical characteristics of a transistor including the oxide semiconductor, gallium (Ga) is preferably additionally contained. Tin (Sn) is preferably contained as a stabilizer. Hafnium (Hf) is preferably contained as a stabilizer. Aluminum (Al) is preferably contained as a stabilizer.
As another stabilizer, one or more lanthanoids which include lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu) may be contained.
For the oxide semiconductor layer 144, for example, an indium oxide, a tin oxide, a zinc oxide, a two-component metal oxide such as an In—Zn-based oxide, a Sn—Zn-based oxide, an Al—Zn-based oxide, a Zn—Mg-based oxide, a Sn—Mg-based oxide, an In—Mg-based oxide, or an In—Ga-based oxide, a three-component metal oxide such as an In—Ga—Zn-based oxide (also referred to as IGZO), an In—Al—Zn-based oxide, an In—Sn—Zn-based oxide, a Sn—Ga—Zn-based oxide, an Al—Ga—Zn-based oxide, a Sn—Al—Zn-based oxide, an In—Hf—Zn-based oxide, an In—La—Zn-based oxide, an In—Ce—Zn-based oxide, an In—Pr—Zn-based oxide, an In—Nd—Zn-based oxide, an In—Sm—Zn-based oxide, an In—Eu—Zn-based oxide, an In—Gd—Zn-based oxide, an In—Tb—Zn-based oxide, an In—Dy—Zn-based oxide, an In—Ho—Zn-based oxide, an In—Er—Zn-based oxide, an In—Tm—Zn-based oxide, an In—Yb—Zn-based oxide, or an In—Lu—Zn-based oxide, or a four-component metal oxide such as an In—Sn—Ga—Zn-based oxide, an In—Hf—Ga—Zn-based oxide, an In—Al—Ga—Zn-based oxide, an In—Sn—Al—Zn-based oxide, an In—Sn—Hf—Zn-based oxide, or an In—Hf—Al—Zn-based oxide can be used.
Note that here, for example, an “In—Ga—Zn-based oxide” means an oxide containing In, Ga, and Zn as its main components and there is no particular limitation on the ratio of In:Ga:Zn. Further, a metal element in addition to In, Ga, and Zn may be contained.
The oxide semiconductor layer 144 may be formed using a material represented by the chemical formula, InMO3(ZnO)m (m>0, where m is not an integer). Note that M represents one or more metal elements selected from Ga, Fe, Mn, and Co. Alternatively, a material represented by In3SnO5(ZnO)n (n>0, where n is an integer) may be used as an oxide semiconductor.
For example, an In—Ga—Zn-based oxide with an atomic ratio of In:Ga:Zn=1:1:1 (=1/3:1/3:1/3) or In:Ga:Zn=2:2:1 (=2/5:2/5:1/5), or an oxide with an atomic ratio close to the above atomic ratios can be used. Alternatively, an In—Sn—Zn-based oxide with an atomic ratio of In:Sn:Zn=1:1:1 (=1/3:1/3:1/3), In:Sn:Zn=2:1:3 (=1/3:1/6:1/2), or In:Sn:Zn=2:1:5 (=1/4:1/8:5/8), or an oxide with an atomic ratio close to the above atomic ratios may be used.
However, the composition is not limited to those described above, and a material having an appropriate composition may be used in accordance with necessary semiconductor characteristics (such as mobility, threshold voltage, and variation). In order to obtain necessary semiconductor characteristics, it is preferable that the carrier density, the impurity concentration, the defect density, the atomic ratio of a metal element to oxygen, the interatomic distance, the density, and the like be set as appropriate.
For example, with the In—Sn—Zn-based oxide, a high mobility can be relatively easily obtained. However, the mobility can be increased by reducing the defect density in the bulk also in the case of using the In—Ga—Zn-based oxide.
Note that for example, the expression “the composition of an oxide including In, Ga, and Zn at the atomic ratio, In:Ga:Zn=a:b:c (a+b+c=1), is in the neighborhood of the composition of an oxide including In, Ga, and Zn at the atomic ratio, In:Ga:Zn=A:B:C (A+B+C=1)” means that a, b, and c satisfy the following relation: (a−A)2+(b−B)2+(c−C)2≦r2, and r may be 0.05, for example. The same applies to other oxides.
The oxide semiconductor layer 144 may be either single crystal or non-single-crystal. In the latter case, the oxide semiconductor layer 144 may be either amorphous or polycrystalline. Further, the oxide semiconductor may have either an amorphous structure including a crystalline portion or a non-amorphous structure.
An amorphous oxide semiconductor can have a flat surface with relative ease; therefore, when a transistor is manufactured with the use of the oxide semiconductor, interface scattering can be reduced, and relatively high mobility can be obtained with relative ease.
In a crystalline oxide semiconductor, defects in the bulk can be further reduced and when a surface flatness is improved, mobility higher than that of an amorphous oxide semiconductor can be obtained. In order to improve the surface flatness, the oxide semiconductor is preferably formed over a flat surface. Specifically, the oxide semiconductor is preferably formed over a surface with an average surface roughness (Ra) of less than or equal to 1 nm, preferably less than or equal to 0.3 nm, more preferably less than or equal to 0.1 nm.
Note that Ra is obtained by three-dimensionally expanding centerline average roughness that is defined by JIS B 0601 so as to be able to be applied to a surface. Ra can be expressed as an “average value of the absolute values of deviations from a reference surface to a specific surface” and is defined by the following formula.
Note that, in the above formula, S0 represents the area of a measurement surface (a rectangular region which is defined by four points represented by the coordinates (x1,y1), (x1,y2), (x2,y1), and (x2,y2)), and Z0 represents average height of a measurement surface. Ra can be measured using an atomic force microscope (AFM).
The thickness of the oxide semiconductor layer 144 is preferably greater than or equal to 3 nm and less than or equal to 30 nm. This is because the transistor might be normally on when the oxide semiconductor layer is too thick (e.g., when the thickness is greater than or equal to 50 nm).
The oxide semiconductor layer 144 is preferably formed by a method in which impurities such as hydrogen, water, a hydroxyl group, or hydride do not enter the oxide semiconductor layer 144. For example, the oxide semiconductor layer can be formed by a sputtering method or the like.
In this embodiment, the oxide semiconductor layer 144 is formed by a sputtering method with the use of an In—Ga—Zn—O-based oxide target.
As an In—Ga—Zn—O-based oxide target, for example, an oxide target having a composition ratio of In2O3:Ga2O3:ZnO=1:1:1 [molar ratio] can be used. Note that it is not necessary to limit the material and the composition ratio of the target to the above. For example, an oxide target having a composition ratio of In2O3:Ga2O3:ZnO=1:1:2 [molar ratio] can be used.
Further, in the case where an In—Sn—Zn-based oxide which is referred to as ITZO is formed, a target which has an atomic ratio of In:Sn:Zn of 1:2:2, 2:1:3, 1:1:1, 20:45:35, or the like is used.
The filling rate of the oxide target is greater than or equal to 90% and less than or equal to 100%, preferably greater than or equal to 95% and less than or equal to 99.9%. This is because, with the use of the metal oxide target with a high filling rate, a dense oxide semiconductor layer can be formed.
A film formation atmosphere may be a rare gas (typically, argon) atmosphere, an oxygen atmosphere, or a mixed atmosphere containing a rare gas and oxygen. An atmosphere of a high-purity gas from which impurities such as hydrogen, water, a hydroxyl group, or hydride are sufficiently removed is preferable, in order to prevent hydrogen, water, a hydroxyl group, hydride, or the like from entering the oxide semiconductor layer.
For example, the oxide semiconductor layer 144 can be formed as follows.
First, the substrate is held in a film formation chamber which is kept under reduced pressure, and is then heated so that the substrate temperature reaches a temperature higher than 200° C. and lower than or equal to 500° C., preferably higher than 300° C. and lower than or equal to 500° C., more preferably higher than or equal to 350° C. and lower than or equal to 450° C.
Then, a high-purity gas from which impurities such as hydrogen, water, a hydroxyl group, or hydride are sufficiently removed is introduced into the film formation chamber from which remaining moisture is being removed, and the oxide semiconductor layer is formed over the substrate with the use of the target. To remove moisture remaining in the film formation chamber, an entrapment vacuum pump such as a cryopump, an ion pump, or a titanium sublimation pump is desirably used as an evacuation unit. Further, an evacuation unit may be a turbo pump provided with a cold trap. In the film formation chamber which is evacuated with a cryopump, for example, impurities such as hydrogen, water, a hydroxyl group, or hydride (preferably, also a compound containing a carbon atom) are removed, whereby the concentration of impurities such as hydrogen, water, a hydroxyl group, or hydride in the oxide semiconductor layer formed in the film formation chamber can be reduced.
In the case where the substrate temperature is low (for example, lower than or equal to 100° C.) during film formation, a substance containing a hydrogen atom might enter the oxide semiconductor; thus, it is preferable that the substrate be heated at a temperature in the above range. When the oxide semiconductor layer is formed with the substrate heated at the temperature described above, since the substrate temperature is high, hydrogen bonds are cut by heat and a substance containing a hydrogen atom is less likely to be taken into the oxide semiconductor layer. Therefore, when the oxide semiconductor layer is formed with the substrate heated at the temperature described above, the concentration of impurities such as hydrogen, water, a hydroxyl group, or hydride in the oxide semiconductor layer can be sufficiently reduced. Moreover, damage due to sputtering can be reduced.
As an example of film formation conditions, the following conditions are employed: the distance between the substrate and the target is 60 mm; the pressure is 0.4 Pa; the direct-current (DC) power is 0.5 kW; the substrate temperature is 400° C.; and the film formation atmosphere is an oxygen atmosphere (the proportion of the oxygen flow rate is 100%). Note that a pulse direct-current power source is preferable because powder substances (also referred to as particles or dust) generated in film formation can be reduced and the film thickness can be uniform.
Note that before the oxide semiconductor layer is formed by a sputtering method, powder substances (also referred to as particles or dust) attached to a formation surface of the oxide semiconductor layer are preferably removed by reverse sputtering in which an argon gas is introduced and plasma is generated. The reverse sputtering refers to a method in which voltage is applied to a substrate to generate plasma in the vicinity of the substrate to modify a surface on the substrate side. Note that instead of argon, a gas of nitrogen, helium, oxygen, or the like may be used.
The oxide semiconductor layer 144 is formed by processing an oxide semiconductor layer. The oxide semiconductor layer can be processed by forming a mask having a desired shape over the oxide semiconductor layer and by etching the oxide semiconductor layer. The mask may be formed by a method such as photolithography. Alternatively, a method such as an inkjet method may be used to form the mask. For the etching of the oxide semiconductor layer, either dry etching or wet etching may be employed. It is needless to say that both of them may be employed in combination.
After that, heat treatment (first heat treatment) may be performed on the oxide semiconductor layer 144. The heat treatment can further remove the substance containing a hydrogen atom from the oxide semiconductor layer 144. The heat treatment is performed in an inert gas atmosphere at a temperature higher than or equal to 250° C. and lower than or equal to 700° C., preferably higher than or equal to 450° C. and lower than or equal to 600° C., or lower than a strain point of the substrate. The inert gas atmosphere is preferably an atmosphere which contains nitrogen or a rare gas (e.g., helium, neon, or argon) as its main component and does not contain water, hydrogen, or the like. For example, the purity of nitrogen or a rare gas such as helium, neon, or argon introduced into a heat treatment apparatus is set to 6N (99.9999%) or more, preferably 7N (99.99999%) or more (i.e., the impurity concentration is 1 ppm or less, preferably 0.1 ppm or less).
For example, after an object to be processed is introduced into an electric furnace including a resistance heater or the like, the heat treatment can be performed at 450° C. for one hour in a nitrogen atmosphere. The oxide semiconductor layer 144 is not exposed to the air during the heat treatment so that entry of water or hydrogen can be prevented.
Impurities are reduced by the heat treatment, so that a transistor with extremely excellent characteristics can be realized.
