The present invention relates generally to semiconductor devices, and more particularly to integrated circuits including non-volatile semiconductor memories and methods of fabricating the same.
Non-volatile semiconductor memories are devices that can be electrically erased and reprogrammed. One type of non-volatile memory that is widely used for general storage and transfer of data in and between computers and other electronic devices is flash memory, such as a split gate flash memory. A split gate flash memory transistor has an architecture similar to that of a conventional logic transistor, such as Metal-Oxide-Semiconductor Field Effect Transistor (MOSFET), in that it also includes a control gate formed over a channel connecting a source and drain in a substrate. However, the memory transistor further includes a memory or charge trapping layer between the control gate and the channel and insulated from both by insulating or dielectric layers. A programming voltage applied to the control gate traps a charge on the charge trapping layer, partially canceling or screening an electric field from the control gate, thereby changing a threshold voltage (VT) of the transistor and programming the memory cell. During read-out, this shift in VT is sensed by the presence or absence of current flow through the channel with application of a predetermined read-out voltage. To erase the memory transistor, an erase voltage is applied to the control gate to restore, or reverse the shift in VT.
An important measure of merit for flash memories is data retention time, which is the time for which the memory transistor can hold charge or remain programmed without the application of power. The charge stored or trapped in the charge trapping layer decreases over time due to leakage current through the insulating layers, thereby reducing the difference between a programmed threshold voltage (VTP) and an erased threshold voltage (VTE) limiting data retention of the memory transistor.
One problem with conventional memory transistors and methods of forming the same is that the charge trapping layer typically has poor or decreasing data retention over time, limiting the useful transistor lifetime. Referring to
Referring to
Another problem is that increasingly semiconductor memories combine logic transistors, such as MOSFET's, with memory transistors in integrated circuits (ICs) fabricated on a common substrate for embedded memory or System-On-Chip (SOC) applications. Many of the current processes for forming performance of memory transistors are incompatible with those used for fabricating logic transistors.
Accordingly, there is a need for memory transistors and methods of forming the same that provides improved data retention and increased transistor lifetime. It is further desirable that the methods of forming the memory device are compatible with those for forming logic elements in the same IC formed on a common substrate.
The present invention provides a solution to these and other problems, and offers further advantages over conventional memory cells or devices and methods of fabricating the same.
Generally, the device includes a memory transistor comprising a polysilicon channel region electrically connecting a source region and a drain region formed in a substrate, an oxide-nitride-nitride-oxide (ONNO) stack disposed above the channel region, and a high work function gate electrode formed over a surface of the ONNO stack. In one embodiment, the ONNO stack includes a multi-layer charge-trapping region including an oxygen-rich first nitride layer and an oxygen-lean second nitride layer disposed above the first nitride layer. In another embodiment, the multi-layer charge-trapping region further includes an oxide anti-tunneling layer separating the first nitride layer from the second nitride layer.
These and various other features and advantages of the present invention will be apparent upon reading of the following detailed description in conjunction with the accompanying drawings and the appended claims provided below, where:
The present invention is directed generally to non-volatile memory transistor including a multi-layer charge storage layer and high work function gate electrode to increase data retention and/or to improve programming time and efficiency. The structure and method are particularly useful for embedded memory or System-On-Chip (SOC) applications in which a semiconductor device includes both a logic transistor and non-volatile memory transistor comprising high work function gate electrodes formed on a common substrate.
In the following description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the present invention. It will be evident, however, to one skilled in the art that the present invention may be practiced without these specific details. In other instances, well-known structures, and techniques are not shown in detail or are shown in block diagram form in order to avoid unnecessarily obscuring an understanding of this description.
Reference in the description to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the invention. The appearances of the phrase “in one embodiment” in various places in the specification do not necessarily all refer to the same embodiment. The term “to couple” as used herein may include both to directly connect and to indirectly connect through one or more intervening components.
Briefly, a non-volatile memory transistor according to the present invention includes a high work function gate electrode formed over an oxide-nitride-oxide (ONO) dielectric stack. By high work function gate electrode it is meant that the minimum energy needed to remove an electron from the gate electrode is increased.
In certain preferred embodiments, the high work function gate electrode comprises a doped polycrystalline silicon or polysilicon (poly) layer, the fabrication of which can be can be readily integrated into standard complementary metal-oxide-semiconductor (CMOS) process flows, such as those used fabricate metal-oxide-semiconductor (MOS) logic transistors, to enable fabrication of semiconductor memories or devices including both memory and logic transistors. More preferably, the same doped polysilicon layer can also be patterned to form a high work function gate electrode for the MOS logic transistor, thereby improving the performance of the logic transistor and increasing the efficiency of the fabrication process. Optionally, the ONO dielectric stack includes a multi-layer charge storage or charge trapping layer to further improve performance, and in particular data retention, of the memory transistor.
A semiconductor device including a non-volatile memory transistor comprising a high work function gate electrode and methods of forming the same will now be described in detail with reference to
Referring to
Generally, the substrate 206 may include any known silicon-based semiconductor material including silicon, silicon-germanium, silicon-on-insulator, or silicon-on-sapphire substrate. Alternatively, the substrate 206 may include a silicon layer formed on a non-silicon-based semiconductor material, such as gallium-arsenide, germanium, gallium-nitride, or aluminum-phosphide. Preferably, the substrate 206 is a doped or undoped silicon substrate.
The lower oxide layer or tunneling oxide layer 208 of the ONO dielectric stack 202 generally includes a relatively thin layer of silicon dioxide (SiO2) of from about 15 angstrom (Å) to about 22 Å, and more preferably about 18 Å. The tunneling oxide layer 208 can be formed or deposited by any suitable means including, for example, being thermally grown or deposited using chemical vapor deposition (CVD). In a preferred embodiment, the tunnel dielectric layer is formed or grown using a steam anneal. Generally, the process includes a wet-oxidizing method in which the substrate 206 is placed in a deposition or processing chamber, heated to a temperature from about 700° C. to about 850° C., and exposed to a wet vapor for a predetermined period of time selected based on a desired thickness of the finished tunneling oxide layer 208. Exemplary process times are from about 5 to about 20 minutes. The oxidation can be performed at atmospheric or at low pressure.
In a preferred embodiment, the oxynitride layers 210A, 210B, of the multi-layer charge storage layer 210 are formed or deposited in separate steps utilizing different processes and process gases or source materials, and have an overall or combined thickness of from about 70 Å to about 150 Å, and more preferably about 100 Å. The lower, trap free oxynitride layer 210B can be formed or deposited by any suitable means including, for example, deposition in a low pressure CVD process using a process gas including a silicon source, such as silane (SiH4), chlorosilane (SiH3Cl), dichlorosilane (SiH2Cl2), tetrachlorosilane (SiCl4), a nitrogen source, such as nitrogen (N2), ammonia (NH3), nitrogen trioxide (NO3) or nitrous oxide (N2O), and an oxygen-containing gas, such as oxygen (O2) or N2O. In one embodiment the trap free oxynitride layer 210B is deposited in a low pressure CVD process using a process gas including dichlorosilane, NH3 and N2O, while maintaining the chamber at a pressure of from about 5 millitorr (mT) to about 500 mT, and maintaining the substrate at a temperature of from about 700° C. to about 850° C. and more preferably at least about 780° C., for a period of from about 2.5 minutes to about 20 minutes. In particular, the process gas can include a first gas mixture of N2O and NH3 mixed in a ratio of from about 8:1 to about 1:8 and a second gas mixture of DCS and NH3 mixed in a ratio of from about 1:7 to about 7:1, and can be introduced at a flow rate of from about 5 to about 200 standard cubic centimeters per minute (sccm).
The top, charge trapping oxynitride layer 210A can be deposited over the bottom oxynitride layer 210B in a CVD process using a process gas including Bis-TertiaryButylAminoSilane (BTBAS). It has been found that the use of BTBAS increases the number of deep traps formed in the oxynitride by increasing the carbon level in the charge trapping oxynitride layer 210A. Moreover, these deep traps reduce charge losses due to thermal emission, thereby further improving data retention. More preferably, the process gas includes BTBAS and ammonia (NH3) mixed at a predetermined ratio to provide a narrow band gap energy level in the oxynitride charge trapping layer. In particular, the process gas can include BTBAS and NH3 mixed in a ratio of from about 7:1 to about 1:7. For example, in one embodiment the charge trapping oxynitride layer 210A is deposited in a low pressure CVD process using BTBAS and ammonia NH3 at a chamber pressure of from about 5 mT to about 500 mT, and at a substrate temperature of from about 700° C. to about 850° C. and more preferably at least about 780° C., for a period of from about 2.5 minutes to about 20 minutes.
It has been found that an oxynitride layer produced or deposited under the above conditions yields a trap-rich oxynitride layer 210A, which improves the program and erase speed and increases of the initial difference (window) between program and erase voltages without compromising a charge loss rate of the memory transistor, thereby extending the operating life (EOL) of the device. Preferably, the charge trapping oxynitride layer 210A has a charge trap density of at least about 1E10/cm2, and more preferably from about 1E12/cm2 to about 1E14/cm2.
Alternatively, the charge trapping oxynitride layer 210A can be deposited over the bottom oxynitride layer 210B in a CVD process using a process gas including BTBAS and substantially not including ammonia (NH3). In this alternative embodiment of the method, the step of depositing the top, charge trapping oxynitride layer 210A is followed by a thermal annealing step in a nitrogen atmosphere including nitrous oxide (N2O), NH3, and/or nitrogen oxide (NO).
Preferably, the top, charge trapping oxynitride layer 210A is deposited sequentially in the same CVD tool used to form the bottom, trap free oxynitride layer 210B, substantially without breaking vacuum on the deposition chamber. More preferably, the charge trapping oxynitride layer 210A is deposited substantially without altering the temperature to which the substrate 206 was heated during deposition of the trap free oxynitride layer 210B.
A suitable thickness for the lower, trap free oxynitride layer 210B has been found to be from about 10 Å to about 80 Å, and a ratio of thicknesses between the bottom layer and the top, charge trapping oxynitride layer has been found to be from about 1:6 to about 6:1, and more preferably at least about 1:4.
