Resistance variable device

Abstract
A method of precluding diffusion of a metal into adjacent chalcogenide material upon exposure to a quanta of actinic energy capable of causing diffusion of the metal into the chalcogenide material includes forming an actinic energy blocking material layer over the metal to a thickness of no greater than 500 Angstroms and subsequently exposing the actinic energy blocking material layer to said quanta of actinic energy. In one implementation, an homogenous actinic energy blocking material layer is formed over the metal and subsequently exposed to said quanta of actinic energy. A method of forming a non-volatile resistance variable device includes providing conductive electrode material over chalcogenide material having metal ions diffused therein. An actinic energy blocking material layer is formed on the conductive electrode material, the actinic energy blocking material layer being effective to shield actinic energy from reaching an interface of the conductive electrode material and the actinic energy blocking material to substantially preclude diffusion of the conductive electrode material into the chalcogenide material upon exposure to said actinic energy. A dielectric layer is formed on the actinic energy blocking material layer. The conductive electrode material is formed into a first electrode. A second electrode is provided proximate the chalcogenide material having the metal diffused therein. Non-volatile resistance variable devices manufacture by these and other methods are contemplated.
Description
TECHNICAL FIELD

This invention relates to non-volatile resistance variable devices and methods of forming the same, and to methods of precluding diffusion of a metal into adjacent chalcogenide material.


BACKGROUND OF THE INVENTION

Semiconductor fabrication continues to strive to make individual electronic components smaller and smaller, resulting in ever denser integrated circuitry. One type of integrated circuitry comprises memory circuitry where information is stored in the form of binary data. The circuitry can be fabricated such that the data is volatile or non-volatile. Volatile storing memory devices result in loss of data when power is interrupted. Non-volatile memory circuitry retains the stored data even when power is interrupted.


This invention was principally motivated in making improvements to the design and operation of memory circuitry disclosed in the Kozicki et al. U.S. Pat. Nos. 5,761,115; 5,896,312; 5,914,893; and 6,084,796, which ultimately resulted from U.S. patent application Ser. No. 08/652,706, filed on May 30, 1.996, disclosing what is referred to as a programmable metalization cell. Such a cell includes opposing electrodes having an insulating dielectric material received therebetween. Received within the dielectric material is a fast ion conductor material. The resistance of such material can be changed between highly insulative and highly conductive states. In its normal high resistive state, to perform a write operation, a voltage potential is applied to a certain one of the electrodes, with the other of the electrode being held at zero voltage or ground. The electrode having the voltage applied thereto functions as an anode, while the electrode held at zero or ground functions as a cathode. The nature of the fast ion conductor material is such that it undergoes a chemical and structural change at a certain applied voltage. Specifically, at some suitable threshold voltage, plating of metal from metal ions within the material begins to occur on the cathode and grows or progresses through the fast ion conductor toward the other anode electrode. With such voltage continued to be applied, the process continues until a single conductive dendrite or filament extends between the electrodes, effectively interconnecting the top and bottom electrodes to electrically short them together.


Once this occurs, dendrite growth stops, and is retained when the voltage potentials are removed. Such can effectively result in the resistance of the mass of fast ion conductor material between electrodes dropping by a factor of 1,000. Such material can be returned to its highly resistive state by reversing the voltage potential between the anode and cathode, whereby the filament disappears. Again, the highly resistive state is maintained once the reverse voltage potentials are removed. Accordingly, such a device can, for example, function as a programmable memory cell of memory circuitry.


The preferred resistance variable material received between the electrodes typically and preferably comprises a chalcogenide material having metal ions diffused therein. A specific example is germanium selenide having silver ions diffused therein. The present method of providing the silver ions within the germanium selenide material is to initially chemical vapor deposit the germanium selenide glass without any silver being received therein. A thin layer of silver is thereafter deposited upon the glass, for example by physical vapor deposition or other technique. An exemplary thickness is 200 Angstroms or less. The layer of silver is irradiated, preferably with electromagnetic energy at a wavelength less than 500 nanometers. The thin nature of the deposited silver enables such energy to pass through the silver to the silver/glass interface effective to break a chalcogenide bond of the chalcogenide material, thereby effecting dissolution of silver into the germanium selenide glass. The applied energy and overlying silver result in the silver migrating into the glass layer such that a homogenous distribution of silver throughout the layer is ultimately achieved.


