Memory transistor with multiple charge storing layers and a high work function gate electrode

Information

  • Patent Grant
  • 11721733
  • Patent Number
    11,721,733
  • Date Filed
    Friday, July 2, 2021
    2 years ago
  • Date Issued
    Tuesday, August 8, 2023
    9 months ago
Abstract
Semiconductor devices including non-volatile memory transistors and methods of fabricating the same to improve performance thereof are provided. In one embodiment, the memory transistor comprises an oxide-nitride-oxide (ONO) stack on a surface of a semiconductor substrate, and a high work function gate electrode formed over a surface of the ONO stack. Preferably, the gate electrode comprises a doped polysilicon layer, and the ONO stack comprises multi-layer charge storing layer including at least a substantially trap free bottom oxynitride layer and a charge trapping top oxynitride layer. More preferably, the device also includes a metal oxide semiconductor (MOS) logic transistor formed on the same substrate, the logic transistor including a gate oxide and a high work function gate electrode. In certain embodiments, the dopant is a P+ dopant and the memory transistor comprises N-type (NMOS) silicon-oxide-nitride-oxide-silicon (SONOS) transistor while the logic transistor a P-type (PMOS) transistor. Other embodiments are also disclosed.
Description
TECHNICAL FIELD

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.


BACKGROUND OF THE INVENTION

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 FIG. 1A, if the charge trapping layer is silicon (Si) rich there is a large, initial window or difference between VTP, represented by graph or line 102, and the VTE, represented by line 104, but the window collapse very rapidly in retention mode to an end of life (EOL 106) of less than about 1.E+07 seconds.


Referring to FIG. 1B, if on the other hand the charge trapping layer is if a high quality nitride layer, that is one having a low stoichiometric concentration of Si, the rate of collapse of the window or Vt slope in retention mode is reduced, but the initial program-erase window is also reduced. Moreover, the slope of Vt in retention mode is still appreciably steep and the leakage path is not sufficiently minimized to significantly improve data retention, thus EOL 106 is only moderately improved.


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.


SUMMARY OF THE INVENTION

The present invention provides a solution to these and other problems, and offers further advantages over conventional memory transistors or devices and methods of forming the same.


In a first aspect, the present invention is directed to a non-volatile memory transistor including: (i) an oxide-nitride-oxide (ONO) dielectric stack on a surface of a semiconductor substrate; and (ii) high work function gate electrode formed over a surface of the ONO dielectric stack. Preferably, the high work function gate electrode comprises a doped polycrystalline silicon or polysilicon (poly) layer. More preferably, the doped polysilicon layer comprises a P+ dopant, such as boron or difluoroborane (BF2), and the substrate comprises a silicon surface on which the ONO dielectric stack is formed to form a silicon-oxide-nitride-oxide-silicon (SONOS) gate stack of a NMOS SONOS memory transistor.


In certain embodiments, the ONO dielectric stack comprises a multi-layer charge storage layer including at least a substantially trap free bottom oxynitride layer and a charge trapping top oxynitride layer. In one version of these embodiments, for example, the top oxynitride layer is formed under conditions selected to form a silicon-rich, oxygen-lean oxynitride layer, and the bottom oxynitride layer is formed under conditions selected to form a silicon-rich, oxygen-rich oxynitride layer.


In another aspect, the present invention is directed to a semiconductor device including both a non-volatile memory transistor and a metal oxide semiconductor (MOS) logic transistor and methods of forming the same. The memory transistor includes an ONO dielectric stack including a multi-layer charge storage layer formed on a surface of a semiconductor substrate, and a high work function gate electrode formed over a surface of the ONO dielectric stack. Preferably, the high work function gate electrode of the memory transistor comprises a doped polysilicon layer. More preferably, the MOS logic transistor also includes a high work function gate electrode formed over a gate oxide on the surface of the substrate.


In one embodiment, the high work function gate electrodes of the memory transistor and the MOS logic transistor comprise a P+ doped polysilicon layer deposited over the ONO stack and gate oxide on a silicon substrate to form an NMOS SONOS memory transistor and a P-type (PMOS) logic transistor. The multi-layer charge storing layer can include, for example, a substantially trap free bottom oxynitride layer and a charge trapping top oxynitride layer.