The top oxide layer 212 of the ONO dielectric stack 202 includes a relatively thick layer of SiO2 of from about 20 Å to about 70 Å, and more preferably about 45 Å. The top oxide layer 212 can be formed or deposited by any suitable means including, for example, being thermally grown or deposited using CVD. In a preferred embodiment, the top oxide layer 212 is a high-temperature-oxide (HTO) deposited using CVD process. Generally, the deposition process includes exposing the substrate 306 to a silicon source, such as silane, chlorosilane, or dichlorosilane, and an oxygen-containing gas, such as O2 or N2O in a deposition chamber at a pressure of from about 50 mT to about 1000 mT, for a period of from about 10 minutes to about 120 minutes while maintaining the substrate at a temperature of from about 650° C. to about 850° C.
Preferably, the top oxide layer 212 is deposited sequentially in the same tool used to form the oxynitride layers 210A, 210B. More preferably, the oxynitride layers 210A, 210B, and the top oxide layer 212 are formed or deposited in the same tool used to grow the tunneling oxide layer 208. Suitable tools include, for example, an ONO AVP, commercially available from AVIZA technology of Scotts Valley, Calif.
Referring to
Generally, the ONO dielectric stack 202 is removed from the desired region or area of the surface 204 using standard photolithographic and oxide etch techniques. For example, in one embodiment a patterned mask layer (not shown) is formed from a photo-resist deposited on the ONO dielectric stack 202, and the exposed region etched or removed using a low pressure radiofrequency (RF) coupled or generated plasma comprising fluorinated hydrocarbon and/or fluorinated carbon compounds, such as C2H2F4 commonly referred to as Freon®. Generally, the processing gas further includes argon (Ar) and nitrogen (N2) at flow rates selected to maintain a pressure in the etch chamber of from about 50 mT to about 250 mT during processing.
The oxide layer 214 of the logic transistor can include a layer of SiO2 having a thickness of from about 30 to about 70 Å, and can be thermally grown or deposited using CVD. In one embodiment, the oxide layer 214 is thermally grown using a steam oxidation process, for example, by maintaining the substrate 206 in a steam atmosphere at a temperature of from about 650° C. to about 850° C. for a period of from about 10 minutes to about 120 minutes.
Next, a doped polysilicon layer is formed on a surface of the ONO dielectric stack 202 and, preferably, the oxide layer 214 of the logic transistor. More preferably, the substrate 206 is a silicon substrate or has a silicon surface on which the ONO dielectric stack is formed to form a silicon-oxide-nitride-oxide-silicon (SONOS) gate stack of a SONOS memory transistor.
Referring to
In one embodiment, the polysilicon layer 216 is doped following the growth or formation in the LPCVD process using ion implantation process. For example, the polysilicon layer 216 can be doped by implanting boron (B+) or BF2 ions at an energy of from about 5 to about 100 kilo-electron volts (keV), and a dose of from about 1e14 cm−2 to about 1e16 cm−2 to form an N-type (NMOS) SONOS memory transistor and, preferably, a P-type (PMOS) logic transistor having high work function gate electrodes. More preferably, the polysilicon layer 216 is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 electron volts (eV) to about 5.3 eV.
Alternatively, the polysilicon layer 216 can be doped by ion implantation after patterning or etching the polysilicon layer and the underlying dielectric layers. It will be appreciated that this embodiment includes additional masking steps to protect exposed areas of the substrate 206 surface 204 and/or the dielectric layers from receiving undesired doping. However, generally such a masking step is included in existing process flows regardless of whether the implantation occurs before or after patterning.
Referring to
Finally, the substrate is thermal annealed with a single or multiple annealing steps at a temperature of from about 800° C. to about 1050° C. for a time of from about 1 second to about 5 minutes to drive in ions implanted in the polysilicon layer 216, and to repair damage to the crystal structure of the polysilicon layer caused by ion implantation. Alternatively, advanced annealing techniques, such as flash and laser, can be employed with temperatures as high as 1350° C. and anneal times as low as 1 millisecond.
A partial cross-sectional side view of a semiconductor device 300 including a logic transistor 302 and non-volatile memory transistor 304 comprising high work function gate electrodes according to an embodiment of the present invention is shown in
The logic transistor 302 comprises a gate electrode 324 overlying an oxide layer 326 formed over a channel region 328 separating heavily doped source and drain regions 330, and, optionally, can include one or more sidewall spacers 332 surrounding the gate electrically insulate it from contacts (not shown) to the S/D regions. Preferably, as shown in
Generally, the semiconductor device 300 further includes a number of isolation structures 334, such as a local oxidation of silicon (LOCOS) region or structure, a field oxidation region or structure (FOX), or a shallow trench isolation (STI) structure to electrically isolate individual transistors formed on the substrate 306 from one another.
Implementations and Alternatives
In one aspect the present disclosure is directed to semiconductor devices including memory transistors with a high work function gate electrode and a multi-layer charge-trapping region.
The nanowire channel region 412 can comprise polysilicon or recrystallized polysilicon to form a monocrystalline channel region. Optionally, where the channel region 412 includes a crystalline silicon, the channel region can be formed to have <100> surface crystalline orientation relative to a long axis of the channel region.
The high work function gate electrode 414 includes a doped polysilicon layer formed or deposited in a low pressure CVD process and having a thickness of from about 200 Å to about 2000 Å. As noted above, the polysilicon layer of the high work function gate electrode 414 can be formed or grown directly as a doped polysilicon layer through the addition of gases such as phosphine, arsine, diborane or difluoroborane (BF2) to the CVD chamber during the low pressure CVD process, or can be doped following the growth or formation in the CVD process using an ion implantation process. In either embodiment, the polysilicon layer of the high work function gate electrode 414 is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 electron volts (eV) to about 5.3 eV. In an exemplary embodiment, the polysilicon layer of the high work function gate electrode 414 is doped by implanting boron (B+) or BF2 ions at an energy of from about 5 to about 100 kilo-electron volts (keV), and a dose of from about 1e14 cm−2 to about 1e16 cm−2 to form an N-type (NMOS) memory transistor.
The tunnel dielectric layer 416 may be any material and have any thickness suitable to allow charge carriers to tunnel into the multi-layer charge-trapping region 422 under an applied gate bias while maintaining a suitable barrier to leakage when the memory transistor 400 is unbiased. In one embodiment, the tunnel dielectric layer 416 is formed by a thermal oxidation process and is composed of silicon dioxide or silicon oxy-nitride, or a combination thereof. In another embodiment, the tunnel dielectric layer 416 is formed by chemical vapor deposition (CVD) or atomic layer deposition (ALD) and is composed of a dielectric layer which may include, but is not limited to, silicon nitride, hafnium oxide, zirconium oxide, hafnium silicate, hafnium oxy-nitride, hafnium zirconium oxide and lanthanum oxide. In a specific embodiment, the tunnel dielectric layer 416 has a thickness in the range of 1-10 nanometers. In a particular embodiment, the tunnel dielectric layer 416 has a thickness of approximately 2 nanometers.
In one embodiment, the blocking dielectric layer 420 comprises a high temperature oxide (HTO). The higher quality HTO oxide enables the blocking dielectric layer 420 to be scaled in thickness. In an exemplary embodiment, the thickness of the blocking dielectric layer 420 comprising a HTO oxide is between 2.5 nm and 10.0 nm.
In another embodiment, the blocking dielectric layer 420 is further modified to incorporate nitrogen. In one such embodiment, the nitrogen is incorporated in the form of an ONO stack across the thickness of the blocking dielectric layer 420. Such a sandwich structure in place of the conventional pure oxygen blocking dielectric layer advantageously reduces the EOT of the entire stack 402 between the channel region 412 and high work function gate electrode 414 as well as enable tuning of band offsets to reduce back injection of carriers. The ONO stack blocking dielectric layer 420 can then be incorporated with the tunnel dielectric layer 416 and the multi-layer charge trapping layer 422 comprising an oxygen-rich first nitride layer 422a, an oxygen-lean second nitride layer 422b and an anti-tunneling layer 422c.
The multi-layer charge-trapping region 422 generally includes at least two nitride layers having differing compositions of silicon, oxygen and nitrogen, including an oxygen-rich, first nitride layer 422a, and a silicon-rich, nitrogen-rich, and oxygen-lean second nitride layer 422b, a silicon-rich. In some embodiments, such as that shown in
It has been found that an oxygen-rich, first nitride layer 422a decreases the charge loss rate after programming and after erase, which is manifested in a small voltage shift in the retention mode, while a silicon-rich, nitrogen-rich, and oxygen-lean second nitride layer 422b improves the speed and increases of the initial difference between program and erase voltage without compromising a charge loss rate of memory transistors made using an embodiment of the silicon-oxide-oxynitride-oxide-silicon structure, thereby extending the operating life of the device.
It has further been found the anti-tunneling layer 422c substantially reduces the probability of electron charge that accumulates at the boundaries of the oxygen-lean second nitride layer 422b during programming from tunneling into the first nitride layer 422a, resulting in lower leakage current than for a conventional non-volatile memory transistor.
The multi-layer charge-trapping region can have an overall thickness of from about 50 Å to about 150 Å, and in certain embodiments less than about 100 Å, with the with the thickness of the anti-tunneling layer 422c being from about 5 Å to about 20 Å, and the thicknesses of the nitride layers 404b, 404a, being substantially equal.