Saturation of silver in germanium selenide is apparently at about 35 atomic percent. Yet, preferred existing technology for cell fabrication constitutes a concentration which is less than 35%, for example 27%. By controlling the time of irradiation, the quantity of silver provided within the glass can be desirably controlled to some suitable percent below saturation.


However, once the desired irradiation of the silver/glass composite is completed to achieve the desired silver incorporation, the wavelength of radiation required for further dissolution of the silver greatly reduces, even lowering to that of standard room lighting. This is due to the band gap of the underlying material shifting with increasing silver incorporation. Further, and regardless, the substrate is almost invariably next subjected to photolithographic processing resulting in exposure to actinic energy at wavelengths above standard room lighting, which can undesirably cause more silver to be incorporated into the glass than the desired amount.


It would be desirable to develop ways to prevent or at least reduce this additional undesired silver incorporation into the resistance setable material. While the invention was principally motivated in achieving this objective, it is in no way so limited. The artisan will appreciate applicability of the invention in other aspects of processing involving chalcogenide materials, with the invention only being limited by the accompanying claims as literally worded and as appropriately interpreted in accordance with the doctrine of equivalents.


SUMMARY

The invention includes non-volatile resistance variable devices and methods of forming the same, and methods of precluding diffusion of a metal into adjacent chalcogenide material. In one implementation, a method of precluding diffusion of a metal into adjacent chalcogenide material upon exposure to a quanta of actinic energy capable of causing diffusion of the metal into the chalcogenide material includes forming an actinic energy blocking material layer over the metal to a thickness of no greater than 500 Angstroms and subsequently exposing the actinic energy blocking material layer to said quanta of actinic energy. In one implementation, an homogenous actinic energy blocking material layer is formed over the metal and subsequently exposed to said quanta of actinic energy.


In one implementation, a method of forming a non-volatile resistance variable device includes providing conductive electrode material over chalcogenide material having metal ions diffused therein. An actinic energy blocking material layer is formed on the conductive electrode material, the actinic energy blocking material layer being effective to shield actinic energy from reaching an interface of the conductive electrode material and the actinic energy blocking material to substantially preclude diffusion of the conductive electrode material into the chalcogenide material upon exposure to said actinic energy. A dielectric layer is formed on the actinic energy blocking material layer. The conductive electrode material is formed into a first electrode. A second electrode is provided proximate the chalcogenide material having the metal diffused therein.


Other implementations and aspects are contemplated and disclosed.





BRIEF DESCRIPTION OF THE DRAWINGS

Preferred embodiments of the invention are described below with reference to the following accompanying drawings.



FIG. 1 is a diagrammatic sectional view of a semiconductor wafer fragment in process in accordance with an aspect of the invention.



FIG. 2 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 1.



FIG. 3 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 2.



FIG. 4 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 3.



FIG. 5 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 4.



FIG. 6 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 5.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

This disclosure of the invention is submitted in furtherance of the constitutional purposes of the U.S. Patent Laws “to promote the progress of science and useful arts” (Article 1, Section 8).