In one embodiment, a method of forming such a semiconductor device comprises steps of: (i) forming an ONO dielectric stack on a surface of a semiconductor substrate in at least a first region in which a non-volatile memory transistor is to be formed, the ONO dielectric stack including a multi-layer charge storage layer; (ii) forming an oxide layer on the surface of the substrate in a second region in which a MOS logic transistor is to be formed; and (iii) forming a high work function gate electrode on a surface of the ONO dielectric stack. Preferably, the step of forming a high work function gate electrode on a surface of the ONO dielectric stack comprises the step of forming a doped polysilicon layer on a surface of the ONO dielectric stack. More preferably, the step of forming a doped polysilicon layer on a surface of the ONO dielectric stack further comprises the step of also forming the doped polysilicon layer on a surface of the oxide layer of the MOS logic transistor form a high work function gate electrode thereon.


In certain embodiments, the semiconductor substrate includes a silicon surface over which the ONO dielectric stack is formed, and the step of forming a doped polysilicon layer comprises the step of forming a P+ doped polysilicon layer to form an NMOS SONOS memory transistor and a PMOS logic transistor. Generally, the polysilicon layer can be doped by ion implantation with boron or BF2, before or after patterning the polysilicon layer, the ONO dielectric stack and the oxide layer to form gate stacks of the memory transistor and the MOS logic transistor.


In other embodiments, the step of forming the ONO dielectric stack comprises the step of forming a multi-layer charge storage layer overlying a lower or tunnel oxide layer on the surface of the substrate, followed depositing or growing an upper or blocking oxide layer over the multi-layer charge storage layer. Preferably, the step of forming the multi-layer charge storage layer comprises the step of forming a substantially trap free bottom oxynitride layer followed by forming a charge trapping top oxynitride layer overlying the trap free bottom oxynitride layer. More preferably, the bottom oxynitride layer is formed under conditions selected to form a silicon-rich, oxygen-rich oxynitride layer, and the top oxynitride layer is formed under conditions selected to form a silicon-rich, oxygen-lean oxynitride layer. Optionally, the charge trapping top oxynitride layer formed, for example, in a chemical vapor deposition (CVD) process using a process gas comprising Bis-TertiaryButylAminoSilane (BTBAS) selected to increase a concentration of carbon and thereby the number of traps therein.





BRIEF DESCRIPTION OF THE DRAWINGS

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:



FIG. 1A is a graph showing data retention for a memory transistor using a charge storage layer formed according to a conventional method and having a large initial difference between programming and erase voltages but which loses charge quickly;



FIG. 1B is a graph showing data retention for a memory transistor using a charge storage layer formed according to a conventional method and having a smaller initial difference between programming and erase voltages;



FIGS. 2A through 2D are partial cross-sectional side views of a semiconductor device illustrating a process flow for forming a semiconductor device including a logic transistor and non-volatile memory transistor according to an embodiment of the present invention; and



FIG. 3 is a partial cross-sectional side view of a semiconductor device including a logic transistor and non-volatile memory transistor comprising high work function gate electrodes according to an embodiment of the present invention.





DETAILED DESCRIPTION

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 FIGS. 2A through 2D, which are partial cross-sectional side views of intermediate structures illustrating a process flow for forming a semiconductor device including both memory and logic transistors. For purposes of clarity, many of the details of semiconductor fabrication that are widely known and are not relevant to the present invention have been omitted from the following description.


Referring to FIG. 2, fabrication of the semiconductor device begins with formation of an ONO dielectric stack 202 over a surface 204 of a wafer or substrate 206. Generally, the ONO dielectric stack 202 includes a thin, lower oxide layer or tunneling oxide layer 208 that separates or electrically isolates a charge trapping or storage layer 210 from a channel region (not shown) of the memory transistor in the substrate 206, and a top or blocking oxide layer 212. Preferably, as noted above and as shown in FIGS. 2A-2D, the charge storage layer 210 is a multi-layer charge storage layer including at least a top, charge trapping oxynitride layer 210A and a lower, substantially trap free oxynitride layer 210B.