A method or forming or fabricating a semiconductor device including a memory transistor with a high work function gate electrode and a multi-layer charge-trapping region according to one embodiment will now be described with reference to the flowchart of
Referring to
Next, an oxygen-rich first nitride layer of the multi-layer charge-trapping region is formed on a surface of the tunnel dielectric layer (502). In one embodiment, the oxygen-rich first nitride layer is formed or deposited in a low pressure CVD process using a silicon source, such as silane (SiH4), chlorosilane (SiH3Cl), dichlorosilane or DCS (SiH2Cl2), tetrachlorosilane (SiCl4) or Bis-TertiaryButylAmino Silane (BTBAS), a nitrogen source, such as nitrogen (N2), ammonia (NH3), nitrogen trioxide (NO3) or nitrous oxide (N2O), and an oxygen-containing gas, such as oxygen (O2) or N2O. Alternatively, gases in which hydrogen has been replaced by deuterium can be used, including, for example, the substitution of deuterated-ammonia (ND3) for NH3. The substitution of deuterium for hydrogen advantageously passivates Si dangling bonds at the silicon-oxide interface, thereby increasing an NBTI (Negative Bias Temperature Instability) lifetime of the devices.
For example, the lower or oxygen-rich first nitride layer can be deposited over the tunnel dielectric layer by placing the substrate in a deposition chamber and introducing a process gas including N2O, NH3 and DCS, while maintaining the chamber at a pressure of from about 5 milliTorr (mT) to about 500 mT, and maintaining the substrate at a temperature of from about 700 degrees Celsius to about 850 degrees Celsius and in certain embodiments at least about 760 degrees Celsius, for a period of from about 2.5 minutes to about 20 minutes. In particular, the process gas can include a first gas mixture of N2O and NH3 mixed in a ratio of from about 8:1 to about 1:8 and a second gas mixture of DCS and NH3 mixed in a ratio of from about 1:7 to about 7:1, and can be introduced at a flow rate of from about 5 to about 200 standard cubic centimeters per minute (sccm). It has been found that an oxynitride layer produced or deposited under these condition yields a silicon-rich, oxygen-rich first nitride layer.
Next, an anti-tunneling layer is formed or deposited on a surface of the first nitride layer (504). As with the tunnel dielectric layer, the anti-tunneling layer can be formed or deposited by any suitable means, including a plasma oxidation process, In-Situ Steam Generation (ISSG) or a radical oxidation process. In one embodiment, the radical oxidation process involves flowing hydrogen (H2) and oxygen (O2) gas into a batch-processing chamber or furnace to effect growth of the anti-tunneling layer by oxidation consumption of a portion of the first nitride layer.
The top or oxygen-lean second nitride layer of the multi-layer charge-trapping region is then formed on a surface of the anti-tunneling layer (506). The oxygen-lean second nitride layer can be deposited over the anti-tunneling layer in a CVD process using a process gas including N2O, NH3 and DCS, at a chamber pressure of from about 5 mT to about 500 mT, and at a substrate temperature of from about 700 degrees Celsius to about 850 degrees Celsius and in certain embodiments at least about 760 degrees Celsius, for a period of from about 2.5 minutes to about 20 minutes. In particular, the process gas can include a first gas mixture of N2O and NH3 mixed in a ratio of from about 8:1 to about 1:8 and a second gas mixture of DCS and NH3 mixed in a ratio of from about 1:7 to about 7:1, and can be introduced at a flow rate of from about 5 to about 20 sccm. It has been found that a nitride layer produced or deposited under these condition yields a silicon-rich, nitrogen-rich, and oxygen-lean second nitride layer, which improves the speed and increases of the initial difference between program and erase voltage without compromising a charge loss rate of memory transistors made using an embodiment of the silicon-oxide-oxynitride-oxide-silicon structure, thereby extending the operating life of the device.
In some embodiments, the oxygen-lean second nitride layer can be deposited over the anti-tunneling layer in a CVD process using a process gas including BTBAS and ammonia (NH3) mixed at a ratio of from about 7:1 to about 1:7 to further include a concentration of carbon selected to increase the number of traps therein. The selected concentration of carbon in the second oxynitride layer can include a carbon concentration of from about 5% to about 15%.
Next, a top, blocking oxide layer or blocking dielectric layer is formed on a surface of the oxygen-lean second nitride layer of the multi-layer charge-trapping region (508). As with the tunnel dielectric layer and the anti-tunneling layer the blocking dielectric layer can be formed or deposited by any suitable means, including a plasma oxidation process, In-Situ Steam Generation (ISSG) or a radical oxidation process. In one embodiment, the blocking dielectric layer comprises a high-temperature-oxide (HTO) deposited using CVD process. Generally, the deposition process includes exposing the substrate 306 to a silicon source, such as silane, chlorosilane, or dichlorosilane, and an oxygen-containing gas, such as O2 or N2O in a deposition chamber at a pressure of from about 50 mT to about 1000 mT, for a period of from about 10 minutes to about 120 minutes while maintaining the substrate at a temperature of from about 650° C. to about 850° C.
Alternatively, the blocking dielectric layer is formed using an ISSG oxidation process. In one embodiment, the ISSG is performed in an RTP chamber, such as the ISSG chamber from Applied Materials described above, at pressures of from about 8 to 12 Torr and a temperature of about 1050° C. with an oxygen rich gas mixture hydrogen to which from about 0.5% to 33% hydrogen has been added.
It will be appreciated that in either embodiment the thickness of the second nitride layer may be adjusted or increased as some of the oxygen-lean second nitride layer will be effectively consumed or oxidized during the process of forming the blocking dielectric layer.
Finally, a high work function gate electrode is formed upon and in contact with the blocking dielectric layer (510). The high work function gate electrode includes a doped polysilicon layer formed or deposited in a low pressure CVD process and having a thickness of from about 200 Å to about 2000 Å. As noted above, the polysilicon layer of the high work function gate electrode can be formed or grown directly as a doped polysilicon layer through the addition of gases such as phosphine, arsine, diborane or difluoroborane (BF2) to the CVD chamber during the low pressure CVD process, or can be doped following the growth or formation in the CVD process using an ion implantation process. In either embodiment, the polysilicon layer of the high work function gate electrode is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 electron volts (eV) to about 5.3 eV. In an exemplary embodiment, the polysilicon layer of the high work function gate electrode is doped by implanting boron (B+) or BF2 ions at an energy of from about 5 to about 100 kilo-electron volts (keV), and a dose of from about 1e14 cm−2 to about 1e16 cm−2 to form an N-type (NMOS) memory transistor.
With the completion of the gate stack fabrication, further processing may occur as known in the art to conclude fabrication of a SONOS-type memory device.
In another aspect the present disclosure is also directed to multigate or multigate-surface memory transistors including charge-trapping regions overlying two or more sides of a channel region formed on or above a surface of a substrate, and methods of fabricating the same. Multigate devices include both planar and non-planar devices. A planar multigate device (not shown) generally includes a double-gate planar device in which a number of first layers are deposited to form a first gate below a subsequently formed channel region, and a number of second layers are deposited thereover to form a second gate. A non-planar multigate device generally includes a horizontal or vertical channel region formed on or above a surface of a substrate and surrounded on three or more sides by a gate.
In accordance with the present disclosure, the non-planar multigate memory transistor 600 of
As with the embodiments described above, the high work function gate electrode 614 includes a doped polysilicon layer formed or deposited in a low pressure CVD process and having a thickness of from about 200 Å to about 2000 Å. The polysilicon layer of the high work function gate electrode 614 can be formed or grown directly as a doped polysilicon layer through the addition of gases such as phosphine, arsine, diborane or BF2, and is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 eV to about 5.3 eV. In an exemplary embodiment, the polysilicon layer of the high work function gate electrode 614 is doped to a concentration of from about 1e14 cm−2 to about 1e16 cm−2.
Referring to
In one embodiment, the blocking dielectric 620 also includes an oxide, such as an HTO, to provide an ONNO structure. The channel region 602 and the overlying ONNO structure can be formed directly on a silicon substrate 606 and overlaid with a high work function gate electrode 614 to provide a SONNOS structure.
In some embodiments, such as that shown in
As with the embodiments described above, either or both of the oxygen-rich first nitride layer 616a and the oxygen-lean second nitride layer 616b can include silicon nitride or silicon oxynitride, and can be formed, for example, by a CVD process including N2O/NH3 and DCS/NH3 gas mixtures in ratios and at flow rates tailored to provide a silicon-rich and oxygen-rich oxynitride layer. The second nitride layer of the multi-layer charge storing structure is then formed on the middle oxide layer. The oxygen-lean second nitride layer 616b has a stoichiometric composition of oxygen, nitrogen and/or silicon different from that of the oxygen-rich first nitride layer 616a, and may also be formed or deposited by a CVD process using a process gas including DCS/NH3 and N2O/NH3 gas mixtures in ratios and at flow rates tailored to provide a silicon-rich, oxygen-lean top nitride layer.
In those embodiments including an intermediate or anti-tunneling layer 616c including oxide, the anti-tunneling layer can be formed by oxidation of the bottom oxynitride layer, to a chosen depth using radical oxidation. Radical oxidation may be performed, for example, at a temperature of 1000-1100 degrees Celsius using a single wafer tool, or 800-900 degrees Celsius using a batch reactor tool. A mixture of H2 and O2 gasses may be employed at a pressure of 300-500 Tor for a batch process, or 10-15 Tor using a single vapor tool, for a time of 1-2 minutes using a single wafer tool, or 30 min-1 hour using a batch process.
Finally, in those embodiments including a blocking dielectric 620 including oxide the oxide may be formed or deposited by any suitable means. In one embodiment the oxide of the blocking dielectric 620 is a high temperature oxide deposited in a HTO CVD process. Alternatively, the blocking dielectric 620 or blocking oxide layer may be thermally grown, however it will be appreciated that in this embodiment the top nitride thickness may be adjusted or increased as some of the top nitride will be effectively consumed or oxidized during the process of thermally growing the blocking oxide layer. A third option is to oxidize the second nitride layer to a chosen depth using radical oxidation.
A suitable thickness for the oxygen-rich first nitride layer 616a may be from about 30 Å to about 160 Å (with some variance permitted, for example ±10 A), of which about 5-20 Å may be consumed by radical oxidation to form the anti-tunneling layer 616c. A suitable thickness for the oxygen-lean second nitride layer 616b may be at least 30 Å. In certain embodiments, the oxygen-lean second nitride layer 616b may be formed up to 130 Å thick, of which 30-70 Å may be consumed by radical oxidation to form the blocking dielectric 620. A ratio of thicknesses between the oxygen-rich first nitride layer 616a and oxygen-lean second nitride layer 616b is approximately 1:1 in some embodiments, although other ratios are also possible.
