Method for forming self-aligned thermal isolation cell for a variable resistance memory array

Information

  • Patent Grant
  • 7923285
  • Patent Number
    7,923,285
  • Date Filed
    Friday, January 9, 2009
    15 years ago
  • Date Issued
    Tuesday, April 12, 2011
    13 years ago
Abstract
A non-volatile memory with a self-aligned RRAM element includes a lower electrode element, generally planar in form, having an inner contact surface; an upper electrode element, spaced from the lower electrode element; a containment structure extends between the upper electrode element and the lower electrode element, with a sidewall spacer element having a generally funnel-shaped central cavity with a central aperture; and a spandrel element positioned between the sidewall spacer element and the lower electrode. A RRAM element extends between the lower electrode element and the upper electrode, occupying at least a portion of the sidewall spacer element central cavity and projecting from the sidewall spacer terminal edge toward and making contact with the lower electrode. In this manner, the spandrel element inner surface is spaced from the RRAM element to define a thermal isolation cell adjacent the RRAM element.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates to non-volatile memory structures, and more specifically to memory devices employing Resistance Random Access Memory (RRAM) memory elements.


2. Description of Related Art


RRAM based memory materials are widely used in read-write optical disks and non-volatile memory arrays. These materials have at least two solid phases, including for example a generally amorphous solid phase and a generally crystalline solid phase. Laser pulses are used in read-write optical disks to switch between phases and to read the optical properties of the material after the RRAM.


RRAM based memory materials, such as chalcogenide based materials and similar materials, also can be caused to change phase by application of electrical current at levels suitable for implementation in integrated circuits. The generally amorphous state is characterized by higher resistivity than the generally crystalline state, which can be readily sensed to indicate data. These properties have generated interest in using programmable resistive material to form nonvolatile memory circuits, which can be read and written with random access.


The change from the amorphous to the crystalline state is generally a lower current operation. The change from crystalline to amorphous, referred to as reset herein, is generally a higher current operation, which includes a short high current density pulse to melt or breakdown the crystalline structure, after which the RRAM material cools quickly, quenching the RRAM process, allowing at least a portion of the RRAM structure to stabilize in the amorphous state. It is desirable to minimize the magnitude of the reset current used to cause transition of RRAM material from crystalline state to amorphous state. The magnitude of the reset current needed for reset can be reduced by reducing the size of the RRAM material element in the cell and of the contact area between electrodes and the RRAM material, so that higher current densities are achieved with small absolute current values through the RRAM material element.


One direction of development has been toward forming small pores in an integrated circuit structure, and using small quantities of programmable resistive material to fill the small pores. Patents illustrating development toward small pores include: Ovshinsky, “Multibit Single Cell Memory Element Having Tapered Contact,” U.S. Pat. No. 5,687,112, issued Nov. 11, 1997; Zahorik et al., “Method of Making Chalogenide [sic] Memory Device,” U.S. Pat. No. 5,789,277, issued Aug. 4, 1998; Doan et al., “Controllable Ovonic Phase-Change Semiconductor Memory Device and Methods of Fabricating the Same,” U.S. Pat. No. 6,150,253, issued Nov. 21, 2000.


Problems have arisen in manufacturing such devices with very small dimensions, and with variations in process that meets tight specifications needed for large-scale memory devices. It is desirable therefore to provide a memory cell structure having small dimensions and low reset currents, and a method for manufacturing such structure that meets tight process variation specifications needed for large-scale memory devices. It is further desirable to provide a manufacturing process and a structure, which are compatible with manufacturing of peripheral circuits on the same integrated circuit.


SUMMARY OF THE INVENTION

A non-volatile memory device with a self-aligned RRAM element. The memory device includes a lower electrode element, generally planar in form, having an inner contact surface. At the top of the device is an upper electrode element, spaced from the lower electrode element. A containment structure extends between the upper electrode element and the lower electrode element, and this element includes a sidewall spacer element having an inner surface defining a generally funnel-shaped central cavity, terminating at a terminal edge to define a central aperture; and a spandrel element positioned between the sidewall spacer element and the lower electrode, having an inner surface defining a thermal isolation cell, the spandrel inner walls being spaced radially outward from the sidewall spacer terminal edge, such that the sidewall spacer terminal edge projects radially inward from the spandrel element inner surface. A RRAM element extends between the lower electrode element and the upper electrode, occupying at least a portion of the sidewall spacer element central cavity and projecting from the sidewall spacer terminal edge toward and making contact with the lower electrode. In this manner, the spandrel element inner surface is spaced from the RRAM element to define a thermal isolation cell adjacent the RRAM element.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 illustrates an embodiment of a variable resistance memory element as claimed herein.



FIG. 1
a depicts the sidewall portion of the embodiment of FIG. 1.



FIGS. 2
a-2h illustrate an embodiment of a process for fabricating the embodiment of FIG. 1.





DETAILED DESCRIPTION

The following detailed description is made with reference to the figures. Preferred embodiments are described to illustrate the present invention, not to limit its scope, which is defined by the claims. Those of ordinary skill in the art will recognize a variety of equivalent variations on the description that follows.