Referring to FIG. 1, a semiconductor wafer fragment 10 is shown in but one preferred embodiment of a method of forming a non-volatile resistance variable device. By way of example only, example such devices include programmable metalization cells and programmable optical elements of the patents referred to above, further by way of example only, including programmable capacitance elements, programmable resistance elements, programmable antifuses of integrated circuitry and programmable memory cells of memory circuitry. The above patents are herein incorporated by reference. The invention contemplates the fabrication techniques and structure of any existing non-volatile resistance variable device, as well as yet-to-be developed such devices. In the context of this document, the term “semiconductor substrate” or “semiconductive substrate” is defined to mean any construction comprising semiconductive material, including, but not limited to, bulk semiconductive materials such as a semiconductive wafer (either alone or in assemblies comprising other materials thereon), and semiconductive material layers (either alone or in assemblies comprising other materials). The term “substrate” refers to any supporting structure, including, but not limited to, the semiconductive substrates described above. Also in the context of this document, the term “layer” encompasses both the singular and the plural unless otherwise indicated. Further, it will be appreciated by the artisan that “resistance setable semiconductive material” and “resistance variable device” includes materials and devices wherein a property or properties in addition to resistance is/are also varied. For example, and by way of example only, the material's capacitance and/or inductance might also be changed in addition to resistance.


Semiconductor wafer fragment 10 comprises a bulk monocrystalline semiconductive material 12, for example silicon, having an insulative dielectric layer 14, for example silicon dioxide, formed thereover. A conductive electrode material 16 is formed over dielectric layer 14. By way of example only, preferred materials include any of those described in the incorporated Kozicki et al. patents referred to above in conjunction with the preferred type of device being fabricated. A dielectric layer 18 is formed over first electrode 16. Silicon nitride is a preferred example.


An opening 20 is formed through layer 18 to conductive electrode layer 16. Such is filled with a chalcogenide material 22. Example and preferred materials are those disclosed in the Kozicki et al. patents above. Specifically, and by way of example only, preferred chalcogenide materials include GexAy, where “A” is selected from the group consisting of Se, Te and S, and mixtures thereof. An example preferred method of forming material 22 over substrate 10 is by chemical vapor deposition to completely fill opening 20, followed by a planarization technique, for example chemical-mechanical polishing. A metal, shown in the preferred embodiment in the form of a blanket layer 24, is formed over chalcogenide material 22. An example and preferred material for layer 24 is elemental silver. By way of example only, example alternates include gold and copper, although copper is not expected to be usable in the context of the preferred GexAy programmable metalization cell being fabricated. Layer 24 is preferably deposited to a thickness at least one-third that of the thickness of chalcogenide material 22 received within opening 20.


Referring to FIG. 2, metal 24 is irradiated effective to break a chalcogenide bond of the chalcogenide material at an interface of metal 24 and chalcogenide material 22, and diffuse at least some of metal 24 into chalcogenide material 22. Material 22 is designated with numeral 23 and peppered in the drawings to indicate metal ions being received therein. A preferred irradiating includes exposure to actinic radiation having a wavelength below 500 nanometers, with radiation exposure at between 404-408 nanometers being a more specific example. A more specific example is a flood UV exposure tool operating at 4.5 milliwatts/cm2 energy, for 15 minutes, in an oxygen containing ambient at room temperature and pressure.


All of material 24 received directly over chalcogenide material 22 might be diffused to within such material, or some portion thereof might remain as is shown. The thickness of layer 24 is also chosen to be suitably thin to enable the impinging electromagnetic radiation to essentially transparently pass through material 24 to the interface of such material with chalcogenide material 22. An example preferred range for the thickness of layer 24 is from about 140 Angstroms to about 200 Angstroms.


Referring to FIG. 3, after the irradiating, conductive electrode material 26 is formed over chalcogenide material 23 having the metal diffused therein. An example preferred thickness range for electrode material 26 is from 140 Angstroms to 200 Angstroms. Layer 26 and any remnant metal 24 received directly over chalcogenide material 23 will constitute one electrode of the resistance variable device being fabricated, with layer 16 constituting another or second electrode for the device. In accordance with the preferred programmable metalization cell embodiment, at least one of electrode 26/24 and electrode 16 will constitute silver in contact with chalcogenide material 23. Example preferred materials for layer 26 include silver, tungsten and tungsten nitride. Further in the context of this document, any remnant material 24 received over chalcogenide material 23 will form a part of the upper electrode as shown, and accordingly, inherently constitutes conductive electrode material. Accordingly, in the illustrated FIG. 3 embodiment, conductive electrode material 24/26 received over chalcogenide material 23 constitutes two individual layers 24 and 26. In a preferred embodiment, both preferably comprise the same material, specifically silver, and particularly where lower electrode 16 comprises a material other than silver.