In other embodiments, either or both of the oxygen-lean second nitride layer 616b and the blocking dielectric 620 may include a high K dielectric. Suitable high K dielectrics include hafnium based materials such as HfSiON, HfSiO or HfO, Zirconium based material such as ZrSiON, ZrSiO or ZrO, and Yttrium based material such as Y2O3.
In another embodiment, shown in
Referring to
In accordance with the present disclosure, the non-planar multigate memory transistor 700 of
As with the embodiments described above, the high work function gate electrode 714 includes a doped polysilicon layer formed or deposited in a low pressure CVD process and having a thickness of from about 200 Å to about 2000 Å. The polysilicon layer of the high work function gate electrode 714 can be formed or grown directly as a doped polysilicon layer through the addition of gases such as phosphine, arsine, diborane or BF2, and is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 eV to about 5.3 eV. In an exemplary embodiment, the polysilicon layer of the high work function gate electrode 714 is doped to a concentration of from about 1e14 cm−2 to about 1e16 cm−2.
The multi-layer charge-trapping region 716a-716c includes at least one inner oxygen-rich first nitride layer 716a comprising nitride closer to the tunnel dielectric layer 718, and an outer oxygen-lean second nitride layer 716b overlying the oxygen-rich first nitride layer. Generally, the outer oxygen-lean second nitride layer 716b comprises a silicon-rich, oxygen-lean nitride layer and comprises a majority of a charge traps distributed in the multi-layer charge-trapping region, while the oxygen-rich first nitride layer 716a comprises an oxygen-rich nitride or silicon oxynitride, and is oxygen-rich relative to the outer oxygen-lean second nitride layer to reduce the number of charge traps therein.
In some embodiments, such as that shown, the multi-layer charge-trapping region 716 further includes at least one thin, intermediate or anti-tunneling layer 716c comprising a dielectric, such as an oxide, separating outer oxygen-lean second nitride layer 716b from the oxygen-rich first nitride layer 716a. The anti-tunneling layer 716c substantially reduces the probability of electron charge that accumulates at the boundaries of outer oxygen-lean second nitride layer 716b during programming from tunneling into the oxygen-rich first nitride layer 716a, resulting in lower leakage current.
As with the embodiment described above, either or both of the oxygen-rich first nitride layer 716a and the outer oxygen-lean second nitride layer 716b can comprise silicon nitride or silicon oxynitride, and can be formed, for example, by a CVD process including N2O/NH3 and DCS/NH3 gas mixtures in ratios and at flow rates tailored to provide a silicon-rich and oxygen-rich oxynitride layer. The second nitride layer of the multi-layer charge storing structure is then formed on the middle oxide layer. The outer oxygen-lean second nitride layer 716b has a stoichiometric composition of oxygen, nitrogen and/or silicon different from that of the oxygen-rich first nitride layer 716a, and may also be formed or deposited by a CVD process using a process gas including DCS/NH3 and N2O/NH3 gas mixtures in ratios and at flow rates tailored to provide a silicon-rich, oxygen-lean top nitride layer.
In those embodiments including an intermediate or anti-tunneling layer 716c comprising oxide, the anti-tunneling layer can be formed by oxidation of the oxygen-rich first nitride layer 716a, to a chosen depth using radical oxidation. Radical oxidation may be performed, for example, at a temperature of 1000-1100 degrees Celsius using a single wafer tool, or 800-900 degrees Celsius using a batch reactor tool. A mixture of H2 and O2 gasses may be employed at a pressure of 300-500 Tor for a batch process, or 10-15 Tor using a single vapor tool, for a time of 1-2 minutes using a single wafer tool, or 30 min-1 hour using a batch process.
Finally, in those embodiments in which the blocking dielectric 720 comprises oxide, the oxide may be formed or deposited by any suitable means. In one embodiment the oxide of blocking dielectric layer 720 is a high temperature oxide deposited in a HTO CVD process. Alternatively, the blocking dielectric layer 720 or blocking oxide layer may be thermally grown, however it will be appreciated that in this embodiment the thickness of the outer oxygen-lean second nitride layer 716b may need to be adjusted or increased as some of the top nitride will be effectively consumed or oxidized during the process of thermally growing the blocking oxide layer.
A suitable thickness for the oxygen-rich first nitride layer 716a may be from about 30 Å to about 80 Å (with some variance permitted, for example ±10 A), of which about 5-20 Å may be consumed by radical oxidation to form the anti-tunneling layer 716c. A suitable thickness for the outer oxygen-lean second nitride layer 716b may be at least 30 Å. In certain embodiments, the outer oxygen-lean second nitride layer 716b may be formed up to 70 Å thick, of which 30-70 Å may be consumed by radical oxidation to form the blocking dielectric layer 720. A ratio of thicknesses between the oxygen-rich first nitride layer 716a and the outer oxygen-lean second nitride layer 716b is approximately 1:1 in some embodiments, although other ratios are also possible.
In other embodiments, either or both of the outer oxygen-lean second nitride layer 716b and the blocking dielectric layer 720 may comprise a high K dielectric. Suitable high K dielectrics include hafnium based materials such as HfSiON, HfSiO or HfO, Zirconium based material such as ZrSiON, ZrSiO or ZrO, and Yttrium based material such as Y2O3.
In another embodiment, the memory transistor is or includes a non-planar device comprising a vertical nanowire channel region formed in or from a semiconducting material projecting above or from a number of conducting, semiconducting layers on a substrate. In one version of this embodiment, shown in cut-away in
As with the embodiments described above, the high work function gate electrode 814 includes a doped polysilicon layer formed or deposited in a low pressure CVD process and having a thickness of from about 200 Å to about 2000 Å. The polysilicon layer of the high work function gate electrode 814 can be formed or grown directly as a doped polysilicon layer through the addition of gases such as phosphine, arsine, diborane or BF2, and is doped to a concentration or dose selected so that the minimum energy needed to remove an electron from the gate electrode is from at least about 4.8 eV to about 5.3 eV. In an exemplary embodiment, the polysilicon layer of the high work function gate electrode 814 is doped to a concentration of from about 1e14 cm−2 to about 1e16 cm−2.
In some embodiments, such as that shown in
Either or both of the oxygen-rich first nitride layer 810a and the oxygen-lean second nitride layer 810b can comprise silicon nitride or silicon oxynitride, and can be formed, for example, by a CVD process including N2O/NH3 and DCS/NH3 gas mixtures in ratios and at flow rates tailored to provide a silicon-rich and oxygen-rich oxynitride layer.
Finally, either or both of the oxygen-lean second nitride layer 810b and the blocking dielectric layer 812 may comprise a high K dielectric, such as HfSiON, HfSiO, HfO, ZrSiON, ZrSiO, ZrO, or Y2O3.
A suitable thickness for the oxygen-rich first nitride layer 810a may be from about 30 Å to about 80 Å (with some variance permitted, for example ±10 A), of which about 5-20 Å may be consumed by radical oxidation to form the anti-tunneling layer 820. A suitable thickness for the oxygen-lean second nitride layer 810b may be at least 30 Å, and a suitable thickness for the blocking dielectric layer 812 may be from about 30-70 Å.
The memory transistor 800 of
Referring to
The first and second dielectric layers 902, 910, can be deposited by CVD, radical oxidation or be formed by oxidation of a portion of the underlying layer or substrate. Generally the thickness of the high work function gate electrode 908 is from about 40-50 Å, and the first and second dielectric layers 902, 910, from about 20-80 Å.
Referring to
Although not shown, it will be understood that as in the embodiments described above the charge-trapping region 916 can include a multi-layer charge-trapping region comprising at least one lower or oxygen-rich first nitride layer closer to the tunnel dielectric layer 914, and an upper or oxygen-lean second nitride layer overlying the oxygen-rich first nitride layer. Generally, the oxygen-lean second nitride layer comprises a silicon-rich, oxygen-lean nitride layer and comprises a majority of a charge traps distributed in the multi-layer charge-trapping region, while the oxygen-rich first nitride layer comprises an oxygen-rich nitride or silicon oxynitride, and is oxygen-rich relative to the oxygen-lean second nitride layer to reduce the number of charge traps therein. In some embodiments, the multi-layer charge-trapping region 916 further includes at least one thin, intermediate or anti-tunneling layer comprising a dielectric, such as an oxide, separating the oxygen-lean second nitride layer from the oxygen-rich first nitride layer.
Next, a second or channel region opening 920 is anisotropically etched through tunneling oxide 914, charge-trapping region 916, and blocking dielectric 918,
Referring to
Referring to
Referring to
Referring to
Next, a high work function gate electrode 1022 is deposited into the second opening 1012 and the surface of the upper dielectric layer 1002 planarized to yield the intermediate structure illustrated in
The foregoing description of specific embodiments and examples of the invention have been presented for the purpose of illustration and description, and although the invention has been described and illustrated by certain of the preceding examples, it is not to be construed as being limited thereby. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed, and many modifications, improvements and variations within the scope of the invention are possible in light of the above teaching. It is intended that the scope of the invention encompass the generic area as herein disclosed, and by the claims appended hereto and their equivalents. The scope of the present invention is defined by the claims, which includes known equivalents and unforeseeable equivalents at the time of filing of this application.
This application is a continuation of U.S. patent application Ser. No. 14/811,346, filed Jul. 28, 2015, which is a continuation of U.S. patent application Ser. No. 14/159,315, filed on Jan. 20, 2014, now U.S. Pat. No. 9,093,318, issued on Jul. 28, 2015 which is a continuation of U.S. patent application Ser. No. 13/539,466, filed on Jul. 1, 2012, now U.S. Pat. No. 8,633,537, issued on Jan. 21, 2014, which is a continuation-in-part of patent application Ser. No. 13/288,919, filed Nov. 3, 2011, now U.S. Pat. No. 8,859,374, issued on Oct. 14, 2014, which is a divisional of U.S. patent Ser. No. 12/152,518, filed May 13, 2008, now U.S. Pat. No. 8,063,434, issued Nov. 22, 2011, which claims the benefit of priority to U.S. Provisional Patent Application No. 60/940,160, filed May 25, 2007, all of which application are hereby incorporated by reference in their entirety.