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 oxide 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 308 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 FIG. 2B, in those embodiments in which the semiconductor device is to further include a logic transistor, such as a MOS logic transistor, formed on the surface of the same substrate the ONO dielectric stack 202 is removed from a region or area of the surface 204 in which the logic transistor is to be formed, and an oxide layer 214 the formed thereon.


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 FIG. 2C, forming of the doped polysilicon layer begins with the deposition of a conformal polysilicon layer 216 having a thickness of from about 200 Å to about 2000 Å over the ONO dielectric stack 202 and the oxide layer 214. The polysilicon layer 216 can be formed or deposited by any suitable means including, for example, deposition in a low pressure CVD process using a silicon source or precursor. In one embodiment the polysilicon layer 216 is deposited in a low pressure CVD process using a silicon containing process gas, such as silane or dichlorosilane, and N2, while maintaining the substrate 206 in a chamber at a pressure of from about 5 to 500 mT, and at a temperature of from about 600° C. to about 1000° C. for a period of from about 20 minutes to about 100 minutes to a substantially undoped polysilicon layer. The polysilicon layer 216 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.


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 FIG. 2D, the polysilicon layer 216 and the underlying dielectric stack 202 and oxide layer 214 are patterned or etched to form high work function gate electrodes 218 of the memory transistor 220 and logic transistor 222. In one embodiment polysilicon layer 216 can be etched or patterned using a plasma comprising hydrobromic acid (HBr), chlorine (CL2) and/or oxygen (O2) at a pressure of about 25 mTorr, and a power of about 450 W. The oxide layers 208, 212, 214, and oxynitride layers 210A, 210B, can be etched using standard photolithographic and oxide etch techniques as described. For example, in one embodiment the patterned polysilicon layer 216 is used as a mask, and the exposed oxide layers 208, 212, 214, and oxynitride layers 210A, 210B, etched or removed using low pressure RF plasma. Generally, the plasma is formed from a processing gas comprising a fluorinated hydrocarbon and/or fluorinated carbon compounds, and further including Ar and N2 at flow rates selected to maintain a pressure in the etch chamber of from about 50 mT to about 250 mT during processing.


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 FIG. 3. Referring to FIG. 3, the memory transistor 304 is formed on a silicon substrate 306 and comprises a high work function gate electrode 308 formed from a doped polysilicon layer overlying a dielectric stack 310. The dielectric stack 310 overlies and controls current through a channel region 312 separating heavily doped source and drain (S/D) regions 314. Preferably, the dielectric stack 310 includes a tunnel oxide 316, a multi-layer charge storage layer 318A, 318B, and a top or blocking oxide layer 320. More preferably, the multi-layer charge storage layer 318A, 318B, includes at least a top, charge trapping oxynitride layer 318A and a lower, substantially trap free oxynitride layer 318B. Optionally, as shown in FIG. 3, the memory transistor 304 further includes one or more sidewall spacers 322 surrounding the gate stack to electrically insulate it from contacts (not shown) to the S/D regions 320 and from other transistors in the semiconductor device formed on the substrate 306.


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 FIG. 3, the gate electrode 324 of the logic transistor 302 also comprises a high work function gate electrode formed from a doped polysilicon layer.


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.


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.