Referring to FIG. 4, an actinic energy blocking material layer 28 is formed on conductive electrode material 26/24. In the preferred embodiment, such material layer is effective to shield actinic energy from reaching the interface of materials 26/24 and chalcogenide material 23 to substantially preclude diffusion of metal 24 into chalcogenide material 23 upon exposure to said actinic energy. In one preferred embodiment, layer 28 is insulative. In another preferred embodiment, layer 28 is conductive, thereby forming a part of the illustrated upper electrode. Further in one embodiment, the actinic energy blocking material is actinic energy reflective. In another preferred embodiment, the actinic energy blocking material is actinic energy absorptive and thereby antireflective. By way of example only, example conductive and reflective actinic energy blocking materials include tungsten and tungsten nitride. By way of example only, example actinic energy blocking materials which are both absorptive and insulative include amorphous silicon, silicon oxynitride, silicon-rich silicon nitride, and silicon-rich silicon dioxide.


In the preferred embodiment where a programmable metalization cell is being fabricated which comprises germanium selenide having silver therein, the deposition temperature for providing or otherwise forming layer 28 is preferably at or below 130° C. This is desirable to maintain the preferred embodiment germanium selenide material in a desired operative substantially amorphous state. Actinic energy blocking material 28 is preferably formed to a thickness no greater than 500 Angstroms, and preferably no thinner than 100 Angstroms. Further, actinic energy blocking layer 28 is preferably homogenous in composition, and constitutes a singular layer. Note also that the illustrated layer 26 might be fabricated to constitute an actinic energy blocking material (with or without additional layers) where at least some metal 24 remains over chalcogenide material 23 after the irradiating. In the preferred embodiment, the actinic energy blocking material layer enables the device to be subjected or otherwise exposed to actinic energy which would otherwise be effective to cause more diffusion of metal 24 into chalcogenide material 23, but which is substantially precluded by provision of the actinic energy blocking material.


Referring to FIG. 5, materials 28, 26 and 24 are patterned into an electrode 30. Where layer 28 constitutes conductive material, such forms a part of electrode 30. Where layer 28 comprises an insulative material, such effectively does not constitute a part of the conductive electrode 30, but rather constitutes an insulative material layer received thereover. Patterning to produce electrode 30 is typically and preferably conducted utilizing photolithography whereby actinic energy blocking material layer 28 is inherently exposed to actinic energy, with layer 28 substantially precluding further diffusion of metal layer 24 into chalcogenide material 23.


Referring to FIG. 6, one or more dielectric layers 32 are ultimately formed over actinic energy blocking material layer 28. Of course, intervening conductive and semiconductive layers might also be provided to form other lines and devices outwardly of the depicted device 30.


Independent of the method of fabrication, the invention comprises a non-volatile resistance variable device comprising some substrate having a first electrode formed thereover, for example either electrode 30 or electrode/layer 16. A resistance variable chalcogenide material 23 having metal ions diffused therein is received operatively adjacent the first electrode. A second electrode, for example the other of electrode 30 or electrode/layer 16, is received operatively adjacent the resistance variable chalcogenide material. In one embodiment, an actinic energy blocking material layer is received on the electrode to a thickness of no greater than 500 Angstroms. In one embodiment, a substantially homogenous actinic energy blocking material layer is received on the electrode independent of thickness. Preferably, the actinic energy blocking material layer is both substantially homogenous and of a thickness no greater than 500 Angstroms. In the preferred embodiment, the device is configured as a programmable memory cell, for example the programmable metalization cell as described above.