Number | Name | Date | Kind |
---|---|---|---|
4257832 | Schwabe et al. | Mar 1981 | A |
4395438 | Chiang | Jul 1983 | A |
4490900 | Chiu | Jan 1985 | A |
4543707 | Ito et al. | Oct 1985 | A |
4667217 | Janning | May 1987 | A |
4843023 | Chiu et al. | Jun 1989 | A |
4870470 | Bass et al. | Sep 1989 | A |
5179038 | Kinney et al. | Jan 1993 | A |
5348903 | Pfiester et al. | Sep 1994 | A |
5404791 | Kervagoret | Apr 1995 | A |
5405791 | Ahmad et al. | Apr 1995 | A |
5408115 | Chang | Apr 1995 | A |
5464783 | Kim et al. | Nov 1995 | A |
5500816 | Kobayashi | Mar 1996 | A |
5543336 | Enami et al. | Aug 1996 | A |
5550078 | Sung | Aug 1996 | A |
5573963 | Sung | Nov 1996 | A |
5773343 | Lee et al. | Jun 1998 | A |
5793089 | Fulford et al. | Aug 1998 | A |
5817170 | Desu et al. | Oct 1998 | A |
5847411 | Morii | Dec 1998 | A |
5861347 | Maiti et al. | Jan 1999 | A |
5937323 | Orczyk et al. | Aug 1999 | A |
5939333 | Hurley et al. | Aug 1999 | A |
5972765 | Clark et al. | Oct 1999 | A |
5972804 | Tobin et al. | Oct 1999 | A |
6001713 | Ramsbey et al. | Dec 1999 | A |
6015739 | Gardner et al. | Jan 2000 | A |
6020606 | Liao | Feb 2000 | A |
6023093 | Gregor et al. | Feb 2000 | A |
6025267 | Pey et al. | Feb 2000 | A |
6074915 | Chen et al. | Jun 2000 | A |
6114734 | Eklund | Sep 2000 | A |
6127227 | Lin et al. | Oct 2000 | A |
6136654 | Kraft et al. | Oct 2000 | A |
6140187 | Debusk et al. | Oct 2000 | A |
6147014 | Lyding et al. | Nov 2000 | A |
6150286 | Sun et al. | Nov 2000 | A |
6153543 | Chesire et al. | Nov 2000 | A |
6157426 | Gu | Dec 2000 | A |
6162700 | Hwang et al. | Dec 2000 | A |
6174758 | Nachumovsky | Jan 2001 | B1 |
6174774 | Lee | Jan 2001 | B1 |
6214689 | Lim et al. | Apr 2001 | B1 |
6217658 | Orczyk et al. | Apr 2001 | B1 |
6218700 | Papadas | Apr 2001 | B1 |
6268299 | Jammy et al. | Jul 2001 | B1 |
6277683 | Pradeep et al. | Aug 2001 | B1 |
6287913 | Agnello et al. | Sep 2001 | B1 |
6297096 | Boaz | Oct 2001 | B1 |
6297173 | Tobin et al. | Oct 2001 | B1 |
6321134 | Henley et al. | Nov 2001 | B1 |
6335288 | Kwan et al. | Jan 2002 | B1 |
6348380 | Weimer et al. | Feb 2002 | B1 |
6365518 | Lee et al. | Apr 2002 | B1 |
6399484 | Yamasaki et al. | Jun 2002 | B1 |
6406960 | Hopper et al. | Jun 2002 | B1 |
6429081 | Doong et al. | Aug 2002 | B1 |
6433383 | Ramsbey et al. | Aug 2002 | B1 |
6440797 | Wu et al. | Aug 2002 | B1 |
6444521 | Chang et al. | Sep 2002 | B1 |
6445030 | Wu et al. | Sep 2002 | B1 |
6461899 | Kitakado et al. | Oct 2002 | B1 |
6462370 | Kuwazawa | Oct 2002 | B2 |
6468927 | Zhang et al. | Oct 2002 | B1 |
6469343 | Miura et al. | Oct 2002 | B1 |
6518113 | Buynoski | Feb 2003 | B1 |
6559026 | Rossman et al. | May 2003 | B1 |
6573149 | Kizilyalli et al. | Jun 2003 | B2 |
6586343 | Ho et al. | Jul 2003 | B1 |
6586349 | Jeon et al. | Jul 2003 | B1 |
6596590 | Miura et al. | Jul 2003 | B1 |
6599795 | Ogata | Jul 2003 | B2 |
6602771 | Inoue et al. | Aug 2003 | B2 |
6610614 | Niimi et al. | Aug 2003 | B2 |
6624090 | Yu et al. | Sep 2003 | B1 |
6661065 | Kunikiyo | Dec 2003 | B2 |
6670241 | Kamal et al. | Dec 2003 | B1 |
6677213 | Ramkumar et al. | Jan 2004 | B1 |
6709928 | Jenne et al. | Mar 2004 | B1 |
6713127 | Subramony et al. | Mar 2004 | B2 |
6717860 | Fujiwara | Apr 2004 | B1 |
6730566 | Niimi et al. | May 2004 | B2 |
6746968 | Tseng et al. | Jun 2004 | B1 |
6768160 | Li et al. | Jul 2004 | B1 |
6768856 | Akwani et al. | Jul 2004 | B2 |
6774433 | Lee et al. | Aug 2004 | B2 |
6787419 | Chen et al. | Sep 2004 | B2 |
6818558 | Rathor et al. | Nov 2004 | B1 |
6833582 | Mine et al. | Dec 2004 | B2 |
6835621 | Yoo et al. | Dec 2004 | B2 |
6884681 | Kamal et al. | Apr 2005 | B1 |
6903422 | Goda et al. | Jun 2005 | B2 |
6906390 | Nomoto et al. | Jun 2005 | B2 |
6912163 | Zheng et al. | Jun 2005 | B2 |
6913961 | Hwang | Jul 2005 | B2 |
6917072 | Noguchi et al. | Jul 2005 | B2 |
6946349 | Lee et al. | Sep 2005 | B1 |
6958511 | Halliyal et al. | Oct 2005 | B1 |
7012299 | Mahajani et al. | Mar 2006 | B2 |
7015100 | Lee et al. | Mar 2006 | B1 |
7018868 | Yang et al. | Mar 2006 | B1 |
7033890 | Shone | Apr 2006 | B2 |
7033957 | Shiraiwa et al. | Apr 2006 | B1 |
7042054 | Ramkumar et al. | May 2006 | B1 |
7045424 | Kim et al. | May 2006 | B2 |
7060594 | Wang | Jun 2006 | B2 |
7084032 | Crivelli et al. | Aug 2006 | B2 |
7098154 | Yoneda | Aug 2006 | B2 |
7112486 | Cho et al. | Sep 2006 | B2 |
7115469 | Halliyal et al. | Oct 2006 | B1 |
7172940 | Chen et al. | Feb 2007 | B1 |
7238990 | Burnett et al. | Jul 2007 | B2 |
7250654 | Chen et al. | Jul 2007 | B2 |
7253046 | Higashi et al. | Aug 2007 | B2 |
7262457 | Hsu et al. | Aug 2007 | B2 |
7279740 | Bhattacharyya et al. | Oct 2007 | B2 |
7301185 | Chen et al. | Nov 2007 | B2 |
7312496 | Hazama | Dec 2007 | B2 |
7315474 | Lue | Jan 2008 | B2 |
7323742 | Georgescu | Jan 2008 | B2 |
7338869 | Fukada et al. | Mar 2008 | B2 |
7365389 | Jeon et al. | Apr 2008 | B1 |
7372113 | Tanaka et al. | May 2008 | B2 |
7390718 | Roizin et al. | Jun 2008 | B2 |
7410857 | Higashi et al. | Aug 2008 | B2 |
7425491 | Forbes | Sep 2008 | B2 |
7450423 | Lai et al. | Nov 2008 | B2 |
7463530 | Lue et al. | Dec 2008 | B2 |
7479425 | Ang et al. | Jan 2009 | B2 |
7482236 | Lee et al. | Jan 2009 | B2 |
7521751 | Fujiwara | Apr 2009 | B2 |
7535053 | Yamazaki | May 2009 | B2 |
7544565 | Kwak et al. | Jun 2009 | B2 |
7576386 | Lue | Aug 2009 | B2 |
7588986 | Jung | Sep 2009 | B2 |
7601576 | Suzuki et al. | Oct 2009 | B2 |
7612403 | Bhattacharyya | Nov 2009 | B2 |
7636257 | Lue | Dec 2009 | B2 |
7642585 | Wang et al. | Jan 2010 | B2 |
7646041 | Chae et al. | Jan 2010 | B2 |
7646637 | Liao | Jan 2010 | B2 |
7670963 | Ramkumar et al. | Mar 2010 | B2 |
7688626 | Lue et al. | Mar 2010 | B2 |
7692246 | Dreeskornfeld et al. | Apr 2010 | B2 |
7713810 | Hagemeyer et al. | May 2010 | B2 |
7714379 | Lee | May 2010 | B2 |
7723789 | Lin et al. | May 2010 | B2 |
7737488 | Lai et al. | Jun 2010 | B2 |
7790516 | Willer et al. | Sep 2010 | B2 |
7879738 | Wang | Feb 2011 | B2 |
7910429 | Dong et al. | Mar 2011 | B2 |
7927951 | Kim et al. | Apr 2011 | B2 |
7948799 | Lue et al. | May 2011 | B2 |
7999295 | Lai et al. | Aug 2011 | B2 |
8008713 | Dobuzinsky et al. | Aug 2011 | B2 |
8063434 | Polishchuk et al. | Nov 2011 | B1 |
8067284 | Levy | Nov 2011 | B1 |
8071453 | Ramkumar et al. | Dec 2011 | B1 |
8093128 | Koutny et al. | Jan 2012 | B2 |
8143129 | Ramkumar et al. | Mar 2012 | B2 |
8163660 | Puchner et al. | Apr 2012 | B2 |
8222688 | Jenne et al. | Jul 2012 | B1 |
8264028 | Lue et al. | Sep 2012 | B2 |
8283261 | Ramkumar | Oct 2012 | B2 |
8315095 | Lue et al. | Nov 2012 | B2 |
8318608 | Ramkumar et al. | Nov 2012 | B2 |
8482052 | Lue et al. | Jul 2013 | B2 |
8633537 | Polishchuk et al. | Jan 2014 | B2 |
8643124 | Levy et al. | Feb 2014 | B2 |
8710578 | Jenne et al. | Apr 2014 | B2 |
8859374 | Polishchuk et al. | Oct 2014 | B1 |
8860122 | Polishchuk et al. | Oct 2014 | B1 |
8940645 | Ramkumar et al. | Jan 2015 | B2 |
8993453 | Ramkumar et al. | Mar 2015 | B1 |
9093318 | Polishchuk et al. | Jul 2015 | B2 |
9306025 | Polishchuk et al. | Apr 2016 | B2 |
9349824 | Levy et al. | May 2016 | B2 |
9355849 | Levy et al. | May 2016 | B1 |
9449831 | Levy et al. | Sep 2016 | B2 |
9502543 | Polishchuk et al. | Nov 2016 | B1 |
20010052615 | Fujiwara | Dec 2001 | A1 |
20020020890 | Willer | Feb 2002 | A1 |
20020048200 | Kuwazawa | Apr 2002 | A1 |
20020048893 | Kizilyalli et al. | Apr 2002 | A1 |
20020109138 | Forbes | Aug 2002 | A1 |
20020141237 | Goda et al. | Oct 2002 | A1 |
20020154878 | Akwani et al. | Oct 2002 | A1 |
20030030100 | Lee et al. | Feb 2003 | A1 |
20030122204 | Nomoto et al. | Jul 2003 | A1 |
20030123307 | Lee et al. | Jul 2003 | A1 |
20030124873 | Xing et al. | Jul 2003 | A1 |
20030169629 | Goebel et al. | Sep 2003 | A1 |
20030183869 | Crivelli et al. | Oct 2003 | A1 |
20030227049 | Sakakibara | Dec 2003 | A1 |
20040067619 | Niimi et al. | Apr 2004 | A1 |