Note that the oxide semiconductor layer 144 may exhibit slight (weak) p-type conductivity by adding an impurity imparting p-type conductivity such as tin (Sn) to the oxide semiconductor layer 144. The oxide semiconductor layer 144 which exhibits weak p-type conductivity can be obtained by adding a small amount of an impurity for controlling valence electrons to the oxide semiconductor layer 144 which is purified as described above. Thus, the threshold voltage of the transistor 162 can be slightly shifted toward the positive side. Accordingly, the transistor 162 is prevented from becoming normally on and off-state current can be further reduced.
The above heat treatment can also be referred to as dehydration treatment, dehydrogenation treatment, or the like because it has the effect of removing hydrogen, water, or the like. The heat treatment can be performed, for example, before the oxide semiconductor layer is processed into an island shape or after the gate insulating film is formed. Such dehydration treatment or dehydrogenation treatment may be conducted once or plural times.
Next, the electrodes 142a and 142b are formed by forming a conductive layer used for forming source and drain electrodes (including a wiring formed using the same layer as the source and drain electrodes) over the oxide semiconductor layer 144 and the like and by processing the conductive layer (see
The conductive layer can be formed by a PVD method or a CVD method. As a material of the conductive layer, an element selected from aluminum, chromium, copper, tantalum, titanium, molybdenum, and tungsten, an alloy including any of these elements as a component, or the like can be used. A material including one of manganese, magnesium, zirconium, beryllium, neodymium, and scandium or a combination of a plurality of these elements may be used.
The conductive layer may have a single-layer structure or a stacked-layer structure including two or more layers. For example, the conductive layer may have a single-layer structure of a titanium film or a titanium nitride film, a single-layer structure of an aluminum film including silicon, a two-layer structure in which a titanium film is stacked over an aluminum film, a two-layer structure in which a titanium film is stacked over a titanium nitride film, a three-layer structure in which a titanium film, an aluminum film, and a titanium film are stacked in this order, or the like. Note that in the case where the conductive layer has a single-layer structure of a titanium film or a titanium nitride film, there is an advantage that the conductive layer can be easily processed into the electrodes 142a and 142b having tapered shapes.
The conductive layer may be formed using a conductive metal oxide. As the conductive metal oxide, indium oxide (In2O3), tin oxide (SnO2), zinc oxide (ZnO), indium oxide-tin oxide alloy (In2O3—SnO2, which is abbreviated to ITO in some cases), indium oxide-zinc oxide alloy (In2O3—ZnO), or any of these metal oxide materials including silicon or silicon oxide can be used.
The conductive layer is preferably etched such that the electrodes 142a and 142b are formed to have tapered end portions. Here, the taper angle is in the range of 30° to 60°, for example. When the electrodes 142a and 142b are formed by etching so as to have tapered end portions, coverage of the electrodes 142a and 142b with the gate insulating layer 146 which is formed later can be improved and disconnection of the gate insulating layer 146 can be prevented.
The channel length (L) of the transistor in the upper portion is determined by a distance between lower edge portions of the electrode 142a and the electrode 142b. Note that for light exposure for forming a mask in the case of manufacturing a transistor with a channel length (L) of less than 25 nm, light exposure is preferably performed with extreme ultraviolet rays whose wavelength is several nanometers to several tens of nanometers, which is extremely short. The resolution of light exposure with extreme ultraviolet rays is high and the focal depth is large. For these reasons, the channel length (L) of the transistor to be formed later can be set in the range of 10 nm to 1000 nm (1 μm), and the circuit can operate at higher speed. In addition, power consumption of the memory device can be reduced by miniaturization.
Next, the gate insulating layer 146 is formed so as to cover the electrodes 142a and 142b and to be in contact with part of the oxide semiconductor layer 144 (see
The gate insulating layer 146 can be formed by a CVD method, a sputtering method, or the like. The gate insulating layer 146 is preferably formed so as to contain silicon oxide, silicon nitride, silicon oxynitride, gallium oxide, aluminum oxide, tantalum oxide, hafnium oxide, yttrium oxide, hafnium silicate (HfSixOy (x>0, y>0)), hafnium silicate (HfSixOy (x>0, y>0)) to which nitrogen is added, hafnium aluminate (HfAlxOy (x>0, y>0)) to which nitrogen is added, or the like. The gate insulating layer 146 may have a single-layer structure or a stacked-layer structure in which these materials are combined. There is no particular limitation on the thickness of the gate insulating layer 146; the thickness is preferably small in order to ensure the operation of the transistor when the memory device is miniaturized. For example, in the case of using silicon oxide, the thickness can be in the range of 1 nm to 100 nm, preferably 10 nm to 50 nm.
When the gate insulating layer is thin as described above, gate leakage due to a tunneling effect or the like becomes a problem. In order to solve the problem of gate leakage, the gate insulating layer 146 may be formed using a high dielectric constant (high-k) material such as hafnium oxide, tantalum oxide, yttrium oxide, hafnium silicate (HfSixOy (x>0, y>0)), hafnium silicate (HfSixOy (x>0, y>0)) to which nitrogen is added, hafnium aluminate (HfAlxOy (x>0, y>0)) to which nitrogen is added. The use of a high-k material for the gate insulating layer 146 makes it possible to increase the thickness in order to suppress gate leakage as well as ensuring electrical properties. Note that a stacked-layer structure of a film including a high-k material and a film including any of silicon oxide, silicon nitride, silicon oxynitride, silicon nitride oxide, aluminum oxide, and the like may also be employed.
Further, the insulating layer in contact with the oxide semiconductor layer 144 (in this embodiment, the insulating layer 140 and the gate insulating layer 146) may be formed using an insulating material containing a Group 13 element and oxygen. Many oxide semiconductor materials contain a Group 13 element, and thus, an insulating material containing a Group 13 element works well with the oxide semiconductor. By using such an insulating material for the insulating layer in contact with the oxide semiconductor, an interface with the oxide semiconductor layer can be kept in a favorable state.
Here, an insulating material containing a Group 13 element refers to an insulating material containing one or more Group 13 elements. As an example of the insulating material containing a Group 13 element, gallium oxide, aluminum oxide, aluminum gallium oxide, gallium aluminum oxide, or the like can be given. Here, aluminum gallium oxide refers to a material in which the amount of aluminum is larger than that of gallium in atomic percent, and gallium aluminum oxide refers to a material in which the amount of gallium is larger than or equal to that of aluminum in atomic percent.
For example, in the case of forming a gate insulating layer in contact with an oxide semiconductor layer containing gallium, a material containing gallium oxide may be used for a gate insulating layer, so that favorable characteristics can be kept at the interface between the oxide semiconductor layer and the gate insulating layer. When the oxide semiconductor layer and the insulating layer containing gallium oxide are provided in contact with each other, pile-up of hydrogen at the interface between the oxide semiconductor layer and the insulating layer can be suppressed, for example. Note that a similar effect can be obtained in the case where an element belonging to the same group as a constituent element of the oxide semiconductor is used for an insulating layer. For example, it is effective to form an insulating layer with the use of a material containing aluminum oxide. Note that aluminum oxide has a property of not easily transmitting water. Thus, it is preferable to use a material containing aluminum oxide in terms of preventing entry of water into the oxide semiconductor layer.
The insulating material of the insulating layer in contact with the oxide semiconductor layer 144 is preferably made to contain oxygen in a proportion higher than that in the stoichiometric proportion by heat treatment in an oxygen atmosphere or by oxygen doping. “Oxygen doping” refers to adding oxygen into a bulk. Note that the term “bulk” is used in order to clarify that oxygen is added not only to a surface of a thin film but also to the inside of the thin film. In addition, “oxygen doping” includes oxygen plasma doping in which oxygen plasma is added to a bulk. The oxygen doping may be performed by an ion implantation method or an ion doping method.
For example, in the case where the insulating layer in contact with the oxide semiconductor layer 144 is formed using gallium oxide, the composition of gallium oxide can be set to be Ga2Ox (x=3+α, 0<α<1) by heat treatment in an oxygen atmosphere or by oxygen doping. In the case where the insulating layer in contact with the oxide semiconductor layer 144 is formed using aluminum oxide, the composition of aluminum oxide can be set to be Al2Ox (x=3+α, 0<α<1) by heat treatment in an oxygen atmosphere or by oxygen doping. In the case where the insulating layer in contact with the oxide semiconductor layer 144 is formed using gallium aluminum oxide (aluminum gallium oxide), the composition of gallium aluminum oxide (aluminum gallium oxide) can be set to be GaxAl2-xO3+α (0<x<2, 0<α<1) by heat treatment in an oxygen atmosphere or by oxygen doping.
By oxygen doping or the like, an insulating layer which has a region where the proportion of oxygen is higher than that in the stoichiometric proportion can be formed. When the insulating layer having such a region is in contact with the oxide semiconductor layer, excess oxygen in the insulating layer is supplied to the oxide semiconductor layer, and oxygen deficiency in the oxide semiconductor layer or at an interface between the oxide semiconductor layer and the insulating layer can be reduced. Thus, the oxide semiconductor layer can be an i-type or substantially i-type oxide semiconductor.
Note that the insulating layer having a region where the proportion of oxygen is higher than that in the stoichiometric proportion may be applied to the insulating layer 140 serving as a base film for the oxide semiconductor layer 144 instead of the gate insulating layer 146, or may be applied to both the gate insulating layer 146 and the base insulating layer 140.
After the gate insulating layer 146 is formed, second heat treatment is preferably performed in an inert gas atmosphere or an oxygen atmosphere. The temperature of the heat treatment is set in the range of 200° C. to 450° C., preferably 250° C. to 350° C. For example, the heat treatment may be performed at 250° C. for one hour in a nitrogen atmosphere. By the second heat treatment, variation in electrical characteristics of the transistor can be reduced. Further, in the case where the gate insulating layer 146 includes oxygen, oxygen can be supplied to the oxide semiconductor layer 144 to cover oxygen deficiency in the oxide semiconductor layer 144, so that an i-type (intrinsic semiconductor) or substantially i-type oxide semiconductor layer can also be formed.
Note that the second heat treatment is performed in this embodiment after the gate insulating layer 146 is formed; there is no limitation on the timing of the second heat treatment. For example, the second heat treatment may be performed after the gate electrode is formed. Alternatively, the first heat treatment and the second heat treatment may be performed in succession, the first heat treatment may also serve as the second heat treatment, or the second heat treatment may also serve as the first heat treatment.
By performing at least one of the first heat treatment and the second heat treatment as described above, the oxide semiconductor layer 144 can be purified so as to contain a substance including a hydrogen atom as little as possible.
Next, a conductive layer for forming a gate electrode (including a wiring formed using the same layer as the gate electrode) is formed and is processed, so that the electrode 148a and the conductive layer 148b are formed (see
The electrode 148a and the conductive layer 148b can be formed using a metal material such as molybdenum, titanium, tantalum, tungsten, aluminum, copper, neodymium, or scandium, or an alloy material containing any of these materials as its main component. Note that the electrode 148a and the conductive layer 148b may have a single-layer structure or a stacked-layer structure.
Then, the insulating layer 150 is formed over the gate insulating layer 146, the electrode 148a, and the conductive layer 148b (see
Next, the insulating layer 152 is formed over the insulating layer 150 (see
Next, an opening reaching the electrode 142a is formed in the gate insulating layer 146, the insulating layer 150, and the insulating layer 152. An electrode 154a is formed in the opening. Then, the wiring 156 in contact with the electrode 154a is formed over the insulating layer 152 (see
The wiring 156 is formed by forming a conductive layer by a PVD method or a CVD method and then by patterning the conductive layer. As a material of the conductive layer, an element selected from aluminum, chromium, copper, tantalum, titanium, molybdenum, and tungsten, an alloy including any of these elements as a component, or the like can be used. A material including one of manganese, magnesium, zirconium, beryllium, neodymium, and scandium or a combination of a plurality of these elements may be used.
Specifically, the electrode 154a can be formed in such a manner that a thin titanium film (about 5 nm) is formed in a region including the opening of the insulating layer 150 and the insulating layer 152 by a PVD method and then an aluminum film is formed so as to be embedded in the opening, for example. Here, the titanium film formed by a PVD method functions to reduce an oxide film (e.g., a natural oxide film) formed on a surface where the titanium film is formed, and to decrease the contact resistance with a lower electrode or the like (here, the electrode 142a). In addition, hillock of the aluminum film can be prevented. A copper film may be formed by a plating method after the formation of a barrier film of titanium, titanium nitride, or the like.