Claims
  • 1. A semiconductor memory device comprising: a semiconductor substrate;an oxide-nitride-oxide structure formed over the substrate, the oxide-nitride-oxide structure having a tunnel oxide layer, a blocking oxide layer and a multi-layer charge storing layer formed between the tunnel oxide layer and the blocking oxide layer;the multi-layer charge storing layer including a first layer and a second layer, the first layer being an oxygen-rich oxynitride layer and the second layer being an oxygen-lean oxynitride layer; anda gate coupled to the oxide-nitride-oxide structure.
  • 2. The semiconductor memory device of claim 1, wherein the first layer of the multi-layer charge storing layer is formed closer to the tunnel oxide layer and further from the blocking oxide layer.
  • 3. The semiconductor memory device of claim 2, wherein the second layer of the multi-layer charge storing layer is formed closer to the blocking oxide layer and further from the tunnel oxide layer.
  • 4. The semiconductor memory device of claim 2, wherein the tunneling oxide layer is between the substrate and the first layer and wherein the blocking oxide layer is between the second layer and the gate.
  • 5. A semiconductor device comprising: a semiconductor substrate;a non-volatile memory transistor including an oxide-nitride-oxide structure, the oxide-nitride-oxide structure having a tunnel oxide layer, a blocking oxide layer and a multi-layer charge storing layer formed between the tunnel oxide layer and the blocking oxide layer, wherein the multi-layer charge storing layer includes a first layer and a second layer, the first layer being an oxygen-rich oxynitride layer and the second layer being an oxygen-lean oxynitride layer; anda logic transistor having a gate oxide and a high work function gate electrode.
  • 6. The semiconductor device of claim 5, further comprising an isolation structure between the non-volatile memory transistor and the logic transistor.
  • 7. The semiconductor device of claim 5, further comprising a gate coupled to the oxide-nitride-oxide structure.
  • 8. The semiconductor device of claim 7, wherein the blocking oxide layer is formed between the gate and the multi-layer charge storing layer.
  • 9. The semiconductor device of claim 5, wherein the first layer of the multi-layer charge storing layer is formed closer to the tunnel oxide layer and further from the blocking oxide layer.
  • 10. The semiconductor device of claim 9, wherein the second layer of the multi-layer charge storing layer is formed closer to the blocking oxide layer and further from the tunnel oxide layer.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of and claims the benefit of priority under 35 U.S.C. 119(e) to U.S. patent application Ser. No. 16/600,768, filed Oct. 14, 2019, which is a continuation of U.S. patent application Ser. No. 15/376,282, filed Dec. 12, 2016, now U.S. Pat. No. 10,446,656, issued Oct. 15, 2019, which is a continuation of U.S. Non-Provisional application Ser. No. 15/335,180, filed on Oct. 26, 2016, now U.S. Pat. No. 9,929,240, issued Mar. 27, 2018, which is a continuation of U.S. patent application Ser. No. 14/811,346, filed Jul. 28, 2015, now U.S. Pat. No. 9,502,543, issued on Nov. 22, 2016, 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 are hereby incorporated by reference in their entirety.