20040071030 | Goda et al. | Apr 2004 | A1 |
20040094793 | Noguchi et al. | May 2004 | A1 |
20040104424 | Yamazaki | Jun 2004 | A1 |
20040129986 | Kobayashi et al. | Jul 2004 | A1 |
20040129988 | Rotondaro et al. | Jul 2004 | A1 |
20040173918 | Kamal et al. | Sep 2004 | A1 |
20040183091 | Hibino | Sep 2004 | A1 |
20040183122 | Mine et al. | Sep 2004 | A1 |
20040207002 | Ryu et al. | Oct 2004 | A1 |
20040227196 | Yoneda | Nov 2004 | A1 |
20040227198 | Mitani et al. | Nov 2004 | A1 |
20040251489 | Jeon et al. | Dec 2004 | A1 |
20050026637 | Fischer et al. | Feb 2005 | A1 |
20050056892 | Seliskar | Mar 2005 | A1 |
20050062098 | Mahajani et al. | Mar 2005 | A1 |
20050070126 | Senzaki | Mar 2005 | A1 |
20050079659 | Duan et al. | Apr 2005 | A1 |
20050093054 | Jung | May 2005 | A1 |
20050098839 | Lee et al. | May 2005 | A1 |
20050110064 | Duan et al. | May 2005 | A1 |
20050116279 | Koh | Jun 2005 | A1 |
20050141168 | Lee et al. | Jun 2005 | A1 |
20050186741 | Roizin et al. | Aug 2005 | A1 |
20050205920 | Jeon et al. | Sep 2005 | A1 |
20050224866 | Higashi et al. | Oct 2005 | A1 |
20050227501 | Tanabe et al. | Oct 2005 | A1 |
20050230766 | Nomoto et al. | Oct 2005 | A1 |
20050236679 | Hori et al. | Oct 2005 | A1 |
20050245034 | Fukuda et al. | Nov 2005 | A1 |
20050266637 | Wang | Dec 2005 | A1 |
20050275010 | Chen et al. | Dec 2005 | A1 |
20050275012 | Nara et al. | Dec 2005 | A1 |
20060008959 | Hagemeyer | Jan 2006 | A1 |
20060017092 | Dong et al. | Jan 2006 | A1 |
20060051880 | Doczy et al. | Mar 2006 | A1 |
20060065919 | Fujiwara | Mar 2006 | A1 |
20060081331 | Campian | Apr 2006 | A1 |
20060111805 | Yokoyama et al. | May 2006 | A1 |
20060113586 | Wang | Jun 2006 | A1 |
20060113627 | Chen et al. | Jun 2006 | A1 |
20060131636 | Jeon et al. | Jun 2006 | A1 |
20060160303 | Ang et al. | Jul 2006 | A1 |
20060192248 | Wang | Aug 2006 | A1 |
20060202261 | Lue et al. | Sep 2006 | A1 |
20060202263 | Lee | Sep 2006 | A1 |
20060220106 | Choi et al. | Oct 2006 | A1 |
20060226490 | Burnett et al. | Oct 2006 | A1 |
20060228841 | Kim et al. | Oct 2006 | A1 |
20060228899 | Nansei et al. | Oct 2006 | A1 |
20060228907 | Cheng et al. | Oct 2006 | A1 |
20060237803 | Zhu et al. | Oct 2006 | A1 |
20060261401 | Bhattacharyya | Nov 2006 | A1 |
20060281331 | Wang | Dec 2006 | A1 |
20060284236 | Bhattacharyya | Dec 2006 | A1 |
20070012988 | Bhattacharyya | Jan 2007 | A1 |
20070029625 | Lue | Feb 2007 | A1 |
20070031999 | Ho et al. | Feb 2007 | A1 |
20070048916 | Suzuki et al. | Mar 2007 | A1 |
20070049048 | Rauf et al. | Mar 2007 | A1 |
20070051306 | Ivanov et al. | Mar 2007 | A1 |
20070066087 | Jung | Mar 2007 | A1 |
20070121380 | Thomas | May 2007 | A1 |
20070200168 | Ozawa et al. | Aug 2007 | A1 |
20070210371 | Hisamoto et al. | Aug 2007 | A1 |
20070215940 | Ligon | Sep 2007 | A1 |
20070231991 | Willer et al. | Oct 2007 | A1 |
20070232007 | Forbes | Oct 2007 | A1 |
20070246753 | Chu et al. | Oct 2007 | A1 |
20070262451 | Rachmady et al. | Nov 2007 | A1 |
20070267687 | Lue | Nov 2007 | A1 |
20070268753 | Lue et al. | Nov 2007 | A1 |
20070272916 | Wang et al. | Nov 2007 | A1 |
20070272971 | Lee et al. | Nov 2007 | A1 |
20080009115 | Willer et al. | Jan 2008 | A1 |
20080029399 | Tomita et al. | Feb 2008 | A1 |
20080048237 | Iwata | Feb 2008 | A1 |
20080054346 | Saitoh et al. | Mar 2008 | A1 |
20080057644 | Kwak et al. | Mar 2008 | A1 |
20080087942 | Hsu et al. | Apr 2008 | A1 |
20080121932 | Ranade | May 2008 | A1 |
20080135946 | Yan | Jun 2008 | A1 |
20080146042 | Kostamo et al. | Jun 2008 | A1 |
20080150003 | Chen et al. | Jun 2008 | A1 |
20080175053 | Lue et al. | Jul 2008 | A1 |
20080237684 | Specht et al. | Oct 2008 | A1 |
20080237694 | Specht et al. | Oct 2008 | A1 |
20080258203 | Happ et al. | Oct 2008 | A1 |
20080272424 | Kim | Nov 2008 | A1 |
20080286927 | Kim et al. | Nov 2008 | A1 |
20080290398 | Polishchuk et al. | Nov 2008 | A1 |
20080290399 | Levy et al. | Nov 2008 | A1 |
20080290400 | Jenne et al. | Nov 2008 | A1 |
20080291726 | Lue et al. | Nov 2008 | A1 |
20080293207 | Koutny et al. | Nov 2008 | A1 |
20080293254 | Ramkumar et al. | Nov 2008 | A1 |
20080293255 | Ramkumar | Nov 2008 | A1 |
20080296664 | Ramkumar et al. | Dec 2008 | A1 |
20090011609 | Ramkumar et al. | Jan 2009 | A1 |
20090039414 | Lue et al. | Feb 2009 | A1 |
20090045452 | Lue et al. | Feb 2009 | A1 |
20090065849 | Noda | Mar 2009 | A1 |
20090152618 | Matsuo et al. | Jun 2009 | A1 |
20090152621 | Polishchuk et al. | Jun 2009 | A1 |
20090179253 | Levy et al. | Jul 2009 | A1 |
20090206385 | Kim et al. | Aug 2009 | A1 |
20090227116 | Joo et al. | Sep 2009 | A1 |
20090242969 | Tanaka | Oct 2009 | A1 |
20090294836 | Kiyotoshi | Dec 2009 | A1 |
20090294844 | Tanaka et al. | Dec 2009 | A1 |
20090302365 | Bhattacharyya | Dec 2009 | A1 |
20100006922 | Matsuoka et al. | Jan 2010 | A1 |
20100041222 | Puchner et al. | Feb 2010 | A1 |
20100096687 | Balseanu et al. | Apr 2010 | A1 |
20100117138 | Huerta et al. | May 2010 | A1 |
20100117139 | Lue | May 2010 | A1 |
20100155823 | Lue et al. | Jun 2010 | A1 |
20100178759 | Kim et al. | Jul 2010 | A1 |
20100252877 | Nakanishi et al. | Oct 2010 | A1 |
20100270609 | Olsen et al. | Oct 2010 | A1 |
20100283097 | Endoh et al. | Nov 2010 | A1 |
20100295118 | Bhattacharyya | Nov 2010 | A1 |
20110018053 | Lo et al. | Jan 2011 | A1 |
20110163371 | Song et al. | Jul 2011 | A1 |
20110237060 | Lee et al. | Sep 2011 | A1 |
20110248332 | Levy et al. | Oct 2011 | A1 |
20120007167 | Hung et al. | Jan 2012 | A1 |
20120068159 | Fujiki et al. | Mar 2012 | A1 |
20120068250 | Ino et al. | Mar 2012 | A1 |
20130175604 | Polishchuk et al. | Jul 2013 | A1 |
20130309826 | Ramkumar et al. | Nov 2013 | A1 |
20140264551 | Polishchuk et al. | Sep 2014 | A1 |
20160300724 | Levy et al. | Oct 2016 | A1 |
Number | Date | Country |
---|---|---|
1107254 | Aug 1995 | CN |
1801478 | Jul 2006 | CN |
1832201 | Sep 2006 | CN |
101517714 | Aug 2009 | CN |
101859702 | Oct 2010 | CN |
101558481 | May 2012 | CN |
104254921 | Dec 2014 | CN |
2005347679 | Dec 2005 | JP |
2007515060 | Jun 2007 | JP |
2007318112 | Dec 2007 | JP |
2009260070 | Nov 2009 | JP |
20040070669 | Aug 2004 | KR |
20060100092 | Sep 2006 | KR |
200703671 | Jan 2007 | TW |
200847343 | Dec 2008 | TW |
2007064048 | Jun 2007 | WO |
2008129478 | Oct 2008 | WO |
2011162725 | Dec 2011 | WO |
2013148112 | Oct 2013 | WO |
2013148343 | Oct 2013 | WO |
Entry |
---|
“3.3V 64K x 18 Synchronous QuadPort Static RAM,” Cypress Preliminary CY7C0430BV, Cypress Semiconductor Corporation, Mar. 27, 2001; 36 pages. |
Hua-Ching Chien, Chin-Hsing Kao, Jui-Wen Chang and Tzung-Kuen Tsai_Two-bit SONOS type Flash using a band engineering in the nitride layer_Dated Jun. 17, 2005_4 pages. |
Hung et al., High-performance gate-all-around polycrystalline silicon nanowire with silicon nanocrystals nonvolatile memory, Appl. Phys. Lett, 98 162108 (2011), pub date: Apr. 22, 2011. |
Krishnaswamy Ramkumar_Cypress SONOS Technology_Dated Jul. 6, 2011_9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,466 dated Nov. 13, 2013; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,466 dated Nov. 27, 2012; 8 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/620,071 dated Jan. 23, 2015; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/620,071 dated Oct. 27, 2014; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/159,315 dated Feb. 18, 2015; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/159,315 dated Mar. 23, 2015; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/307,858 dated Nov. 27, 2015; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/811,346 dated Jul. 19, 2016; 7 pages. |
USPTO Requirement for Restriction for U.S. Appl. No. 12/152,518 dated Jun. 9, 2010; 5 pages. |
USPTO Requirement for Restriction for U.S. Appl. No. 14/307,858 dated May 18, 2015; 7 pages. |
“MAX 9000 Programmable Logic Device Family,” Altera, Jul. 1999, Version 6.01, pp. 1-40; 41 pages. |