Through the above process, the transistor 162 including the purified oxide semiconductor layer 144 and the capacitor 164 are completed (see
Here, in a structure in which a memory cell is stacked over the memory cell illustrated in
Then, an opening is formed in the insulating layer 140, and the electrode 500 in
The insulating layer 140 can be formed by a PVD method, a CVD method, or the like. The insulating layer 140 can be formed so as to have a single-layer structure or a stacked-layer structure using a material including an inorganic insulating material such as silicon oxide, silicon oxynitride, silicon nitride, hafnium oxide, gallium oxide, or aluminum oxide or a material including an organic material such as polyimide or acrylic.
Note that the electrode 501a and the electrode 501b illustrated in
Note that the electrode 552 illustrated in
Note that in the case of forming the transistor 162 and the capacitor 164 illustrated in
In the case of forming the transistor 162 and the capacitor 164 illustrated in
In the case of forming the transistor 162 and the capacitor 164 illustrated in
In the case of forming the transistor 162 and the capacitor 164 illustrated in
Next, methods for manufacturing the transistors 162 and the capacitors 164 illustrated in
A method for manufacturing the transistor 162 and the capacitor 164 illustrated in
First, the oxide semiconductor layer 144 is formed over the insulating layer 140, and an oxide conductive layer and a conductive layer are stacked over the insulating layer 140 and the oxide semiconductor layer 144.
As a method for forming the oxide conductive layer, a sputtering method, a vacuum evaporation method (an electron beam evaporation method or the like), an arc discharge ion plating method, or a spray method is used. As a material of the oxide conductive layer, zinc oxide, zinc aluminum oxide, zinc aluminum oxynitride, zinc gallium oxide, indium tin oxide, or the like can be used. In addition, any of the above materials may contain silicon oxide. Note that the description of the conductive layer used for forming the electrodes 142a and 142b can be referred to for the film formation method and the material of the conductive layer.
Next, the electrodes 142a and 142b and the oxide conductive layers 143a and 143b are formed by forming a mask over the conductive layer and selectively etching the conductive layer and the oxide conductive layer.
Note that when etching treatment for the conductive layer and the oxide conductive layer is performed, etching conditions (e.g., type of an etching agent, the concentration of an etching agent, and etching time) are adjusted as appropriate in order to prevent excessive etching of the oxide semiconductor layer.
Next, the gate insulating layer 146 is formed over the electrodes 142a and 142b and the oxide semiconductor layer 144. After that, over the gate insulating layer 146, the electrode 148a is formed so as to overlap with the oxide semiconductor layer 144, and the conductive layer 148b is formed so as to overlap with the electrode 142b.
Through the above steps, the transistor 162 and the capacitor 164 are completed (see
In the case of manufacturing the transistor 162 and the capacitor 164 illustrated in
Next, the gate insulating layer 146 is formed over the electrodes 142a and 142b and the oxide semiconductor layer 144. After that, over the gate insulating layer 146, the electrode 148a is formed so as to overlap with the oxide semiconductor layer 144, and the conductive layer 148b is formed so as to overlap with the electrode 142b.
Through the above steps, the transistor 162 and the capacitor 164 are completed (see
In each of the transistors 162 described in this embodiment, the oxide semiconductor layer 144 is purified and thus contains hydrogen at a concentration of 5×1019 atoms/cm3 or less, preferably 5×1018 atoms/cm3 or less, more preferably 5×1017 atoms/cm3 or less. In addition, the carrier density of the oxide semiconductor layer 144 is, for example, less than 1×1012/cm3, preferably less than 1.45×1010/cm3, which is sufficiently lower than the carrier density of a general silicon wafer (approximately 1×1014/cm3). In addition, the off-state current of the transistor 162 is sufficiently small. For example, the off-state current (per unit channel width (1 μm), here) of the transistor 162 at room temperature (25° C.) is 100 zA (1 zA (zeptoampere) is 1×10−21 A) or less, preferably 10 zA or less.
The concentration of an alkali metal or an alkaline earth metal is sufficiently decreased in the oxide semiconductor layer 144. The concentration of an alkali metal or an alkaline earth metal is decreased to such a degree that, for example, the concentrations of Na is 5×1016 cm−3 or less, preferably 1×1016 cm−3 or less, more preferably 1×1015 cm−3 or less, the concentration of Li is 5×1015 cm−3 or less, preferably 1×1015 cm−3 or less, and the concentration of K is 5×1015 cm−3 or less, preferably 1×1015 cm−3 or less.
In this manner, by using the oxide semiconductor layer 144 which is purified and is intrinsic, it becomes easy to sufficiently reduce the off-state current of the transistor 162. With the use of such a transistor 162 as described above, a memory device in which stored data can be held for an extremely long time can be provided.
The configurations, methods, and the like described in this embodiment can be combined as appropriate with any of the configurations, methods, and the like described in the other embodiments.
One embodiment of an oxide semiconductor layer which can be used for a channel formation region of the transistor 162 in the above embodiments will be described with reference to
The oxide semiconductor layer of this embodiment has a stacked structure including a first crystalline oxide semiconductor layer and a second crystalline oxide semiconductor layer which is over the first crystalline oxide semiconductor layer and has a larger thickness than the first crystalline oxide semiconductor layer.
A first oxide semiconductor film with a thickness greater than or equal to 1 nm and less than or equal to 10 nm is formed over an insulating layer 140.
In this embodiment, an oxide insulating layer with a thickness greater than or equal to 50 nm and less than or equal to 600 nm is formed as the insulating layer 140 by a PCVD method or a sputtering method. For example, a single layer selected from a silicon oxide film, a gallium oxide film, an aluminum oxide film, a silicon oxynitride film, an aluminum oxynitride film, and a silicon nitride oxide film or a stack of any of these films can be used.
The first oxide semiconductor film is formed by a sputtering method, and the substrate temperature in the film formation by a sputtering method is set to be higher than or equal to 200° C. and lower than or equal to 400° C. In this embodiment, the first oxide semiconductor film is formed to a thickness of 5 nm in an oxygen atmosphere, an argon atmosphere, or an atmosphere including argon and oxygen under conditions where a target for an oxide semiconductor (a target for an In—Ga—Zn—O-based oxide semiconductor (In2O3:Ga2O3:ZnO=1:1:2 [molar ratio])) is used, the distance between the substrate and the target is 170 mm, the substrate temperature is 250° C., the pressure is 0.4 Pa, and the direct-current (DC) power is 0.5 kW.
Next, first heat treatment is performed under a condition where the atmosphere of a chamber in which the substrate is set is an atmosphere of nitrogen or dry air. The temperature of the first heat treatment is higher than or equal to 400° C. and lower than or equal to 750° C. Through the first heat treatment, a first crystalline oxide semiconductor layer 145a is formed (see
Although it depends on the temperature of the first heat treatment, the first heat treatment causes crystallization from a film surface and crystal grows from the film surface toward the inside of the film; thus, c-axis aligned crystals are obtained. By the first heat treatment, a large amount of zinc and oxygen gather about the film surface, and one or more layers of graphene-type two-dimensional crystal including zinc and oxygen and having a hexagonal upper plane are formed at the outermost surface; the one or more layers at the outermost surface grow in the thickness direction to form a stack of layers. By increasing the temperature of the heat treatment, crystal growth proceeds from the surface to the inside and further from the inside to the bottom.
By the first heat treatment, oxygen in the insulating layer 140 that is an oxide insulating layer is diffused to an interface between the insulating layer 140 and the first crystalline oxide semiconductor layer 145a or the vicinity of the interface (within ±5 nm from the interface), whereby oxygen deficiencies in the first crystalline oxide semiconductor layer are reduced. Therefore, it is preferable that oxygen be included in (a bulk of) the insulating layer 140 used as a base insulating layer for the first crystalline oxide semiconductor layer or at the interface between the first crystalline oxide semiconductor layer 145a and the insulating layer 140 at an amount that exceeds at least the stoichiometric proportion.
Next, a second oxide semiconductor film with a thickness more than 10 nm is formed over the first crystalline oxide semiconductor layer 145a. The second oxide semiconductor film is formed by a sputtering method, and the substrate temperature in the film formation is set to be higher than or equal to 200° C. and lower than or equal to 400° C. By setting the substrate temperature in the film formation to be higher than or equal to 200° C. and lower than or equal to 400° C., precursors can be arranged in the oxide semiconductor film formed above and in contact with the surface of the first crystalline oxide semiconductor layer, and so-called orderliness can be obtained.
In this embodiment, the second oxide semiconductor film is formed to a thickness of 25 nm in an oxygen atmosphere, an argon atmosphere, or an atmosphere including argon and oxygen under conditions where a target for an oxide semiconductor (a target for an In—Ga—Zn—O-based oxide semiconductor (In2O3:Ga2O3:ZnO=1:1:2 [molar ratio])) is used, the distance between the substrate and the target is 170 mm, the substrate temperature is 400° C., the pressure is 0.4 Pa, and the direct-current (DC) power is 0.5 kW.
Next, second heat treatment is performed under a condition where the atmosphere of a chamber in which the substrate is set is an atmosphere of nitrogen or dry air. The temperature of the second heat treatment is higher than or equal to 400° C. and lower than or equal to 750° C. Through the second heat treatment, a second crystalline oxide semiconductor layer 145b is formed (see
It is preferable that steps from the formation of the insulating layer 140 to the second heat treatment be successively performed without exposure to the air. The steps from the formation of the insulating layer 140 to the second heat treatment are preferably performed in an atmosphere which is controlled to include little hydrogen and moisture (such as an inert gas atmosphere, a reduced-pressure atmosphere, or a dry-air atmosphere); in terms of moisture, for example, a dry nitrogen atmosphere with a dew point of −40° C. or lower, preferably a dew point of −50° C. or lower may be employed.
Next, the stack of the oxide semiconductor layers including the first crystalline oxide semiconductor layer 145a and the second crystalline oxide semiconductor layer 145b is processed into an oxide semiconductor layer 145 including a stack of island-shaped oxide semiconductor layers (see
The stack of the oxide semiconductor layers can be processed by being etched after a mask having a desired shape is formed over the stack of the oxide semiconductor layers. The mask may be formed by a method such as photolithography. Alternatively, a method such as an inkjet method may be used to form the mask.
For the etching of the stack of oxide semiconductor layers, either wet etching or dry etching may be employed. It is needless to say that both of them may be employed in combination.
A feature of the first crystalline oxide semiconductor layer and the second crystalline oxide semiconductor layer obtained by the above formation method is that these layers have c-axis alignment. Note that the first crystalline oxide semiconductor layer and the second crystalline oxide semiconductor layer comprise an oxide including a crystal with c-axis alignment (also referred to as c-axis aligned crystal (CAAC)), which has neither a single crystal structure nor an amorphous structure. The first crystalline oxide semiconductor layer and the second crystalline oxide semiconductor layer partly include a crystal grain boundary.
Here, an oxide including crystals with c-axis alignment (also referred to as c-axis aligned crystal (CAAC)), which has a triangular or hexagonal atomic arrangement when seen from the direction of an a-b plane, a surface, or an interface will be described. In the crystal, metal atoms are arranged in a layered manner, or metal atoms and oxygen atoms are arranged in a layered manner along the c-axis, and the direction of the a-axis or the b-axis is varied in the a-b plane (the crystal rotates around the c-axis).
In a broad sense, an oxide including CAAC means a non-single crystal oxide including a phase which has a triangular, hexagonal, regular triangular, or regular hexagonal atomic arrangement when seen from the direction perpendicular to the a-b plane and in which metal atoms are arranged in a layered manner or metal atoms and oxygen atoms are arranged in a layered manner when seen from the direction perpendicular to the c-axis direction.
The CAAC is not a single crystal, but this does not mean that the CAAC is composed of only an amorphous component. Although the CAAC includes a crystallized portion (crystalline portion), a boundary between one crystalline portion and another crystalline portion is not clear in some cases.