US Referenced Citations (354)
Number Name Date Kind
4257832 Schwab 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, Jr. et al. Sep 1989 A
5179038 Kinney Jan 1993 A
5348903 Pfiester et al. Feb 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, Jr. 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 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 Nov 2004 B1
6833582 Mine et al. Dec 2004 B2
6835621 Yoo et al. Dec 2004 B2
6867118 Noro Mar 2005 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
7189606 Wang Mar 2007 B2
7230294 Lee Jun 2007 B2
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 et al. 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
7811890 Hsu et al. Oct 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
7972930 Jang et al. Jul 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
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
9929240 Polishchuk et al. Mar 2018 B2
10304968 Ramkumar et al. May 2019 B2
10593812 Ramkumar et al. Mar 2020 B2
20010052615 Fujiwara Dec 2001 A1
20020020890 Willer Feb 2002 A1
20020048200 Kuwazawa Apr 2002 A1
20020048893 Kizilyalli 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
20030222293 Noro Dec 2003 A1
20030227049 Sakakibara Dec 2003 A1
20030227056 Wang 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
20050088889 Lee 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 et al. Jan 2006 A1
20060017092 Dong et al. Jan 2006 A1
20060022252 Doh et al. Feb 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
20060180851 Lee et al. Aug 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
20070022359 Katoh et al. Jan 2007 A1
20070029625 Lue et al. 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
20070158736 Arai et al. Jul 2007 A1
20070200168 Ozawa et al. Aug 2007 A1
20070202708 Luo 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
20080020853 Ingebrigtson 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
20080087946 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
20080173928 Arai et al. Jul 2008 A1
20080175053 Lue et al. Jul 2008 A1
20080230853 Jang et al. Sep 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 et al. 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, Jr. 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
20090039416 Lai 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
20090294828 Ozawa et al. Dec 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
20110233512 Yang et al. Sep 2011 A1
20110237060 Lee et al. Sep 2011 A1
20110248332 Levy et al. Oct 2011 A1
20120007167 Hung et al. Jan 2012 A1
20120061744 Hwang et al. Mar 2012 A1
20120068159 Fujiki et al. Mar 2012 A1
20120068250 Ino et al. Mar 2012 A1
20120068255 Lee et al. Mar 2012 A1
20130048876 Crawford Feb 2013 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
20180366563 Levy et al. Dec 2018 A1
Foreign Referenced Citations (31)
Number Date Country
1107254 Aug 1995 CN
1801478 Jul 2006 CN
1832201 Sep 2006 CN
101517714 Aug 2009 CN
101558481 Oct 2009 CN
101859702 Oct 2010 CN
102142454 Aug 2011 CN
104254921 Dec 2014 CN
2004172616 Jun 2004 JP
2005183940 Jul 2005 JP
2005347679 Dec 2005 JP
2007515060 Jun 2007 JP
2007318112 Dec 2007 JP
2009027134 Feb 2009 JP
2009535800 Oct 2009 JP
2009260070 Nov 2009 JP
2009272348 Nov 2009 JP
2010182939 Aug 2010 JP
2011507231 Mar 2011 JP
2011527824 Nov 2011 JP
2012019211 Jan 2012 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
2007022359 May 2009 WO
2011162725 Dec 2011 WO
2013148112 Oct 2013 WO
2013148343 Oct 2013 WO
Non-Patent Literature Citations (41)
Entry
Lue, Hang-Ting et al., “Reliability Model of Bandgap Engineered SONOS (be-SONOS)”, IEEE, 2006, 4 pgs.
Ohring, Milton, “The Materials Science of Thin Films: Deposition and Structure,” 2nd Edition, Academic Press, 2002, pp. 336-337; 4 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 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.
Altera, “MAX 9000 Programmable Logic Device Family,” Altera, Jul. 1999, Version 6.01, pp. 1-40; 41 pages.
Carley, L. Richard, “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.
Cypress, “1.8V, 500-MHz, 10-Output JEDEC-Compliant Zero Delay Buffer,” Cypress Advance Information, Feb. 12, 2004; 9 pages.
10GEA, “10 Gigabit Ethernet Technology Overview White Paper”, Revision 1.0, Retrieved from Internet: URL: http://www.10gea.org, May 2001.
Cypress, “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.
Cypress, “1K x 8 Dual-Port Static RAM,” Cypress Semiconductor Data Book, May 1995, CY7C130/CY7C131 and CY7C140/C7C141, pp. 6:37-49; 8 pages.
Linear, “1 kHz to 30MHz Resistor Set SOT-23 Oscillator”, Initial Release Final Electrical Specifications LTC1799, Linear Technology Corporation, Jan. 2001, pp. 1-4.