L. Richard Carley, “Trimming Analog Circuits Using Floating-Gate Analog MOS Memory,” IEEE Journal of Solid-State circuits, vol. 24, No. 6, Dec. 1989, pp. 1569-1575; 7 pages. |
“1.8V, 500-MHz, 10-Output JEDEC-Compliant Zero Delay Buffer,” Cypress Advance Information, Feb. 12, 2004; 9 pages. |
“10 Gigabit Ethernet Technology Overview White Paper”, Revision 1.0, Retrieved from Internet: URL: http://www.10gea.org, May 2001. |
“16K x 8/9 Dual-Port Static RAM with Sem, Int, Busy,” Cypress Semiconductor Data Book, May 1995, CY7C006 and CY7C016, pp. 6:1-17; 10 pages. |
“1K x 8 Dual-Port Static RAM,” Cypress Semiconductor Data Book, May 1995, CY7C130/CY7C131 and CY7C140/CY7C141, pp. 6:37-49; 8 pages. |
“1kHz to 30MHz Resistor Set SOT-23 Oscillator”, Initial Release Final Electrical Specifications LTC1799, Linear Technology Corporation, Jan. 2001, pp. 1-4. |
“200-MBaud HOTLink Transceiver,” Cypress Semiconductor Corporation, Revised Feb. 13, 2004, CY7C924ADX, Document #38-02008 Rev. *D; 62 pages. |
“2K x 16 Dual-Port Static Ram,” Cypress Semiconductor Data Book, May 1995, CY7C133 and CY7C143, pp. 6:63-73; 7 pages. |
“2K x 8 Dual-Port Static RAM,” Cypress Semiconductor Data Book, May 1995, CY7C132/CY7C136 and CY7C142/CY7C146, pp. 6:50-62; 8 pages. |
“A Novel Integration Technology of EEPROM Embedded CMOS Logic VLSI Suitable for ASIC Applications”, by Masataka Takebuchi et al., IEEE 1992 Custom Integrated Circuits Conference, pp. 9.6.1-9.6.4. |
“A Novel Robust and Low Cost Stack Chips Package and Its Thermal Performance”, by Soon-Jin Cho et al., IEEE Transaction on Advanced Packaging, vol. 23, No. 2, May 2000, pp. 257-265. |
“A Planar Type EEPROM Cell Structure by Standard CMOS Process for Integration with Gate Array, Standard Cell, Microprocessor and for Neural Chips”, by Katsuhiko Ohsaki et al., IEEE 1993 Custom Integrated Circuits Conference, pp-23.6.1-23.6A. |
“A Single Chip Sensor & Image Processor for Fingerprint Verification” Anderson, S., et al., IEEE Custom Integrated Circuits Conference, May 12-15, 1991. |
“A Single Poly EPROM for Custom CMOS Logic Applications”, by Reza Kazerounian et al., IEEE 1986 Custom Integrated Circuits Conference, pp. 59-62. |
“A Wide-Bandwidth Low-Voltage PLL for PowerPC.TM. Microprocessors”, by Jose Alvarez et al., IEEE Journal of Solid-State Circuits, vol. 30, No. 4, Apr. 1995, pp. 383-391. |
“About SMaL Camera Technologies, Inc.”, SMaL Camera Technologies, 2001, 1 page. |
“Achieving Uniform nMOS Device Power Distribution for Sub-micron ESD Reliability;” Charvaka Duwuy, Carlos Diaz, and Tim Haddock; 1992; 92-131 through 92-134, no month. |
“ADNS-2030 High Performance, Low Power Optical Mouse Sensor (Optimized for Cordless Mouse Applications),” Agilent Technologies, downloaded Oct. 10, 2005, <http://www.home.agilent.com/USeng/nav/-536893734,536883737/pd.html>; 2 pages. |
“ADNS-2051 High-Performance Optical Mouse Sensor,” Agilent Technologies, downloaded Oct. 10, 2005, <http://www.home.agilent.com/USeng/nav/-536893734,536883737/pd.html>; 2 pages. |
“Agilent ADNK-2030 Solid-State Optical Mouse Sensor,” Agilent Technologies Inc., Sample Kit, 2003; 1 page. |
“Agilent ADNS-2030 Low Power Optical Mouse Sensor,” Agilent Technologies Inc., Data Sheet, 2005; 34 pages. |
“Agilent ADNS-2051 Optical Mouse Sensor,” Agilent Technologies Inc., Product Overview, 2003; 2 pages. |
“Agilent Optical Mouse Sensors,” Agilent Technologies Inc., Selection Guide, 2004; 3 pages. |
“Algorithm for Managing Multiple First-In, First-Out Queues from a Single Shared Random-Access Memory,” IBM Technical Disclosure Bulletin, Aug. 1989; 5 pages. |
“Am99C10A 256.times.48 Content Addressable Memory”, Advanced Micro Devices, Dec. 1992. |
“An Analog PPL-Based Clock and Data Recovery Circuit with High Input Jitter Tolerance;” Sun, Reprinted from IEEE Journal of Solid-State Circuits, 1989; 4 pages. |
“An EEPROM for Microprocessors and Custom Logic”, by Roger Cuppens et al., IEEE Journal of Solid-State Circuits, vol. SC-20, No. 2, Apr. 1985, pp. 603-608. |
“An EPROM Cell Structure foe EPLDs Compatible with Single Poly Gate Process”, by Kuniyushi Yoshikawa et al., Extended Abstracts of the 18th (1986 International) Conference on Solid State Devices and Materials, Tokyo, 1986, pp. 323-326. |
“An Experimental 5-V-Only 256-kbit CMOS EEPROM with a High-Performance Single-Polysilicon Cell”, by Jun-Ichi Vliyamoto et al., IEEE Journal of Solid State Circuits, vol. SC-21, No. 5, Oct. 1986, pp. 852-860. |
Chen et al., “Performance Improvement of SONOS Memory by Bandgap Engineering of Charge-Trapping Layer,” IEEE Electron Device Letters, Apr. 2004, vol. 25, No. 4, pp. 205-207; 3 pages. |
European Search Report for European Application No. 13767422.2 dated Mar. 30, 2017; 6 pages. |
European Search Report for European Application No. 13767422.2 dated Oct. 20, 2015; 5 pages. |
International Search Report for International Application No. PCT/US08/06627 dated Aug. 26, 2008; 2 pages. |
International Search Report for International Application No. PCT/US12/021583 dated May 8, 2012; 2 pages. |
International Search Report for International Application No. PCT/US13/32339 dated May 30, 2013; 2 pages. |
International Search Report for International Application No. PCT/US13/48876 dated Jul. 26, 2013; 5 pages. |
International Search Report for International Application No. PCT/US13/48885 dated Nov. 14, 2013; 2 pages. |
Lue et al., “BE-SONOS: A Bandgap Engineered SONOS with Excellent Performance and Reliability,” IEEE, 2005; 4 pages. |
Lue, Hang-Ting et al., “Reliability Model of Bandgap Engineered SONOS (be-SONOS)”, IEEE, 2006, 4 pgs. |
Milton Ohring, “The Materials Science of Thin Films: Deposition and Structure,” 2nd Edition, Academic Press, 2002, pp. 336-337; 4 pages. |
SIPO Office Action for Application No. 201380031840.8 dated Jan. 6, 2017; 8 pages. |
Wang, Szu-Yu et al., “Reliability and processing effects of bandgap engineered SONOS flash memory”, 2007 IEEE, International Reliability Symposium, Apr. 18, 2007, 5 pgs. |
Written Opinion of the International Searching Authority for International Application No. PCT/US08/06627 dated Aug. 26, 2008; 5 pages. |
Written Opinion of the International Searching Authority for International Application No. PCT/US13/32339 dated May 30, 2013; 7 pages. |
Written Opinion of the International Searching Authority for International Application No. PCT/US13/48876 dated Jul. 26, 2013; 3 pages. |
Written Opinion of the International Searching Authority for International Application No. PCT/US2012/21583 dated May 8, 2012; 4 pages. |
Written Opinion of the International Searching Authority for International Application No. PCT/US2013/048885 dated Nov. 14, 2013; 7 pages. |
Wu et al., “SONOS Device with Tapered Bandgap Nitride Layer,” IEEE Transactions on Electron Devices, May 2005, vol. 52, No. 5, pp. 987-992; 6 pages. |
Yang et al., “Reliability considerations in scaled SONOS nonvolatile memory devices, solid state Electronics”, 43(1999)2025-2032. |
Chinese Office Action for Application No. 200880000820.3 dated Jan. 26, 2011; 6 pages. |
SIPO Office Action for CN Application No. 201380031969.9 dated Aug. 19, 2016; 8 pages. |
USPTO Advisory Action for U.S. Appl. No. 12/197,466 dated Jan. 31, 2012; 3 pages. |
USPTO Advisory Action for U.S. Appl. No. 14/605,231 dated Mar. 9, 2016; 3 pages. |
USPTO Advisory Action for U.S. Appl. No. 14/605,231 dated Jul. 5, 2016; 3 pages. |
USPTO Final Rejection for U.S. Appl. No. 12/124,855 dated Jan. 31, 2012; 7 pages. |
USPTO Final Rejection for U.S. Appl. No. 12/124,855 dated May 10, 2010; 11 pages. |
USPTO Final Rejection for U.S. Appl. No. 12/197,466 dated Nov. 17, 2011; 13 pages. |
USPTO Final Rejection for U.S. Appl. No. 14/307,858 dated Oct. 8, 2015; 6 pages. |