In the case where oxygen is included in the CAAC, nitrogen may be substituted for part of oxygen included in the CAAC. The c-axes of individual crystalline portions included in the CAAC may be aligned in one direction (e.g., a direction perpendicular to a surface of a substrate over which the CAAC is formed or a surface of the CAAC). Alternatively, the normals of the a-b planes of the individual crystalline portions included in the CAAC may be aligned in one direction (e.g., a direction perpendicular to a surface of a substrate over which the CAAC is formed or a surface of the CAAC).
The CAAC becomes a conductor, a semiconductor, or an insulator depending on its composition or the like. The CAAC transmits or does not transmit visible light depending on its composition or the like.
As an example of such a CAAC, there is a crystal which is formed into a film shape and has a triangular or hexagonal atomic arrangement when observed from the direction perpendicular to a surface of the film or a surface of a supporting substrate, and in which metal atoms are arranged in a layered manner or metal atoms and oxygen atoms (or nitrogen atoms) are arranged in a layered manner when a cross section of the film is observed.
An example of a crystal structure of the CAAC will be described in detail with reference to
Here, a plurality of small groups forms a medium group, and a plurality of medium groups forms a large group (also referred to as a unit cell).
Now, a rule of bonding between the small groups will be described. The three O atoms in the upper half with respect to the hexacoordinate In atom in
A metal atom whose coordination number is 4, 5, or 6 is bonded to another metal atom through a tetracoordinate O atom in the c-axis direction. In addition to the above, a medium group can be formed in a different manner by combining a plurality of small groups so that the total electric charge of the layered structure is 0.
In
In the medium group included in the layered structure of the In—Sn—Zn—O-based material in
Here, electric charge for one bond of a tricoordinate O atom and electric charge for one bond of a tetracoordinate O atom can be assumed to be −0.667 and −0.5, respectively. For example, electric charge of a (hexacoordinate or pentacoordinate) In atom, electric charge of a (tetracoordinate) Zn atom, and electric charge of a (pentacoordinate or hexacoordinate) Sn atom are +3, +2, and +4, respectively. Accordingly, electric charge in a small group including a Sn atom is +1. Therefore, electric charge of −1, which cancels +1, is needed to form a layered structure including a Sn atom. As a structure having electric charge of −1, the small group including two Zn atoms as illustrated in
When the large group illustrated in
The above-described rule also applies to the following oxides: a four-component metal oxide such as an In—Sn—Ga—Zn-based oxide; a three-component metal oxide such as an In—Ga—Zn-based oxide (also referred to as IGZO), an In—Al—Zn-based oxide, a Sn—Ga—Zn-based oxide, an Al—Ga—Zn-based oxide, a Sn—Al—Zn-based oxide, an In—Hf—Zn-based oxide, an In—La—Zn-based oxide, an In—Ce—Zn-based oxide, an In—Pr—Zn-based oxide, an In—Nd—Zn-based oxide, an In—Sm—Zn-based oxide, an In—Eu—Zn-based oxide, an In—Gd—Zn-based oxide, an In—Tb—Zn-based oxide, an In—Dy—Zn-based oxide, an In—Ho—Zn-based oxide, an In—Er—Zn-based oxide, an In—Tm—Zn-based oxide, an In—Yb—Zn-based oxide, or an In—Lu—Zn-based oxide; a two-component metal oxide such as an In—Zn-based oxide, a Sn—Zn-based oxide, an Al—Zn-based oxide, a Zn—Mg-based oxide, a Sn—Mg-based oxide, an In—Mg-based oxide, or an In—Ga-based oxide; and the like.
As an example,
In the medium group included in the layered structure of the In—Ga—Zn—O-based material in
Here, since electric charge of a (hexacoordinate or pentacoordinate) In atom, electric charge of a (tetracoordinate) Zn atom, and electric charge of a (pentacoordinate) Ga atom are +3, +2, and +3, respectively, electric charge of a small group including any of an In atom, a Zn atom, and a Ga atom is 0. As a result, the total electric charge of a medium group having a combination of such small groups is always 0.
In order to form the layered structure of the In—Ga—Zn—O-based material, a large group can be formed using not only the medium group illustrated in
In any case, in order to obtain CAAC, it is important to form hexagonal crystals in an initial stage of deposition of an oxide semiconductor film and to cause crystal growth from the hexagonal crystals as a seed. In order to achieve this, it is preferable that a substrate heating temperature be 100° C. to 500° C., more preferably 200° C. to 400° C., still preferably 250° C. to 300° C. In addition, the deposited oxide semiconductor film is subjected to heat treatment at a temperature higher than the substrate heating temperature in the film formation. Accordingly, microdefects in the film and defects at the interface of stacked layers can be repaired.
Note that the first and second crystalline oxide semiconductor layers are formed using an oxide material containing at least Zn, for example, a four-component metal oxide such as an In—Al—Ga—Zn—O-based material, or an In—Sn—Ga—Zn—O-based material; a three-component metal oxide such as an In—Ga—Zn—O-based material, an In—Al—Zn—O-based material, an In—Sn—Zn—O-based material, a Sn—Ga—Zn—O-based material, an Al—Ga—Zn—O-based material, or a Sn—Al—Zn—O-based material; a two-component metal oxide such as an In—Zn—O-based material, a Sn—Zn—O-based material, an Al—Zn—O-based material, or a Zn—Mg—O-based material; or a Zn—O-based material. In addition, an In—Si—Ga—Zn—O-based material, an In—Ga—B—Zn—O-based material, or an In—B—Zn—O-based material may be used. In addition, the above materials may contain SiO2. Here, for example, an In—Ga—Zn—O-based material means an oxide material containing indium (In), gallium (Ga), and zinc (Zn), and there is no limitation on the composition ratio thereof. Further, the In—Ga—Zn—O-based material may include an element other than In, Ga, and Zn.
Without limitation to the two-layer structure in which the second crystalline oxide semiconductor layer is formed over the first crystalline oxide semiconductor layer, a stacked structure including three or more layers may be formed by repeatedly performing a process of film formation and heat treatment for forming a third crystalline oxide semiconductor layer after the second crystalline oxide semiconductor layer is formed.
After that, the electrodes 142a and 142b, the gate insulating layer 146, the electrode 148a, and the conductive layer 148b are formed; thus, the transistor 162 and the capacitor 164 are completed (see
The oxide semiconductor layer 145 including the stack of the oxide semiconductor layers formed by the above formation method can be used as appropriate for the transistor 162 described in Embodiment 2.
In the transistor 162, in which the stack of the oxide semiconductor layers of this embodiment is used as the oxide semiconductor layer 144, an electric field is not applied from one surface to the other surface of the oxide semiconductor layer and current does not flow in the thickness direction of the stack of the oxide semiconductor layers. The transistor has a structure in which current mainly flows along the interface of the stack of the oxide semiconductor layers; therefore, even when the transistor 162 is irradiated with light or even when a BT stress is applied to the transistor 162, deterioration of transistor characteristics is suppressed or reduced.
By forming the transistor 162 with the use of a stack of a first crystalline oxide semiconductor layer and a second crystalline oxide semiconductor layer, like the oxide semiconductor layer 145, the transistor can have stable electrical characteristics and high reliability.
This embodiment can be implemented in an appropriate combination with the structures described in the other embodiments.
In this embodiment, application of the memory device described in any of the above embodiments to a semiconductor device such as an electronic device will be described with reference to
As described above, the memory device in any of the above embodiments is mounted on each of the electronic devices described in this embodiment. Therefore, electronic devices in which power consumption is reduced can be realized.
The actually measured field-effect mobility of an insulated gate transistor can be lower than its intrinsic mobility because of a variety of reasons; this phenomenon occurs not only in the case of using an oxide semiconductor. One of the reasons that reduce the mobility is a defect inside a semiconductor or a defect at an interface between the semiconductor and an insulating film. When a Levinson model is used, the field-effect mobility on the assumption that no defect exists inside the semiconductor can be calculated theoretically. In this embodiment, the field-effect mobility of an ideal oxide semiconductor without a defect inside the semiconductor is calculated theoretically, and calculation results of characteristics of minute transistors that are manufactured using such an oxide semiconductor are shown.
Assuming that the intrinsic mobility and the measured field-effect mobility of a semiconductor are μ0 and μ, respectively, and a potential barrier (such as a grain boundary) exists in the semiconductor, the measured field-effect mobility can be expressed as the following formula.
Here, E represents the height of the potential barrier, k represents the Boltzmann constant, and T represents the absolute temperature. When the potential barrier is assumed to be attributed to a defect, the height of the potential barrier can be expressed as the following formula according to the Levinson model.
Here, e represents the elementary charge, N represents the average defect density per unit area in a channel, ∈ represents the dielectric constant of the semiconductor, n represents the number of carriers per unit area in the channel, Cox represents the capacitance per unit area Vg represents the gate voltage, and t represents the thickness of the channel. In the case where the thickness of the semiconductor layer is less than or equal to 30 nm, the thickness of the channel may be regarded as being the same as the thickness of the semiconductor layer. The drain current Id in a linear region can be expressed as the following formula.
Here, L represents the channel length and W represents the channel width, and L and W are each 10 μm. In addition, Vd represents the drain voltage. When dividing both sides of the above equation by Vg and then taking logarithms of both sides, the following formula can be obtained.
The right side of Formula 5 is a function of Vg. From the formula, it is found that the defect density N can be obtained from the slope of a line in a graph which is obtained by plotting actual measured values with ln(Id/Vg) as the ordinate and 1/Vg as the abscissa. That is, the defect density can be evaluated from the Id−Vg characteristics of the transistor. The defect density N of an oxide semiconductor in which the ratio of indium (In), tin (Sn), and zinc (Zn) is 1:1:1 is approximately 1×1012/cm2.
On the basis of the defect density obtained in this manner, or the like, μ0 can be calculated to be 120 cm2/Vs from Formula 2 and Formula 3. The measured mobility of an In—Sn—Zn oxide including a defect is approximately 35 cm2/Vs. However, assuming that no defect exists inside the semiconductor and at the interface between the semiconductor and an insulating film, the mobility μ0 of the oxide semiconductor is expected to be 120 cm2/Vs.
Note that even when no defect exists inside a semiconductor, scattering at an interface between a channel and a gate insulating layer affects the transport property of the transistor. In other words, the mobility μ1 at a position that is distance x away from the interface between the channel and the gate insulating layer can be expressed as the following formula.
Here, D represents the electric field in the gate direction, and B and G are constants. B and G can be obtained from actual measurement results; according to the above measurement results, B is 4.75×107 cm/s and G is 10 nm (the depth to which the influence of interface scattering reaches). When D is increased (i.e., when the gate voltage is increased), the second term of Formula 6 is increased and accordingly the mobility μ is decreased.
Calculation results of the mobility μ2 of a transistor whose channel includes an ideal oxide semiconductor without a defect inside the semiconductor are shown in
Further, the work functions of a gate, a source, and a drain were assumed to be 5.5 eV, 4.6 eV, and 4.6 eV, respectively. The thickness of a gate insulating layer was assumed to be 100 nm, and the relative permittivity thereof was assumed to be 4.1. The channel length and the channel width were each assumed to be 10 μm, and the drain voltage Vd was assumed to be 0.1 V.
As shown in
Calculation results of characteristics of minute transistors which are manufactured using an oxide semiconductor having such a mobility are shown in
The transistor illustrated in
A gate insulating layer 8104 is formed between the gate 8105 and the semiconductor region 8103b. In addition, a sidewall insulator 8106a and a sidewall insulator 8106b are formed on both side surfaces of the gate 8105, and an insulator 8107 is formed over the gate 8105 so as to prevent a short circuit between the gate 8105 and another wiring. The sidewall insulator has a width of 5 nm. A source 8108a and a drain 8108b are provided in contact with the semiconductor region 8103a and the semiconductor region 8103c, respectively. Note that the channel width of this transistor is 40 nm.
The transistor of
The transistor illustrated in
The other parameters used in calculation are as described above. For the calculation, device simulation software Sentaurus Device manufactured by Synopsys, Inc. was used.
Further,
In either of the structures, as the gate insulating layer is thinner, the off-state current is significantly decreased, whereas no noticeable change arises in the peak value of the mobility μ and the on-state current.