The invention also constitutes a non-volatile resistance variable device independent of actinic energy blocking effects. In one implementation, such a device comprises a first layer of material which is received on the electrode to a thickness of no greater than 500 Angstroms, with such material being any one or combination of amorphous silicon, silicon oxynitride, silicon-rich silicon nitride, silicon-rich silicon dioxide, tungsten and tungsten nitride. In one embodiment, such a non-volatile resistance variable device comprises a first homogenous layer of material received on the electrode, with such material constituting one or more of amorphous silicon, silicon oxynitride, silicon-rich silicon nitride, silicon-rich silicon dioxide, tungsten and tungsten nitride.


Further, the invention, independent of the device being fabricated, comprises in one embodiment a method of precluding diffusion of a metal into adjacent chalcogenide material upon exposure to a quanta of actinic energy capable of causing diffusion of the metal into the chalcogenide material. In one implementation, such inventive method comprises forming an actinic energy blocking material layer over the metal to a thickness of no greater than 500 Angstroms and subsequently exposing the actinic energy blocking material layer to said quanta of actinic energy. In one implementation, such method includes forming a homogenous actinic energy blocking material layer over the metal and subsequently exposing the actinic energy blocking material layer to said quanta of actinic energy. Most preferably, the actinic energy blocking material layer is both homogenous and provided to a thickness of no greater than 500 Angstroms.


In compliance with the statute, the invention has been described in language more or less specific as to structural and methodical features. It is to be understood, however, that the invention is not limited to the specific features shown and described, since the means herein disclosed comprise preferred forms of putting the invention into effect. The invention is, therefore, claimed in any of its forms or modifications within the proper scope of the appended claims appropriately interpreted in accordance with the doctrine of equivalents.

Claims
  • 1. A resistance variable device comprising: a semiconductor substrate; a first dielectric layer formed over said semiconductor substrate; a first conductive layer formed over said dielectric layer; a second dielectric layer formed over said first conductive layer, said second dielectric layer having an opening exposing said first conductive layer, wherein said opening is filled with a chalcogenide material having metal ions diffused therein; a second conductive layer formed over said first dielectric layer and said chalcogenide material; and an actinic energy blocking material layer formed over said second conductive layer.
  • 2. The device of claim 1, wherein said device is configured to be a programmable memory cell.
  • 3. The device of claim 1, wherein said second conductive layer is about 140 to about 200 Angstroms thick.
  • 4. The device of claim 1, wherein said actinic energy blocking material layer is about 100 to about 500 Angstroms thick.
  • 5. The device of claim 4, wherein said actinic energy blocking material layer is actinic energy reflective.
  • 6. The device of claim 4, wherein said actinic energy blocking material layer is actinic energy absorptive.
  • 7. The device of claim 1, wherein said actinic energy blocking material layer is insulative.
  • 8. The device of claim 1, wherein said actinic energy blocking material layer is conductive.