Cypress, “200-MBaud HOTLink Transceiver,” Cypress Semiconductor Corporation, Revised Feb. 13, 2004, CY7C924ADX, Document #38-02008 Rev. *D; 56 pages.
Cypress, “2K x 16 Dual-Port Static RAM,” Cypress Semiconductor Data Book, May 1995, CY7C133 and CY7C143, pp. 6:63-73; 7 pages.
Cypress, “2K x 8 Dual-Port Static RAM,” Cypress Semiconductor Data Book, May 1995, CY7C132/CY7C136 and CY7C142/CY7C146, pp. 6:50-62; 8 pages.
Cypress, “3.3V 64K x 18 Synchronous QuadPort Static RAM,” Cypress Preliminary CY7C0430BV, Cypress Semiconductor Corporation, Mar. 27, 2001; 36 pages.
Takebuchi, Masataka et al. “A Novel Integration Technology of EEPROM Embedded CMOS Logic VLSI Suitable for ASIC Applications”, IEEE 1992 Custom Integrated Circuits Conference, pp. 9.6.1-9.6.4.
Cho, Soon-Jin et al., “A Novel Robust and Low Cost Stack Chips Package and Its Thermal Performance”, IEEE Transaction on Advanced Packaging, vol. 23, No. 2, May 2000, pp. 257-265.
Ohsaki, Katsuhiko et al., “A Planar Type EEPROM Cell Structure by Standard CMOS Process for Integration with Gate Array, Standard Cell, Microprocessor and for Neural Chips”, bIEEE 1993 Custom Integrated Circuits Conference, pp. 23.6.1-23.6A.
Anderson, S. et al., “A Single Chip Sensor & Image Processor for Fingerprint Verification”, IEEE Custom Integrated Circuits Conference, May 12-15, 1991.
Kazerounian, Reza et al., “A Single Poly EPROM for Custom CMOS Logic Applications”, IEEE 1986 Custom Integrated Circuits Conference, pp. 59-62.
Alvarez, Jose et al., “A Wide-Bandwidth Low-Voltage PLL for PowerPC.TM. Microprocessors”, IEEE Journal of Solid-State Circuits, vol. 30, No. 4, Apr. 1995, pp. 383-391.
“About SMaL Camera Technologies, Inc.”, SMaL Camera Technologies, 2001, pp. 1-3.
Duvvury, Charvaka, et al., “Achieving Uniform nMOS Device Power Distribution for Sub-micron ESD Reliability;” Charvaka Duvvuy, Carlos Diaz, and Tim Haddock; 1992; 92-131 through 92-134, no month.
Agilent, “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.h- tml; 2 pages.
Agilent, “ADNS-2051 High-Performance Optical Mouse Sensor,” Agilent Technologies, downloaded Oct. 10, 2005, <http://www.home.agilent.com/USeng/nav/-536893734,536883737/pd.html>.
Agilent, “Agilent ADNK-2030 Solid-State Optical Mouse Sensor,” Agilent Technologies Inc., Sample Kit, 2003; 1 page.
Agilent, “Agilent ADNS-2030 Low Power Optical Mouse Sensor,” Agilent Technologies Inc., Data Sheet, 2005; 34 pages.
Agilent, “Agilent ADNS-2051 Optical Mouse Sensor,” Agilent Technologies Inc., Product Overview, 2003; 2 pages.
Agilent, “Agilent Optical Mouse Sensors,” Agilent Technologies Inc., Selection Guide, 2004; 3 pages.
IBM, “Algorithm for Managing Multiple First-In, First-Out Queues from a Single Shared Random-Access Memory,” IBM Technical Disclosure Bulletin, Aug. 1989; 5 pages.
AMD, “Am99C10A 256.times.48 Content Addressable Memory”, Advanced Micro Devices, Dec. 1992.
Sun, “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.
Cuppens, Roger et al., “An EEPROM for Microprocessors and Custom Logic”, IEEE Journal of Solid-State Circuits, vol. SC-20, No. 2, Apr. 1985, pp. 603-608.
Yoshikawa, Kuniyushi et al.,—“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.
Miyamoto, Jun-Ichi et al., “An Experimental 5-V-Only 256-kbit CMOS EEPROM with a High-Performance Single-Polysilicon Cell”, IEEE Journal of Solid State Circuits, vol. SC-21, No. 5, Oct. 1986, pp. 852-860.
Chien 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.
Chen et al., “Two-bit SONOS type Flash using a band engineering in the nitride layer” Hua-Ching Chien, Chin-Hsing Kao, Jui-Wen Chang and Tzung-Kuen Tsai, Microelectronic Engineering, vol. 80, Jun. 17, 2005_2 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.
Ramkumar, Krishnaswamy, “Cypress SONOS Technology”, Cypress Semiconductor White Paper, Jul. 6, 2011, pp. 1-9.
Lue et al., “Be-SONOS: A Bandgap Engineered SONOS with Excellent Performance and Reliability,” IEEE, 2005; 4 pages.
Related Publications (1)
Number Date Country
20220005929 A1 Jan 2022 US
Provisional Applications (1)
Number Date Country
60940160 May 2007 US
Divisions (1)
Number Date Country
Parent 12152518 May 2008 US
Child 13288919 US
Continuations (5)
Number Date Country
Parent 16600768 Oct 2019 US
Child 17366934 US
Parent 15376282 Dec 2016 US
Child 16600768 US
Parent 15335180 Oct 2016 US
Child 15376282 US
Parent 14811346 Jul 2015 US
Child 15335180 US
Parent 14159315 Jan 2014 US
Child 14811346 US
Continuation in Parts (2)
Number Date Country
Parent 13539466 Jul 2012 US
Child 14159315 US
Parent 13288919 Nov 2011 US
Child 13539466 US