Note that the peak of the mobility μ is approximately 80 cm2/Vs in
This embodiment can be implemented by being combined as appropriate with any of the above-described embodiments.
A transistor in which an oxide semiconductor containing In, Sn, and Zn as main components is used as a channel formation region can have favorable characteristics by depositing the oxide semiconductor while heating a substrate or by performing heat treatment after an oxide semiconductor film is formed. Note that a main component refers to an element included in a composition at greater than or equal to 5 atomic %. In this embodiment, the case where the field effect mobility of the transistor is improved by intentionally heating the substrate after formation of the oxide semiconductor film will be described with reference to
By intentionally heating the substrate after formation of the oxide semiconductor film including In, Sn, and Zn as main components, the field-effect mobility of the transistor can be improved. Further, the threshold voltage of the transistor can be positively shifted to make the transistor normally off.
As an example,
The field-effect mobility can be further improved by performing heat treatment after formation of the oxide semiconductor film including In, Sn, and Zn as main components.
The intentional heating of the substrate is expected to have an effect of reducing moisture taken into the oxide semiconductor film during the formation by sputtering. Further, the heat treatment after film formation enables hydrogen, a hydroxyl group, or moisture to be released and removed from the oxide semiconductor film. In this manner, the field-effect mobility can be improved. Such an improvement in field-effect mobility is presumed to be achieved not only by removal of impurities by dehydration or dehydrogenation but also by a reduction in interatomic distance due to an increase in density. The oxide semiconductor can be crystallized by being purified by removal of impurities from the oxide semiconductor. In the case of using such a purified non-single crystal oxide semiconductor, ideally, a field-effect mobility exceeding 100 cm2/Vsec is expected to be realized.
The oxide semiconductor including In, Sn, and Zn as main components may be crystallized in the following manner: oxygen ions are implanted into the oxide semiconductor, hydrogen, a hydroxyl group, or moisture included in the oxide semiconductor is released by heat treatment, and the oxide semiconductor is crystallized through the heat treatment or by another heat treatment performed later. By such crystallization treatment or recrystallization treatment, a non-single-crystal oxide semiconductor having favorable crystallinity can be obtained.
The intentional heating of the substrate during film formation and/or the heat treatment after the film formation contributes not only to improving field-effect mobility but also to making the transistor normally off. In a transistor in which an oxide semiconductor film that includes In, Sn, and Zn as main components and is formed without heating a substrate intentionally is used as a channel formation region, the threshold voltage tends to be shifted negatively. However, when the oxide semiconductor film formed while heating the substrate intentionally is used, the problem of the negative shift of the threshold voltage can be solved. That is, the threshold voltage is shifted so that the transistor becomes normally off; this tendency can be confirmed by comparison between
Note that the threshold voltage can also be controlled by changing the ratio of In, Sn, and Zn; when the composition ratio of In, Sn, and Zn is 2:1:3, a normally-off transistor is expected to be formed. In addition, an oxide semiconductor film having high crystallinity can be obtained by setting the composition ratio of a target as follows: In:Sn:Zn=2:1:3.
The temperature of the intentional heating of the substrate or the temperature of the heat treatment is 150° C. or higher, preferably 200° C. or higher, further preferably 400° C. or higher. When film formation or heat treatment is performed at a high temperature, the transistor can be normally off.
By intentionally heating the substrate during film formation and/or by performing heat treatment after the film formation, the stability against a gate-bias stress can be increased. For example, when a gate bias is applied under a condition of 2 MV/cm at 150° C. for one hour, drift of the threshold voltage can be less than ±1.5 V, preferably less than ±1.0 V.
A BT test was performed on the following two transistors: Sample 1 on which heat treatment was not performed after formation of an oxide semiconductor film, and Sample 2 on which heat treatment at 650° C. was performed after formation of an oxide semiconductor film.
First, Vg−Id characteristics of the transistors were measured at a substrate temperature of 25° C. and Vds of 10 V. Note that Vds refers to a drain voltage (a potential difference between a drain and a source). Then, the substrate temperature was set to 150° C. and Vds was set to 0.1 V. After that, 20 V of Vg was applied so that an electric field intensity applied to gate insulating films was 2 MV/cm, and the condition was kept for one hour. Next, Vg was set to 0 V. Then, Vg−Id characteristics of the transistors were measured at a substrate temperature of 25° C. and Vds of 10 V. This process is called a positive BT test.
In a similar manner, first, Vg−Id characteristics of the transistors were measured at a substrate temperature of 25° C. and Vds of 10 V. Then, the substrate temperature was set at 150° C. and Vds was set to 0.1 V. After that, −20 V of Vg was applied so that an electric field intensity applied to the gate insulating films was −2 MV/cm, and the condition was kept for one hour. Next, Vg was set to 0 V. Then, Vg−Id characteristics of the transistors were measured at a substrate temperature of 25° C. and Vds of 10 V. This process is called a negative BT test.
The amount of shift in the threshold voltage of Sample 1 due to the positive BT test and that due to the negative BT test were 1.80 V and −0.42 V, respectively. The amount of shift in the threshold voltage of Sample 2 due to the positive BT test and that due to the negative BT test were 0.79 V and 0.76 V, respectively. It is found that, in each of Sample 1 and Sample 2, the amount of shift in the threshold voltage between before and after the BT tests is small and the reliability is high.
The heat treatment can be performed in an oxygen atmosphere; alternatively, the heat treatment may be performed first in an atmosphere of nitrogen or an inert gas or under reduced pressure, and then in an atmosphere including oxygen. Oxygen is supplied to the oxide semiconductor after dehydration or dehydrogenation, whereby an effect of the heat treatment can be further increased. As a method for supplying oxygen after dehydration or dehydrogenation, a method in which oxygen ions are accelerated by an electric field and implanted into the oxide semiconductor film may be employed.
A defect due to oxygen deficiency is easily caused in the oxide semiconductor or at an interface between the oxide semiconductor and a film in contact with the oxide semiconductor; however, when excess oxygen is included in the oxide semiconductor by the heat treatment, oxygen deficiency caused constantly can be compensated for with excess oxygen. The excess oxygen is oxygen existing mainly between lattices. When the concentration of excess oxygen is set to higher than or equal to 1×1016/cm3 and lower than or equal to 2×1020/cm3, excess oxygen can be included in the oxide semiconductor without causing crystal distortion or the like.
When heat treatment is performed so that at least part of the oxide semiconductor includes crystal, a more stable oxide semiconductor film can be obtained. For example, when an oxide semiconductor film which is formed by sputtering using a target having a composition ratio of In:Sn:Zn=1:1:1 without heating a substrate intentionally is analyzed by X-ray diffraction (XRD), a halo pattern is observed. The formed oxide semiconductor film can be crystallized by being subjected to heat treatment. The temperature of the heat treatment can be set as appropriate; when the heat treatment is performed at 650° C., for example, a clear diffraction peak can be observed in an X-ray diffraction analysis.
An XRD analysis of an In—Sn—Zn—O film was conducted. The XRD analysis was conducted using an X-ray diffractometer D8 ADVANCE manufactured by Bruker AXS, and measurement was performed by an out-of-plane method.
Sample A and Sample B were prepared and the XRD analysis was performed thereon. A method for manufacturing Sample A and Sample B will be described below.
An In—Sn—Zn—O film with a thickness of 100 nm was formed over a quartz substrate that had been subjected to dehydrogenation treatment.
The In—Sn—Zn—P film was formed with a sputtering apparatus with a power of 100 W (DC) in an oxygen atmosphere. An In—Sn—Zn—O target having an atomic ratio of In:Sn:Zn=1:1:1 was used as a target. Note that the substrate heating temperature in film formation was set at 200° C. A sample manufactured in this manner was used as Sample A.
Next, a sample manufactured by a method similar to that of Sample A was subjected to heat treatment at 650° C. As the heat treatment, heat treatment in a nitrogen atmosphere was first performed for one hour and heat treatment in an oxygen atmosphere was further performed for one hour without lowering the temperature. A sample manufactured in this manner was used as Sample B.
These substrate heating and heat treatment have an effect of preventing hydrogen and a hydroxyl group, which are unfavorable impurities for an oxide semiconductor, from being included in the film or an effect of removing hydrogen and a hydroxyl group from the film. That is, an oxide semiconductor can be purified by removing hydrogen serving as a donor impurity from the oxide semiconductor, whereby a normally-off transistor can be obtained. The purification of an oxide semiconductor enables the off-state current of the transistor to be 1 aA/μm or lower. Here, the unit of the off-state current is used to indicate current per micrometer of a channel width.
Specifically, as shown in
Note that in order to prevent hydrogen and moisture from being included in the oxide semiconductor film during formation thereof, it is preferable to increase the purity of a sputtering gas by sufficiently suppressing leakage from the outside of a deposition chamber and degasification through an inner wall of the deposition chamber. For example, a gas with a dew point of −70° C. or lower is preferably used as the sputtering gas in order to prevent moisture from being included in the film. In addition, it is preferable to use a target which is purified so as not to include impurities such as hydrogen and moisture. Although it is possible to remove moisture from a film of an oxide semiconductor including In, Sn, and Zn as main components by heat treatment, a film which does not include moisture originally is preferably formed because moisture is released from the oxide semiconductor including In, Sn, and Zn as main components at a higher temperature than from an oxide semiconductor including In, Ga, and Zn as main components.
The relation between the substrate temperature and electrical characteristics of a transistor formed using Sample B, on which heat treatment at 650° C. was performed after formation of the oxide semiconductor film, was evaluated.
The transistor used for the measurement has a channel length L of 3 μm, a channel width W of 10 μm, Lov of 0 μm, and dW of 0 μm. Note that Vds was set to 10 V. Note that the substrate temperature was −40° C., −25° C., 25° C., 75° C., 125° C., and 150° C. Here, in a transistor, the width of a portion where a gate electrode overlaps with one of a pair of electrodes is referred to as Lov, and the width of a portion of the pair of electrodes, which does not overlap with an oxide semiconductor film, is referred to as dW.
From
From
In a transistor in which such an oxide semiconductor including In, Sn, and Zn as main components is used as a channel formation region, a field-effect mobility of 30 cm2/Vsec or higher, preferably 40 cm2/Vsec or higher, further preferably 60 cm2/Vsec or higher can be obtained with the off-state current maintained at 1 aA/μm or lower, which can achieve on-state current needed for an LSI. For example, in an FET where L/W is 33 nm/40 nm, an on-state current of 12 μA or higher can flow when the gate voltage is 2.7 V and the drain voltage is 1.0 V. In addition, sufficient electrical characteristics can be ensured in a temperature range needed for operation of a transistor.
With such characteristics, an integrated circuit having a novel function can be realized without decreasing the operation speed even when a transistor including an oxide semiconductor is also provided in an integrated circuit formed using a Si semiconductor.
As described above, by intentionally heating a substrate during deposition of an oxide semiconductor including In, Sn, and Zn as main components and/or by performing heat treatment after the deposition, characteristics of a transistor can be improved.
This embodiment can be implemented by being combined as appropriate with any of the above embodiments.
In this example, an example of a transistor in which an In—Sn—Zn—O film is used as an oxide semiconductor film will be described with reference to
The transistor illustrated in
Although not illustrated, a protective film may be provided to cover the interlayer insulating film 1116 and the wiring 1118. With the protective film, a minute amount of leakage current generated by surface conduction of the interlayer insulating film 1116 can be reduced and thus the off-state current of the transistor can be reduced.
This example can be implemented by being combined as appropriate with any of the above embodiments.
In this example, another example of a transistor in which an In—Sn—Zn—O film is used as an oxide semiconductor film will be described.
The transistor illustrated in
As the substrate 600, a glass substrate can be used. As the base insulating layer 602, a silicon oxide film can be used. As the oxide semiconductor film 606, an In—Sn—Zn—O film can be used. As the pair of electrodes 614, a tungsten film can be used. As the gate insulating film 608, a silicon oxide film can be used. The gate electrode 610 can have a stacked structure of a tantalum nitride film and a tungsten film. The interlayer insulating film 616 can have a stacked structure of a silicon oxynitride film and a polyimide film. The wirings 618 can each have a stacked structure in which a titanium film, an aluminum film, and a titanium film are formed in this order. As the protective film 620, a polyimide film can be used.