  • 9. A resistance variable device comprising: a semiconductor substrate; a first conductive layer formed over said semiconductor substrate; a chalcogenide layer formed over said first conductive layer; a second conductive layer formed over said chalcogenide layer, wherein at least a portion of said second conductive layer is diffused into portions of said chalcogenide layer; a third conductive layer formed over said second conductive layer; and an actinic energy blocking material layer formed over said third conductive layer.
  • 10. The device of claim 9, further comprising a first dielectric layer formed between said first conductive layer and said semiconductor substrate.
  • 11. The device of claim 10, further comprising a second dielectric layer formed between said first conductive layer and said chalcogenide layer, wherein at least a portion of said chalcogenide layer remains in contact with said first conductive layer.
  • 12. The device of claim 9, wherein said second conductive layer comprises silver.
  • 13. The device of claim 12, wherein said second conductive layer is formed to be about one-third as thick as said chalcogenide layer.
  • 14. The device of claim 12, wherein said second conductive layer is formed to about 140 to about 200 Angstroms thick.
  • 15. The device of claim 9, wherein said third conductive layer is formed to about 140 to about 200 Angstroms thick.
  • 16. The device of claim 9, wherein said first conductive layer is a bottom electrode.
  • 17. The device of claim 16, wherein said second and third conductive layers are patterned to be a top electrode.
  • 18. The device of claim 16, wherein said second and third conductive layers and said actinic energy blocking material layer are patterned to be a top electrode.
  • 19. The device of claim 18, wherein said actinic energy blocking material layer is conductive.
  • 20. The device of claim 19, wherein said actinic energy blocking material layer comprises tungsten.
  • 21. The device of claim 19, wherein said actinic energy blocking material layer comprises tungsten nitride.
  • 22. The device of claim 9, wherein said actinic energy blocking material layer is about 100 to about 500 Angstroms thick.
  • 23. The device of claim 9, wherein said actinic energy blocking material layer is insulative.
  • 24. A resistance variable device comprising: a semiconductor substrate; a first conductive layer formed over said semiconductor substrate; a chalcogenide layer formed over said first conductive layer with metal ions diffused therein; a second conductive layer formed over said chalcogenide layer; and an actinic energy blocking material layer formed over said second conductive layer, wherein said actinic energy blocking material layer is homogenous in composition.
  • 25. The device of claim 24, further comprising a first dielectric layer formed between said first conductive layer and said semiconductor substrate.
  • 26. The device of claim 25, further comprising a second dielectric layer formed between said first conductive layer and said chalcogenide layer, wherein at least a portion of said chalcogenide layer remains in contact with said first conductive layer.
  • 27. The device of claim 24, wherein said second conductive layer is part of a top electrode.
  • 28. The device of claim 24, wherein said first conductive layer is part of a bottom electrode.
  • 29. The device of claim 24, wherein said second conductive layer is formed to about 140 to about 200 Angstroms thick.
  • 30. The device of claim 24, wherein said actinic energy blocking material layer is about 100 to about 500 Angstroms thick.
  • 31. The device of claim 30, wherein said actinic energy blocking material layer is conductive.
  • 32. The device of claim 30, wherein said actinic energy blocking material layer is insulative.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.: 10/660,602, filed on Sep. 12, 2003 U.S. Pat. No. 6,833,559, which in turn is a divisional of U.S. patent application Ser. No.: 09/779,983, filed on Feb. 8, 2001, now U.S. Pat. No.: 6,638,820. Both applications are incorporated herein by reference.