USPTO Final Rejection for U.S. Appl. No. 14/605,231 dated Dec. 17, 2015; 15 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 13/539,458 dated Mar. 13, 2013; 5 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 13/539,458 dated Oct. 2, 2014; 5 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 13/620,071 dated Apr. 3, 2014; 12 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 13/620,071 dated Jul. 18, 2014; 5 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/124,855 dated Jan. 18, 2011; 5 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/124,855 dated Aug. 16, 2011; 9 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/124,855 dated Oct. 29, 2009; 9 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/152,518 dated Mar. 9, 2011; 4 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/152,518 dated Sep. 29, 2010; 5 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 12/197,466 dated Jun. 1, 2011; 11 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 13/288,919 dated Jun. 19, 2014; 5 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 13/288,919 dated Dec. 5, 2013; 4 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 13/539,466 dated Sep. 28, 2012; 9 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 14/159,315 dated Oct. 21, 2014; 12 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 14/307/858 dated Jun. 29, 2015; 5 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 14/605,231 dated Jul. 7, 2015; 13 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/124,855 dated May 1, 2012; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/124,855 dated May 3, 2011; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/124,855 dated Jul. 28, 2010; 6 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/124,855 dated Aug. 1, 2012; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/152,518 dated Jul. 14, 2011; 6 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/197,466 dated Jun. 15, 2012; 4 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 12/197,466 dated Sep. 24, 2012; 8 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/288,919 dated Apr. 28, 2014; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/288,919 dated Jul. 8, 2014; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/288,919 dated Aug. 26, 2014; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,458 dated May 24, 2013; 8 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,458 dated Aug. 4, 2014; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,458 dated Nov. 3, 2014; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/539,466 dated Sep. 4, 2013; 9 pages. |
Japanese Office Action for Japanese Application No. 2013-549612 dated Aug. 4, 2015; 8 pages. |
Japanese Office Action for Japanese Application No. 2015-503338 dated Feb. 21, 2017; 21 pages. |
SIPO Office Action for Application No. 200910134374.1 dated Jan. 21, 2015; 5 pages. |
SIPO Office Action for Application No. 200910134374.1 dated Feb. 3, 2016; 2 pages. |
SIPO Office Action for Application No. 200910134374.1 dated Jul. 29, 2014; 5 pages. |
SIPO Office Action for Application No. 200910134374.1 dated Jul. 30, 2015; 2 pages. |
SIPO Office Action for Application No. 200910134374.1 dated Sep. 22, 2013; 4 pages. |
SIPO Office Action for Application No. 20120000107.5 dated Apr. 1, 2015; 5 pages. |
SIPO Office Action for Application No. 20120000107.5 dated May 12, 2016; 5 pages. |
SIPO Office Action for Application No. 20120000107.5 dated Jul. 25, 2014; 4 pages. |
SIPO Office Action for Application No. 20120000107.5 dated Oct. 9, 2015; 2 pages. |
SIPO Office Action for Application No. 201280000107.5 dated Nov. 29, 2016; 5 pages. |
SIPO Office Action for Application No. 2013800168932 dated Sep. 1, 2016; 7 pages. |
TIPO Office Action for Application No. 102110223 dated Nov. 18, 2016; 10 pages. |
TIPO Office Action for Taiwan Application No. 101101220 dated Oct. 15, 2015; 4 pages. |
USPTO Advisory Action for U.S. Appl. No. 11/811,958 dated Mar. 16, 2010; 4 pages. |
USPTO Advisory Action for U.S. Appl. No. 11/811,958 dated Apr. 20, 2010; 6 pages. |
USPTO Advisory Action for U.S. Appl. No. 11/811,958 dated May 14, 2013; 4 pages. |
USPTO Advisory Action for U.S. Appl. No. 11/811,958 dated Jun. 2, 2011; 5 pages. |
USPTO Advisory Action for U.S. Appl. No. 13/436,872 dated Aug. 4, 2015; 2 pages. |
USPTO Final Rejection for U.S. Appl. No. 11/811,958 dated Jan. 6, 2010; 17 pages. |
USPTO Final Rejection for U.S. Appl. No. 11/811,958 Dated Mar. 13, 2013; 22 pages. |
USPTO Final Rejection for U.S. Appl. No. 11/811,958 dated Mar. 15, 2011; 13 pages. |
USPTO Final Rejection for U.S. Appl. No. 13/007,533 dated Sep. 24, 2012; 13 pages. |
USPTO Final Rejection for U.S. Appl. No. 13/436,872 dated May 27, 2015; 14 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 11/811,958 dated Dec. 7, 2011; 13 pages. |
USPTO Non Final Rejection for U.S. Appl. No. 13/007,533 dated Apr. 12, 2012; 9 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 11/811,958 dated May 13, 2009; 14 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 11/811,958 dated Oct. 1, 2012; 17 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 11/811,958 dated Oct. 7, 2010; 12 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 13/436,872 dated Dec. 19, 2014; 15 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 13/917,500 dated Jan. 5, 2015; 13 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 14/172,775 dated Jun. 22, 2015; 14 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/007,533 dated Mar. 7, 2013; 8 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/007,533 dated Jun. 18, 2013; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/007,533 dated Sep. 6, 2013; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/007,533 dated Nov. 27, 2012; 13 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/007,533 dated Dec. 6, 2013; 10 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/436,872 dated Jan. 15, 2016; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/436,872 dated Sep. 15, 2015; 9 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/917,500 dated Jun. 1, 2015; 6 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/917,500 dated Sep. 14, 2015; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/917,500 dated Dec. 31, 2015; 5 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/172,775 dated Sep. 4, 2015; 7 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/172,775 dated Dec. 18, 2015; 6 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/436,872 dated May 11, 2016; 5 pages. |
USPTO Requirement for Restriction for U.S. Appl. No. 13/007,533 dated Dec. 6, 2011; 7 pages. |
USPTO Requirement Restriction for U.S. Appl. No. 12/197,466 dated Mar. 11, 2011; 5 pages. |
SIPO Office Action for Chinese Application No. 2013800319699 dated May 31, 2017; 11 pages. |
TIPO Office Action for Taiwan Application No. 106107213 dated Jul. 4, 2017; 6 pages. |
SIPO Office Action for International Application No. 2013800168932 dated Apr. 21, 2017; 7 pages. |
USPTO Final Rejection for U.S. Appl. No. 14/605,231 dated Jul. 10, 2017; 7 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 15/376,282 dated Jul. 11, 2017; 16 pages. |
SIPO Office Action for Application No. 20120000107.5 dated Sep. 20, 2017; 6 pages. |
SIPO Office Action for Application No. 201380031840.8 dated Sep. 25, 2017; 6 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 15/099,025 dated Oct. 6, 2017; 11 pages. |
USPTO Non-Final Rejection for U.S. Appl. No. 15/189,668 dated Sep. 22, 2017; 11 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 14/605,231 dated Oct. 18, 2017; 8 pages. |
Japanese Office Action for Japanese Application No. 2015-503338 dated Dec. 5, 2017; 5 pages. |
USPTO Final Rejection for U.S. Appl. No. 15/376,282 dated Dec. 19, 2017; 19 pages. |
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20170092729 A1 | Mar 2017 | US |
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60940160 | May 2007 | US |
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