Note that in the transistor having the structure illustrated in
This example can be implemented by being combined as appropriate with any of the above embodiments and example.
100: substrate, 106: element separation insulating layer, 108: gate insulating layer, 110: gate electrode, 116: channel formation region, 120: impurity region, 124: metal compound region, 126: electrode, 128: insulating layer, 140: insulating layer, 144: oxide semiconductor layer, 145: oxide semiconductor layer, 146: gate insulating layer, 148: electrode layer, 150: insulating layer, 151: insulating layer, 152: insulating layer, 156: wiring, 159: conductive layer, 160: transistor, 162: transistor, 164: capacitor, 170: memory cell, 201: memory cell array, 210: peripheral circuit, 211: driver circuit, 212: driver circuit, 213: driver circuit, 214: driver circuit, 215: driver circuit, 218: controller, 219: mode register, 220: I/O buffer, 221: address buffer, 222: sense amplifier, 250: center point, 401: transistor, 402: transistor, 403: transistor, 404: transistor, 405: transistor, 406: transistor, 407: transistor, 408: transistor, 409: transistor, 410: transistor, 411: transistor, 500: electrode, 551: electrode, 552: electrode, 553: electrode, 556: electrode, 557: electrode, 601: memory cell array, 611: bit line driver circuit, 612: word line driver circuit, 600: substrate, 602: base insulating layer, 604: one pair of electrodes, 606: oxide semiconductor film, 608: gate insulating film, 610: gate electrode, 614: one pair of electrodes, 616: interlayer insulating film, 618: wiring, 620: protective film, 701: housing, 702: housing, 703: display portion, 704: keyboard, 711L main body, 712: stylus, 713: display portion, 714: operation button, 715: external interface, 720: e-book reader, 721: housing, 723: housing, 725: display portion, 727: display portion, 731: power switch, 733: operation key, 735: speaker, 737: hinge portion, 740: housing, 741: housing, 742: display panel, 743: speaker, 744: microphone, 745: operation key, 746: pointing device, 747: camera lens, 748: external connection terminal, 749: solar cell, 750: external memory slot, 761: main body, 763: eyepiece, 764: operation switch, 765: display portion, 766: battery, 767: display portion, 770: television device, 771: housing, 773: display portion, 775: stand, 780: remote controller, 840: electrode, 841: electrode, 842: insulating layer, 130a: drain electrode, 130b: drain electrode, 136a: electrode, 136b: electrode, 136c: electrode, 142a: electrode, 142b: electrode, 143a: oxide conductive layer, 143b: oxide conductive layer, 145a: crystalline oxide semiconductor layer, 145b: crystalline oxide semiconductor layer, 148a: electrode, 148b: conductive layer, 154a: electrode, 170a: memory cell, 170b: memory cell, 170c: memory cell, 170d: memory cell, 201a: memory cell array, 201b: memory cell array, 211a: driver circuit, 211b: driver circuit, 212a: driver circuit, 212b: driver circuit, 213a: driver circuit, 213b: driver circuit, 214a: driver circuit, 214b: driver circuit, 216a: sense amplifier group, 216b: sense amplifier group, 217a: column decoder, 217b: column decoder, 223a: row decoder, 223b: row decoder, 501a: electrode, 501b: electrode, 502a: electrode, 502b: electrode, 601A: memory cell array, 601B: memory cell array, 601C: memory cell array, 601D: memory cell array, 1101: substrate, 1102: base insulating layer, 1104: protective insulating film, 1106a: high-resistance region, 1106b: low-resistance region, 1106: oxide semiconductor film, 1108: gate insulating film, 1110: gate electrode, 1112: sidewall insulating film, 1114: one pair of electrodes, 1116: interlayer insulating film, 1118: wiring, 8101: base insulating layer, 8102: embedded insulator, 8103a: semiconductor region, 8103b: semiconductor region, 8103c: semiconductor region, 8104: gate insulating layer, 8105: gate, 8106a: sidewall insulator, 8106b: sidewall insulator, 8107: insulator, 8108a: source, and 8108b: drain.
This application is based on Japanese Patent Application serial no. 2010-204090 filed with Japan Patent Office on Sep. 13, 2010, and Japanese Patent Application serial no. 2011-108899 filed with Japan Patent Office on May 14, 2011, the entire contents of which are hereby incorporated by reference.
Number | Date | Country | Kind |
---|---|---|---|
2010-204090 | Sep 2010 | JP | national |
2011-108899 | May 2011 | JP | national |
Number | Name | Date | Kind |
---|---|---|---|
4466081 | Masuoka | Aug 1984 | A |
5060191 | Nagasaki et al. | Oct 1991 | A |
5349366 | Yamazaki et al. | Sep 1994 | A |
5375085 | Gnade et al. | Dec 1994 | A |
5487031 | Gnade et al. | Jan 1996 | A |
5731856 | Kim et al. | Mar 1998 | A |
5744864 | Cillessen et al. | Apr 1998 | A |
6127702 | Yamazaki et al. | Oct 2000 | A |
6294274 | Kawazoe et al. | Sep 2001 | B1 |
6445026 | Kubota et al. | Sep 2002 | B1 |
6563174 | Kawasaki et al. | May 2003 | B2 |
6690598 | Oguchi et al. | Feb 2004 | B2 |
6727522 | Kawasaki et al. | Apr 2004 | B1 |
6765844 | Fujisawa et al. | Jul 2004 | B2 |
6791863 | Oguchi et al. | Sep 2004 | B2 |
6846703 | Shimoda et al. | Jan 2005 | B2 |
6881975 | Anzai et al. | Apr 2005 | B2 |
6972985 | Rinerson et al. | Dec 2005 | B2 |
7026647 | Wu et al. | Apr 2006 | B2 |
7049190 | Takeda et al. | May 2006 | B2 |
7061014 | Hosono et al. | Jun 2006 | B2 |
7064346 | Kawasaki et al. | Jun 2006 | B2 |
7105868 | Nause et al. | Sep 2006 | B2 |
7189992 | Wager, III et al. | Mar 2007 | B2 |
7211825 | Shih et al | May 2007 | B2 |
7282782 | Hoffman et al. | Oct 2007 | B2 |
7297977 | Hoffman et al. | Nov 2007 | B2 |
7323356 | Hosono et al. | Jan 2008 | B2 |
7339187 | Wager, III et al. | Mar 2008 | B2 |
7385224 | Ishii et al. | Jun 2008 | B2 |
7402506 | Levy et al. | Jul 2008 | B2 |
7411209 | Endo et al. | Aug 2008 | B2 |
7453065 | Saito et al. | Nov 2008 | B2 |
7453087 | Iwasaki | Nov 2008 | B2 |
7462862 | Hoffman et al. | Dec 2008 | B2 |
7468304 | Kaji et al. | Dec 2008 | B2 |
7501293 | Ito et al. | Mar 2009 | B2 |
7554169 | Anzai et al. | Jun 2009 | B2 |
7663174 | Shibata | Feb 2010 | B2 |
7674650 | Akimoto et al. | Mar 2010 | B2 |
7696063 | Tsuchiya | Apr 2010 | B2 |
7732819 | Akimoto et al. | Jun 2010 | B2 |
7791074 | Iwasaki | Sep 2010 | B2 |
7888207 | Wager, III et al. | Feb 2011 | B2 |
7910490 | Akimoto et al. | Mar 2011 | B2 |
7932521 | Akimoto et al. | Apr 2011 | B2 |
7939831 | Anzai et al. | May 2011 | B2 |
8008137 | Wu et al. | Aug 2011 | B2 |
8036010 | Maejima | Oct 2011 | B2 |
8179707 | Song et al. | May 2012 | B2 |
8202365 | Umeda et al. | Jun 2012 | B2 |
8274077 | Akimoto et al. | Sep 2012 | B2 |
8314032 | Kawamura et al. | Nov 2012 | B2 |
8378341 | Hayashi et al. | Feb 2013 | B2 |
8378403 | Kato | Feb 2013 | B2 |
8482001 | Yamazaki et al. | Jul 2013 | B2 |
8508967 | Yamazaki et al. | Aug 2013 | B2 |
8610187 | Yamazaki et al. | Dec 2013 | B2 |
8637865 | Kato | Jan 2014 | B2 |
20010015450 | Sugibayashi et al. | Aug 2001 | A1 |
20010046027 | Tai et al. | Nov 2001 | A1 |
20020018357 | Oguchi et al. | Feb 2002 | A1 |
20020056838 | Ogawa | May 2002 | A1 |
20020132454 | Ohtsu et al. | Sep 2002 | A1 |
20030057423 | Shimoda et al. | Mar 2003 | A1 |
20030189401 | Kido et al. | Oct 2003 | A1 |
20030202404 | Scheuerlein | Oct 2003 | A1 |
20030218221 | Wager, III et al. | Nov 2003 | A1 |
20030218222 | Wager et al. | Nov 2003 | A1 |
20040038446 | Takeda et al. | Feb 2004 | A1 |
20040127038 | Carcia et al. | Jul 2004 | A1 |
20040245555 | Ueda | Dec 2004 | A1 |
20040251461 | Anzai et al. | Dec 2004 | A1 |
20050017302 | Hoffman | Jan 2005 | A1 |
20050199959 | Chiang et al. | Sep 2005 | A1 |
20050243595 | Rinerson et al. | Nov 2005 | A1 |
20050280000 | Ishii et al. | Dec 2005 | A1 |
20060035452 | Carcia et al. | Feb 2006 | A1 |
20060043377 | Hoffman et al. | Mar 2006 | A1 |
20060091793 | Baude et al. | May 2006 | A1 |
20060108529 | Saito et al. | May 2006 | A1 |
20060108636 | Sano et al. | May 2006 | A1 |
20060110867 | Yabuta et al. | May 2006 | A1 |
20060113536 | Kumomi et al. | Jun 2006 | A1 |
20060113539 | Sano et al. | Jun 2006 | A1 |
20060113549 | Den et al. | Jun 2006 | A1 |
20060113565 | Abe et al. | Jun 2006 | A1 |
20060169973 | Isa et al. | Aug 2006 | A1 |
20060170111 | Isa et al. | Aug 2006 | A1 |
20060197092 | Hoffman et al. | Sep 2006 | A1 |
20060208977 | Kimura | Sep 2006 | A1 |
20060216877 | Toyota et al. | Sep 2006 | A1 |
20060228974 | Thelss et al. | Oct 2006 | A1 |
20060231882 | Kim et al. | Oct 2006 | A1 |
20060238135 | Kimura | Oct 2006 | A1 |
20060244107 | Sugihara | Nov 2006 | A1 |
20060284171 | Levy et al. | Dec 2006 | A1 |
20060284172 | Ishii | Dec 2006 | A1 |
20060292777 | Dunbar | Dec 2006 | A1 |
20070024187 | Shin et al. | Feb 2007 | A1 |
20070046191 | Saito | Mar 2007 | A1 |
20070052025 | Yabuta | Mar 2007 | A1 |
20070054507 | Kaji et al. | Mar 2007 | A1 |
20070090365 | Hayashi et al. | Apr 2007 | A1 |
20070108446 | Akimoto | May 2007 | A1 |
20070128815 | Iino et al. | Jun 2007 | A1 |
20070141784 | Wager et al. | Jun 2007 | A1 |
20070152217 | Lai et al. | Jul 2007 | A1 |
20070172591 | Seo et al. | Jul 2007 | A1 |
20070187678 | Hirao et al. | Aug 2007 | A1 |
20070187760 | Furuta et al. | Aug 2007 | A1 |
20070194379 | Hosono et al. | Aug 2007 | A1 |
20070215906 | Wu et al. | Sep 2007 | A1 |
20070252928 | Ito et al. | Nov 2007 | A1 |
20070263423 | Scheuerlein et al. | Nov 2007 | A1 |
20070272922 | Kim et al. | Nov 2007 | A1 |
20070287296 | Chang | Dec 2007 | A1 |
20080006877 | Mardilovich et al. | Jan 2008 | A1 |
20080038882 | Takechi et al. | Feb 2008 | A1 |