US Referenced Citations (173)
Number Name Date Kind
3271591 Ovshinsky Sep 1966 A
3622319 Sharp Nov 1971 A
3656029 Ahn et al. Apr 1972 A
3743847 Boland Jul 1973 A
3961314 Klose et al. Jun 1976 A
3966317 Wacks et al. Jun 1976 A
3983542 Ovshinsky Sep 1976 A
3988720 Ovshinsky Oct 1976 A
4177474 Ovshinsky Dec 1979 A
4267261 Hallman et al. May 1981 A
4269935 Masters et al. May 1981 A
4312938 Drexler et al. Jan 1982 A
4316946 Masters et al. Feb 1982 A
4320191 Yoshikawa et al. Mar 1982 A
4405710 Balasubramanyam et al. Sep 1983 A
4419421 Wichelhaus et al. Dec 1983 A
4499557 Holmberg et al. Feb 1985 A
4597162 Johnson et al. Jul 1986 A
4608296 Keem et al. Aug 1986 A
4637895 Ovshinsky et al. Jan 1987 A
4646266 Ovshinsky et al. Feb 1987 A
4664939 Ovshinsky May 1987 A
4668968 Ovshinsky et al. May 1987 A
4670763 Ovshinsky et al. Jun 1987 A
4673957 Ovshinsky et al. Jun 1987 A
4678679 Ovshinsky Jul 1987 A
4696758 Ovshinsky et al. Sep 1987 A
4698234 Ovshinsky et al. Oct 1987 A
4710899 Young et al. Dec 1987 A
4728406 Banerjee et al. Mar 1988 A
4737379 Hudgens et al. Apr 1988 A
4766471 Ovshinsky et al. Aug 1988 A
4769338 Ovshinsky et al. Sep 1988 A
4775425 Guha et al. Oct 1988 A
4788594 Ovshinsky et al. Nov 1988 A
4795657 Formigoni et al. Jan 1989 A
4809044 Pryor et al. Feb 1989 A
4818717 Johnson et al. Apr 1989 A
4843443 Ovshinsky et al. Jun 1989 A
4845533 Pryor et al. Jul 1989 A
4847674 Sliwa et al. Jul 1989 A
4853785 Ovshinsky et al. Aug 1989 A
4891330 Guha et al. Jan 1990 A
5128099 Strand et al. Jul 1992 A
5159661 Ovshinsky et al. Oct 1992 A
5166758 Ovshinsky et al. Nov 1992 A
5177567 Klersy et al. Jan 1993 A
5219788 Abernathey et al. Jun 1993 A
5238862 Blalock et al. Aug 1993 A
5296716 Ovshinsky et al. Mar 1994 A
5315131 Kishimoto et al. May 1994 A
5335219 Ovshinsky et al. Aug 1994 A
5341328 Ovshinsky et al. Aug 1994 A
5350484 Gardner et al. Sep 1994 A
5359205 Ovshinsky Oct 1994 A
5360981 Owen et al. Nov 1994 A
5406509 Ovshinsky et al. Apr 1995 A
5414271 Ovshinsky et al. May 1995 A
5500532 Kozicki et al. Mar 1996 A
5512328 Yoshimura et al. Apr 1996 A
5512773 Wolf et al. Apr 1996 A
5534711 Ovshinsky et al. Jul 1996 A
5534712 Ovshinsky et al. Jul 1996 A
5536947 Klersy et al. Jul 1996 A
5543737 Ovshinsky Aug 1996 A
5591501 Ovshinsky et al. Jan 1997 A
5596522 Ovshinsky et al. Jan 1997 A
5687112 Ovshinsky Nov 1997 A
5694054 Ovshinsky et al. Dec 1997 A
5714768 Ovshinsky et al. Feb 1998 A
5726083 Takaishi Mar 1998 A
5751012 Wolstenholme et al. May 1998 A
5761115 Kozicki et al. Jun 1998 A
5789277 Zahorik et al. Aug 1998 A
5825046 Czubatyj et al. Oct 1998 A
5841150 Gonzalez et al. Nov 1998 A
5846889 Harbison et al. Dec 1998 A
5896312 Kozicki et al. Apr 1999 A
5912839 Ovshinsky et al. Jun 1999 A
5914893 Kozicki et al. Jun 1999 A
5920788 Reinberg Jul 1999 A
5933365 Klersy et al. Aug 1999 A
5998066 Block et al. Dec 1999 A
6011757 Ovshinsky Jan 2000 A
6077729 Harshfield Jun 2000 A
6084796 Kozicki et al. Jul 2000 A
6087674 Ovshinsky et al. Jul 2000 A
6117720 Harshfield Sep 2000 A
6141241 Ovshinsky et al. Oct 2000 A
6143604 Chiang et al. Nov 2000 A
6177338 Liaw et al. Jan 2001 B1