20080038929 | Chang | Feb 2008 | A1 |
20080050595 | Nakagawara et al. | Feb 2008 | A1 |
20080073653 | Iwasaki | Mar 2008 | A1 |
20080083950 | Pan et al. | Apr 2008 | A1 |
20080106191 | Kawase | May 2008 | A1 |
20080108198 | Wager, III et al. | May 2008 | A1 |
20080128689 | Lee et al. | Jun 2008 | A1 |
20080129195 | Ishizaki et al. | Jun 2008 | A1 |
20080166834 | Kim et al. | Jul 2008 | A1 |
20080182358 | Cowdery-Corvan et al. | Jul 2008 | A1 |
20080224133 | Park et al. | Sep 2008 | A1 |
20080254569 | Hoffman et al. | Oct 2008 | A1 |
20080258139 | Ito et al. | Oct 2008 | A1 |
20080258140 | Lee et al. | Oct 2008 | A1 |
20080258141 | Park et al. | Oct 2008 | A1 |
20080258143 | Kim et al. | Oct 2008 | A1 |
20080296568 | Ryu et al. | Dec 2008 | A1 |
20080308796 | Akimoto et al. | Dec 2008 | A1 |
20080308805 | Akimoto et al. | Dec 2008 | A1 |
20080308806 | Akimoto et al. | Dec 2008 | A1 |
20080315193 | Kim et al. | Dec 2008 | A1 |
20090002590 | Kimura | Jan 2009 | A1 |
20090008638 | Kang et al. | Jan 2009 | A1 |
20090008639 | Akimoto et al. | Jan 2009 | A1 |
20090027371 | Lin et al. | Jan 2009 | A1 |
20090045397 | Iwasaki | Feb 2009 | A1 |
20090068773 | Lai et al. | Mar 2009 | A1 |
20090073325 | Kuwabara et al. | Mar 2009 | A1 |
20090114910 | Chang | May 2009 | A1 |
20090114918 | Wang | May 2009 | A1 |
20090121233 | Yasukawa | May 2009 | A1 |
20090134399 | Sakakura et al. | May 2009 | A1 |
20090142888 | Tsuchiya | Jun 2009 | A1 |
20090152506 | Umeda et al. | Jun 2009 | A1 |
20090152541 | Maekawa et al. | Jun 2009 | A1 |
20090154262 | Tokunaga | Jun 2009 | A1 |
20090184315 | Lee et al. | Jul 2009 | A1 |
20090230435 | Maejima | Sep 2009 | A1 |
20090278122 | Hosono et al. | Nov 2009 | A1 |
20090280600 | Hosono et al. | Nov 2009 | A1 |
20090305461 | Akimoto et al. | Dec 2009 | A1 |
20100065844 | Tokunaga | Mar 2010 | A1 |
20100092800 | Itagaki et al. | Apr 2010 | A1 |
20100097838 | Tanaka et al. | Apr 2010 | A1 |
20100102397 | Park et al. | Apr 2010 | A1 |
20100109002 | Itagaki et al. | May 2010 | A1 |
20100136743 | Akimoto et al. | Jun 2010 | A1 |
20100140608 | Park et al. | Jun 2010 | A1 |
20100148171 | Hayashi et al. | Jun 2010 | A1 |
20100193785 | Kimura | Aug 2010 | A1 |
20100213531 | Asami et al. | Aug 2010 | A1 |
20100276685 | Itagaki et al. | Nov 2010 | A1 |
20100276689 | Iwasaki | Nov 2010 | A1 |
20100279462 | Iwasaki | Nov 2010 | A1 |
20110089417 | Yamazaki et al. | Apr 2011 | A1 |
20110101332 | Yamazaki et al. | May 2011 | A1 |
20110101334 | Yamazaki et al. | May 2011 | A1 |
20110101339 | Yamazaki et al. | May 2011 | A1 |
20110101351 | Yamazaki | May 2011 | A1 |
20110104851 | Akimoto et al. | May 2011 | A1 |
20110108706 | Koyama | May 2011 | A1 |
20110108836 | Koyama et al. | May 2011 | A1 |
20110110145 | Yamazaki et al. | May 2011 | A1 |
20110116310 | Yamazaki et al. | May 2011 | A1 |
20110117697 | Akimoto et al. | May 2011 | A1 |
20110121285 | Yamazaki et al. | May 2011 | A1 |
20110121286 | Yamazaki et al. | May 2011 | A1 |
20110121290 | Akimoto et al. | May 2011 | A1 |
20110122670 | Yamazaki et al. | May 2011 | A1 |
20110122673 | Kamata et al. | May 2011 | A1 |
20110128777 | Yamazaki et al. | Jun 2011 | A1 |
20110134683 | Yamazaki et al. | Jun 2011 | A1 |
20110147737 | Yamazaki et al. | Jun 2011 | A1 |
20110156027 | Yamazaki et al. | Jun 2011 | A1 |
20110156117 | Yamazaki et al. | Jun 2011 | A1 |
20110163311 | Akimoto et al. | Jul 2011 | A1 |
20110207251 | Anzai et al. | Aug 2011 | A1 |
20110299318 | Kaneko et al. | Dec 2011 | A1 |
20120057396 | Yamazaki et al. | Mar 2012 | A1 |
20120063207 | Kato et al. | Mar 2012 | A1 |
20120063209 | Koyama et al. | Mar 2012 | A1 |
20130056728 | Morosawa et al. | Mar 2013 | A1 |
20130256657 | Yamazaki et al. | Oct 2013 | A1 |
20130292677 | Yamazaki et al. | Nov 2013 | A1 |
20140138778 | Kato | May 2014 | A1 |
Number | Date | Country |
---|---|---|
1656618 | Aug 2005 | CN |
101038919 | Sep 2007 | CN |
1 737 044 | Dec 2006 | EP |
1 835 535 | Sep 2007 | EP |
2 226 847 | Sep 2010 | EP |
60-198861 | Oct 1985 | JP |
63-210022 | Aug 1988 | JP |
63-210023 | Aug 1988 | JP |
63-210024 | Aug 1988 | JP |
63-215519 | Sep 1988 | JP |
63-239117 | Oct 1988 | JP |
63-265818 | Nov 1988 | JP |
02-154388 | Jun 1990 | JP |
02-154389 | Jun 1990 | JP |
05-251705 | Sep 1993 | JP |
06-097366 | Apr 1994 | JP |
06-204424 | Jul 1994 | JP |
08-264794 | Oct 1996 | JP |
11-505377 | May 1999 | JP |
2000-044236 | Feb 2000 | JP |
2000-150900 | May 2000 | JP |
2002-076356 | Mar 2002 | JP |
2002-289859 | Oct 2002 | JP |
2003-086000 | Mar 2003 | JP |
2003-086808 | Mar 2003 | JP |
2004-103957 | Apr 2004 | JP |
2004-273614 | Sep 2004 | JP |
2004-273732 | Sep 2004 | JP |
2006-502597 | Jan 2006 | JP |
2007-096055 | Apr 2007 | JP |
2007-123861 | May 2007 | JP |
2007-294897 | Nov 2007 | JP |
2009-135350 | Jun 2009 | JP |
2009-158939 | Jul 2009 | JP |
2009-167087 | Jul 2009 | JP |
2004038757 | May 2004 | WO |
2004114391 | Dec 2004 | WO |
2010097862 | Sep 2010 | WO |
Entry |
---|
Tomoyuki Ishii et al.; “A Poly-Silicon TFT With a Sub-5-nm Thick Channel for Low-Power Gain Cell Memory in Mobile Applications”; IEEE Transactions on Electron Devices; Nov. 1, 2004; pp. 1805-1810; vol. 51, No. 11. |
Wonchan Kim et al.; “An Experimental High-Density DRAM Cell with a Built-in Gain Stage”; IEEE Journal of Solid-State Circuits; Aug. 1, 1994; pp. 978-981; vol. 29, No. 8. |
Shoji Shukuri et al.; “A Complementary Gain Cell Technology for Sub-1V Supply DRAMs”; IEDM 92: Technical Digest of International Electron Devices Meeting; Dec. 13, 1992; pp. 1006-1008. |
Shoji Shukuri et al.; “A Semi-Static Complementary Gain Cell Technology for Sub-1 V Supply DRAM's”; IEEE Transactions on Electron Devices; Jun. 1, 1994; pp. 926-931, vol. 41, No. 6. |
International Search Report, PCT Application No. PCT/JP2011/070095, dated Dec. 6, 2011, 3 pages. |
Written Opinion, PCT Application No. PCT/JP2011/070095, dated Dec. 6, 2011, 4 pages. |
Kamiya, T et al., “Carrier Transport Properties and Electronic Structures of Amorphous Oxide Semiconductors: The present status,” Kotai Butsuri (Solid State Physics), AGNE Gijutsu Center, Sep. 1, 2009, vol. 44, No. 9, pp. 621-633 with full English translation. |
Ohara, H et al., “Amorphous In-Ga-Zn-Oxide TFTs with Suppressed Variation for 4.0 inch QVGA AMOLED Display,” AM-FPD '09 Digest of Technical Papers, Jul. 1, 2009, pp. 227-230, The Japan Society of Applied Physics. |
Orita, M et al., “Amorphous transparent conductive oxide InGaO3(ZnO)m (M<4):a Zn4s conductor,” Philosophical Magazine, 2001, vol. 81, No. 5, pp. 501-515. |
Orita, M et al., “Mechanism of Electrical Conductivity of Transparent InGaZnO4,” Phys. Rev. B (Physical Review. B), Jan. 15, 2000, vol. 61, No. 3, pp. 1811-1816. |
Osada, T et al., “15.2: Development of Driver-Integrated Panel using Amorphous In-Ga-Zn-Oxide TFT,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 184-187. |
Osada, T et al., “Development of Driver-Integrated Panel Using Amorphous In-Ga-Zn-Oxide TFT,” AM-FPD '09 Digest of Technical Papers, Jul. 1, 2009, pp. 33-36. |
Park, J et al., “Dry etching of ZnO films and plasma-induced damage to optical properties,” J. Vac. Sci. Technol. B (Journal of Vacuum Science & Technology B), Mar. 1, 2003, vol. 21, No. 2, pp. 800-803. |
Park, J et al., “Improvements in the Device Characteristics of Amorphous Indium Gallium Zinc Oxide Thin-Film Transisotrys by Ar Plasma Treatment,” Appl. Phys. Lett. (Applied Physics Letters), Jun. 26, 2007, vol. 90, No. 26, pp. 262106-1-262106-3. |
Park, J et al., “Electronic Transport Properties of Amorphous Indium-Gallium-Zinc Oxide Semiconductor Upon Exposure to Water,” Appl. Phys. Lett. (Applied Physics Letters), 2008, vol. 92, pp. 072104-1-072104-3. |
Park, J et al., “High performance amorphous oxide thin film transistors with self-aligned top-gate structure,” IEDM 09: Technical Digest of International Electron Devices Meeting, Dec. 7, 2009, pp. 191-194. |
Park, Sang-Hee et al., “42.3: Transparent ZnO Thin Film Transistor for the Application of High Aperture Ratio Bottom Emission AM-OLED Display,” SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, p. 629-632. |
Park, J et al., “Amorphous Indium-Gallium-Zinc Oxide TFTS and Their Application for Large Size AMOLED,” AM-FPD '08 Digest of Technical Papers, Jul. 2, 2008, pp. 275-278. |
Park, S et al., “Challenge to Future Displays: Transparent AM-OLED Driven by Peald Grown ZnO TFT,” IMID '07 Digest, 2007, pp. 1249-1252. |
Prins, M et al., “A Ferroelectric Transparent Thin-Film Transistor,” Appl. Phys. Lett. (Applied Physics Letters), Jun. 17, 1996, vol. 68, No. 25, pp. 3650-3652. |
Sakata, J et al., “Development of 4.0-In. AMOLED Display With Driver Circuit Using Amorphous In-Ga-Zn-Oxide TFTS,” IDW'09 : Proceedings of the 16th International Display Workshops, 2009, pp. 689-692. |
Son, K et al., “42.4L: Late-News Paper: 4 Inch QVGA AMOLED Driven by the Threshold Voltage Controlled Amorphous GiZo (Ga2O3-In2O3-ZnO) TFT,” SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, pp. 633-636. |
Takahashi, M et al., “Theoretical Analysis of IGZO Transparent Amorphous Oxide Semiconductor,” IDW '08 : Proceedings of the 15th International Display Workshops, Dec. 3, 2008, pp. 1637-1640. |
Tsuda, K et al., “Ultra Low Power Consumption Technologies for Mobile TFT-LCDs,” IDW '02 : Proceedings of the 9th International Display Workshops, Dec. 4, 2002, pp. 295-298. |
Ueno, K et al., “Field-Effect Transistor on SrTiO3 With Sputtered AI2O3 Gate Insulator,” Appl. Phys. Lett. (Applied Physics Letters), Sep. 1, 2003, vol. 83, No. 9, pp. 1755-1757. |
Van De Walle, C, “Hydrogen as a Cause of Doping in Zinc Oxide,” Phys. Rev. Lett. (Physical Review Letters), Jul. 31, 2000, vol. 85, No. 5, pp. 1012-1015. |
Asakuma, N et al., “Crystallization and Reduction of Sol-Gel-Derived Zinc Oxide Films by Irradiation With Ultraviolet Lamp,” Journal of Sol-Gel Science and Technology, 2003, vol. 26, pp. 181-184. |
Asaoka, Y et al., “29.1: Polarizer-Free Reflective LCD Combined With Ultra Low-Power Driving Technology,” SID Digest '09 : SID International Symposium Digest of Technical Papers, 2009, pp. 395-398. |
Chern, H et al., “An Analytical Model for the Above-Threshold Characteristics of Polysilicon Thin-Film Transistors,” IEEE Transactions on Electron Devices, Jul. 1, 1995, vol. 42, No. 7, pp. 1240-1246. |
Cho, D et al., “21.2: AL and SN-Doped Zinc Indium Oxide Thin Film Transistors for AMOLED Back-Plane,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 280-283. |
Clark, S et al., “First Principles Methods Using Castep,” Zeitschrift fur Kristallographie, 2005, vol. 220, pp. 567-570. |
Coates. D et al., “Optical Studies of the Amorphous Liquid-Cholesteric Liquid Crystal Transition: The Blue Phase,” Physics Letters, Sep. 10, 1973, vol. 45A, No. 2, pp. 115-116. |
Costello, M et al., “Electron Microscopy of a Cholesteric Liquid Crystal and Its Blue Phase,” Phys. Rev. A (Physical Review. A), May 1, 1984, vol. 29, No. 5, pp. 2957-2959. |
Dembo, H et al., “RFCPUS on Glass and Plastic Substrates Fabricated by TFT Transfer Technology,” IEDM 05: Technical Digest of International Electron Devices Meeting, Dec. 5, 2005, pp. 1067-1069. |
Fortunato, E et al., “Wide-Bandgap High-Mobility ZnO Thin-Film Transistors Produced at Room Temperature,” Appl. Phys. Lett. (Applied Physics Letters), Sep. 27, 2004, vol. 85, No. 13, pp. 2541-2543. |
Fung, T et al., “2-D Numerical Simulation of High Performance Amorphous In-Ga-Zn-O TFTs for Flat Panel Displays,” AM-FPD '08 Digest of Technical Papers, Jul. 2, 2008, pp. 251-252, The Japan Society of Applied Physics. |
Godo, H et al., “P-9: Numerical Analysis on Temperature Dependence of Characteristics of Amorphous In-Ga-Zn-Oxide TFT,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 1110-1112. |
Godo, H et al., “Temperature Dependence of Characteristics and Electronic Structure for Amorphous In-Ga-Zn-Oxide TFT,” AM-FPD '09 Digest of Technical Papers, Jul. 1, 2009, pp. 41-44. |
Hayashi, R et al., “42.1: Invited Paper: Improved Amorphous In-Ga-Zn-O TFTS,” SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, pp. 621-624. |
Hirao, T et al., “Novel Top-Gate Zinc Oxide Thin-Film Transistors (ZnO TFTS) for AMLCDS,” Journal of the SID , 2007, vol. 15, No. 1, pp. 17-22. |
Hosono, H et al., “Working hypothesis to explore novel wide band gap electrically conducting amorphous oxides and examples,” J. Non-Cryst. Solids (Journal of Non-Crystalline Solids), 1996, vol. 198-200, pp. 165-169. |
Hosono, H, “68.3: Invited Paper:Transparent Amorphous Oxide Semiconductors for High Performance TFT,” SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1830-1833. |
Hsieh, H et al., “P-29: Modeling of Amorphous Oxide Semiconductor Thin Film Transistors and Subgap Density of States,” SID Digest '08 : SID International Symposium Digest of Technical Papers, 2008, vol. 39, pp. 1277-1280. |
Ikeda., T et al., “Full-Functional System Liquid Crystal Display Using CG-Silicon Technology,” SID Digest '04 : SID International Symposium Digest of Technical Papers, 2004, vol. 35, pp. 860-863. |
Janotti, A et al., “Native Point Defects in ZnO,” Phys. Rev. B (Physical Review. B), 2007, vol. 76, No. 16, pp. 165202-1-165202-22. |
Janotti, A et al., “Oxygen Vacancies in ZnO,” Appl. Phys. Lett. (Applied Physics Letters), 2005, vol. 87, pp. 122102-1-122102-3. |
Jeong, J et al., “3.1: Distinguished Paper: 12.1-Inch WXGA AMOLED Display Driven by Indium-Gallium-Zinc Oxide TFTs Array,” SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, No. 1, pp. 1-4. |
Jin, D et al., “65.2: Distinguished Paper:World-Largest (6.5″) Flexible Full Color Top Emission AMOLED Display on Plastic Film and Its Bending Properties,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 983-985. |
Kanno, H et al., “White Stacked Electrophosphorecent Organic Light-Emitting Devices Employing MOO3 As a Charge-Generation Layer,” Adv. Mater. (Advanced Materials), 2006, vol. 18, No. 3, pp. 339-342. |
Kikuchi, H et al., “39.1: Invited Paper: Optically Isotropic Nano-Structured Liquid Crystal Composites for Display Applications,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 578-581. |
Kikuchi, H et al., “62.2: Invited Paper: Fast Electro-Optical Switching in Polymer-Stabilized Liquid Crystalline Blue Phases for Display Application,” SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1737-1740. |
Kikuchi, H et al., “Polymer-Stabilized Liquid Crystal Blue Phases,” Nature Materials, Sep. 1, 2002, vol. 1, pp. 64-68. |
Kim, S et al., “High-Performance oxide thin film transistors passivated by various gas plasmas,” The Electrochemical Society, 214th ECS Meeting, 2008, No. 2317, 1 page. |
Kimizuka, N. et al., “Spinel,YBFE2O4, and YB2FE3O7 Types of Structures for Compounds in the IN2O3 and SC2O3-A2O3-Bo Systems [A; Fe, Ga, or Al; B: Mg, Mn, Fe, Ni, Cu,or Zn] at Temperatures Over 1000 ° C.”, Journal of Solid State Chemistry, 1985, vol. 60, pp. 382-384. |
Kimizuka, N. et al., “Syntheses and Single-Crystal Data of Homologous Compounds, In2O3(ZnO)m (m=3, 4, and 5), InGaO3(ZnO)3, and Ga2O3(ZnO)m (m=7, 8, 9, and 16) in the In2O3-ZnGa2O4-ZnO System,” Journal of Solid State Chemistry, Apr. 1, 1995, vol. 116, No. 1, pp. 170-178. |
Kitzerow, H et al., “Observation of Blue Phases in Chiral Networks,” Liquid Crystals, 1993, vol. 14, No. 3, pp. 911-916. |
Kurokawa, Y et al., “UHF RFCPUS on Flexible and Glass Substrates for Secure RFID Systems,” Journal of Solid-State Circuits , 2008, vol. 43, No. 1, pp. 292-299. |
Lany, S et al., “Dopability, Intrinsic Conductivity, and Nonstoichiometry of Transparent Conducting Oxides,” Phys. Rev. Lett. (Physical Review Letters), Jan. 26, 2007, vol. 98, pp. 045501-1-045501-4. |
Lee, H et al., “Current Status of, Challenges to, and Perspective View of AM-OLED,” IDW '06 : Proceedings of the 13th International Display Workshops, Dec. 7, 2006, pp. 663-666. |
Lee, J et al., “World'S Largest (15-Inch) XGA AMLCD Panel Using IGZO Oxide TFT,” SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, pp. 625-628. |
Lee, M et al., “15.4: Excellent Performance of Indium-Oxide-Based Thin-Film Transistors by DC Sputtering,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 191-193. |
Li, C et al “Modulated Structures of Homologous Compounds InMO3(ZnO)m (M=In,Ga; m=Integer) Described by Four-Dimensional Superspace Group,” Journal of Solid State Chemistry, 1998, vol. 139, pp. 347-355. |
Masuda, S et al., “Transparent thin film transistors using ZnO as an active channel layer and their electrical properties,” J. Appl. Phys. (Journal of Applied Physics), Feb. 1, 2003, vol. 93, No. 3, pp. 1624-1630. |
Meiboom, S et al., “Theory of the Blue Phase of Cholesteric Liquid Crystals,” Phys. Rev. Lett. (Physical Review Letters), May 4, 1981, vol. 46, No. 18, pp. 1216-1219. |
Miyasaka, M, “Suftla Flexible Microelectronics on Their Way to Business,” SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1673-1676. |
Mo, Y et al., “Amorphous Oxide TFT Backplanes for Large Size AMOLED Displays,” IDW '08 : Proceedings of the 6th International Display Workshops, Dec. 3, 2008, pp. 581-584. |
Nakamura, “Synthesis of Homologous Compound with New Long-Period Structure,” NIRIM Newsletter, Mar. 1995, vol. 150, pp. 1-4 with English Translation. |
Nakamura, M et al., “The phase relations in the In2O3-Ga2ZnO4-ZnO system at 1350 ° C.,” Journal of Solid State Chemistry, Aug. 1, 1991, vol. 93, No. 2, pp. 298-315. |
Nomura, K et al., “Thin-Film Transistor Fabricated in Single-Crystalline Transparent Oxide Semiconductor,” Science, May 23, 2003, vol. 300, No. 5623, pp. 1269-1272. |
Nomura, K et al., “Amorphous Oxide Semiconductors for High-Performance Flexible Thin-Film Transistors,” Jpn. J. Appl. Phys. (Japanese Journal of Applied Physics) , 2006, vol. 45, No. 5B, pp. 4303-4308. |
Nomura, K et al., “Room-Temperature Fabrication of Transparent Flexible Thin-Film Transistors Using Amorphous Oxide Semiconductors,” Nature, Nov. 25, 2004, vol. 432, pp. 488-492. |
Nomura, K et al., “Carrier transport in transparent oxide semiconductor with intrinsic structural randomness probed using single-crystalline InGaO3(ZnO)5 films,” Appl. Phys. Lett. (Applied Physics Letters) , Sep. 13, 2004, vol. 85, No. 11, pp. 1993-1995. |
Nowatari, H et al., “60.2: Intermediate Connector with Suppressed Voltage Loss for White Tandem OLEDS,” SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, vol. 40, pp. 899-902. |
Oba, F et al., “Defect energetics in ZnO: A hybrid Hartree-Fock density functional study,” Phys. Rev. B (Physical Review. B), 2008, vol. 77, pp. 245202-1-245202-6. |
Oh, M et al., “Improving the Gate Stability of ZnO Thin-Film Transistors With Aluminum Oxide Dielectric Layers,” J. Electrochem. Soc. (Journal of the Electrochemical Society), 2008, vol. 155, No. 12, pp. H1009-H1014. |
Ohara, H et al., “21.3: 4.0 In. QVGA AMOLED Display using In-Ga-Zn-Oxide TFTS with a Novel Passivation Layer,” SID Digest '09 : SID Internatinoal Symposium Digest of Technical Papers, May 31, 2009, pp. 284-287. |
Number | Date | Country | |
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20120063208 A1 | Mar 2012 | US |