6236059 Wolsteinholme et al. May 2001 B1
RE37259 Ovshinsky Jul 2001 E
6297170 Gabriel et al. Oct 2001 B1
6300684 Gonzalez et al. Oct 2001 B1
6316784 Zahorik et al. Nov 2001 B1
6329606 Freyman et al. Dec 2001 B1
6339544 Chiang et al. Jan 2002 B1
6348365 Moore et al. Feb 2002 B1
6350679 McDaniel et al. Feb 2002 B1
6376284 Gonzalez et al. Apr 2002 B1
6388324 Kozicki et al. May 2002 B1
6391688 Gonzalez et al. May 2002 B1
6404665 Lowery et al. Jun 2002 B1
6414376 Thakur et al. Jul 2002 B1
6418049 Kozicki et al. Jul 2002 B1
6423628 Li et al. Jul 2002 B1
6429064 Wicker Aug 2002 B1
6437383 Xu Aug 2002 B1
6462984 Xu et al. Oct 2002 B1
6469364 Kozicki Oct 2002 B1
6480438 Park Nov 2002 B1
6487106 Kozicki Nov 2002 B1
6487113 Park et al. Nov 2002 B1
6501111 Lowery Dec 2002 B1
6507061 Hudgens et al. Jan 2003 B1
6511862 Hudgens et al. Jan 2003 B1
6511867 Lowery et al. Jan 2003 B1
6512241 Lai Jan 2003 B1
6514805 Xu et al. Feb 2003 B1
6531373 Gill et al. Mar 2003 B1
6534781 Dennison Mar 2003 B1
6545287 Chiang Apr 2003 B1
6545907 Lowery et al. Apr 2003 B1
6555860 Lowery et al. Apr 2003 B1
6563164 Lowery et al. May 2003 B1
6566700 Xu May 2003 B1
6567293 Lowery et al. May 2003 B1
6569705 Chiang et al. May 2003 B1
6570784 Lowery May 2003 B1
6576921 Lowery Jun 2003 B1
6586761 Lowery Jul 2003 B1
6589714 Maimon et al. Jul 2003 B1
6590807 Lowery Jul 2003 B1
6593176 Dennison Jul 2003 B1
6597009 Wicker Jul 2003 B1
6605527 Dennison et al. Aug 2003 B1
6613604 Maimon et al. Sep 2003 B1
6621095 Chiang et al. Sep 2003 B1
6625054 Lowery et al. Sep 2003 B1
6638820 Moore Oct 2003 B1
6642102 Xu Nov 2003 B1
6646297 Dennison Nov 2003 B1
6649928 Dennison Nov 2003 B1
6667900 Lowrey et al. Dec 2003 B1
6671710 Ovshinsky et al. Dec 2003 B1
6673648 Lowrey Jan 2004 B1
6673700 Dennison et al. Jan 2004 B1
6674115 Hudgens et al. Jan 2004 B1
6687153 Lowery Feb 2004 B1
6687427 Ramalingam et al. Feb 2004 B1
6690026 Peterson Feb 2004 B1
6696355 Dennison Feb 2004 B1
6707712 Lowery Mar 2004 B1
6714954 Ovshinsky et al. Mar 2004 B1
6833559 Moore Dec 2004 B1
20020000666 Kozicki et al. Jan 2002 A1
20020072188 Gilton Jun 2002 A1
20020123169 Moore et al. Sep 2002 A1
20020123248 Moore et al. Sep 2002 A1
20020168820 Kozicki Nov 2002 A1
20030027416 Moore et al. Feb 2003 A1
20030045049 Campbell et al. Mar 2003 A1
20030045054 Campbell et al. Mar 2003 A1
20030048744 Ovshinsky et al. Mar 2003 A1
20030049912 Campbell et al. Mar 2003 A1
20030050124 Kanamaru et al. Mar 2003 A1
20030107105 Kozicki Jun 2003 A1
20030137869 Kozicki Jul 2003 A1
20030143782 Gilton et al. Jul 2003 A1
20030212724 Ovshinsky et al. Nov 2003 A1
20030212725 Ovshinsky et al. Nov 2003 A1
20040035401 Ramachandran et al. Feb 2004 A1
Foreign Referenced Citations (5)
Number Date Country
56126916 Oct 1981 JP
WO 9748032 Dec 1997 WO
WO 9928914 Jun 1999 WO
WO 0048196 Aug 2000 WO
WO 0221542 Mar 2002 WO
Related Publications (1)
Number Date Country
20050019699 A1 Jan 2005 US
Divisions (1)
Number Date Country
Parent 09779983 Feb 2001 US
Child 10660602 US
Continuations (1)
Number Date Country
Parent 10660602 Sep 2003 US
Child 10920333 US