A memory element 10 is illustrated in FIG. 1. The element is fabricated on a substrate, or inter-layer dielectric layer, 12. The following discussion sets out the structure of this element, with the fabrication process following shortly thereafter. This layer preferably consists of silicon oxide or a well-known alternative thereto, such as a polyimide, silicon nitride or other dielectric fill material. In embodiments, the dielectric layer comprises a relatively good insulator for heat as well as for electricity, providing thermal and electrical isolation. An electrical contact, or plug, 14, preferably formed from a refractory metal such as tungsten, is formed in the oxide layer. Other refractory metals include Ti, Mo, Al, Ta, Cu, Pt, Ir, La, Ni, and Ru. The plug element makes electrical contact with an isolation or switching device, such as a transistor, located below the dielectric layer 12, as is known in the art. Other circuit components preferably located below the illustrated RRAM element include the common source lines and word lines, both of which are well-known in the memory art.


It should be noted that, for purposes of reference only, the direction from the bottom toward the top of the drawings herein is designated “vertical”, and the side-to-side direction is “lateral” or “horizontal.” Thus, “width” denotes a dimension parallel to the horizontal direction in the drawings, and “height” or “thickness” denotes a dimension parallel to the vertical. Such designations have no effect on the actual physical orientation of a device, either during fabrication or during use.


An lower electrode element 16 is formed atop the plug element 14. The lower electrode is preferably generally tabular in form and can be slightly wider than the plug element. It is formed from a metal such as copper, but other types of metallization, including aluminum, titanium nitride, and tungsten based materials can be utilized as well. Also, non-metal conductive material such as doped polysilicon can be used. The electrode material in the illustrated embodiment is preferably TiN or TaN. Alternatively, the lower electrodes may be TiAlN or TaAlN, or may comprise, for further examples, one or more elements selected from the group consisting of Ti, W, Mo, Al, Ta, Cu, Pt, Ir, La, Ni, and Ru and alloys thereof.


A spandrel element 18 is formed on the lower electrode element. As will be understood better in considering the spandrel element in the context of the embodiment as a whole, the material of which this element is composed will depend on choices made for adjacent layers. In general it can be said that that the overall criteria for this element are that it first function effectively as a spandrel in the environment of a memory device, and second that it offer the possibility of a highly selective etching process, as described below. Thus, the material to be employed here depends upon the materials chosen for the lower electrode element 16, discussed above, and the sidewall spacer element 21, discussed above. If, for example, the lower electrode element is composed of TiN, as is preferable, then suitable materials for the spandrel element could be W or Al or SiN, all of which offer the possibility of a high differential etch rate, as discussed below.


Sidewall spacer element 21 lies above and in contact with the spandrel element. This element is relatively thick compared with the lower electrode and spandrel, but it is coextensive with those elements in width. FIG. 1a is a detailed view of the sidewall spacer element, allowing its structure to be viewed more clearly. As can be seen there, the sidewall spacer element has a central cavity 32, generally funnel-shaped in form, with inner sides 38 of the sidewall spacer having a convex profile. The inner sides intersect with the bottom of the sidewall spacer to form terminal edges 34, which in turn define a central aperture 36. The sidewall spacer element is formed from a dielectric fill material.


As shown in FIG. 1, a portion of the sidewall spacer central cavity is filled with a RRAM element 22. This element fills the lower portion of the central cavity and extends downward to make contact with the lower electrode element.


The phase-change element 22 is formed from a material that can assume at least two stable resistance levels, referred to as resistance random access memory (RRAM) material. Several materials have proved useful in fabricating RRAM, as described below.


An important class of RRAM material is the chalcogenide group. Chalcogens include any of the four elements oxygen (O), sulfur (S), selenium (Se), and tellurium (Te), forming part of group VI of the periodic table. Chalcogenides comprise compounds of a chalcogen with a more electropositive element or radical. Chalcogenide alloys comprise combinations of chalcogenides with other materials such as transition metals. A chalcogenide alloy usually contains one or more elements from column six of the periodic table of elements, such as germanium (Ge) and tin (Sn). Often, chalcogenide alloys include combinations including one or more of antimony (Sb), gallium (Ga), indium (In), and silver (Ag). Because chalcogenides achieve their dual-memory capabilities by forming two solid phases, each of which exhibits a characteristic resistance, these materials are referred to as “RRAM” materials or alloys.


Many RRAM based memory materials have been described in technical literature, including alloys of: Ga/Sb, In/Sb, In/Se, Sb/Te, Ge/Te, Ge/Sb/Te, In/Sb/Te, Ga/Se/Te, Sn/Sb/Te, In/Sb/Ge, Ag/In/Sb/Te, Ge/Sn/Sb/Te, Ge/Sb/Se/Te and Te/Ge/Sb/S. In the family of Ge/Sb/Te alloys, a wide range of alloy compositions may be workable. The compositions can be characterized as TeaGebSb100−(a+b). One researcher has described the most useful alloys as having an average concentration of Te in the deposited materials well below 70%, typically below about 60% and ranged in general from as low as about 23% up to about 58% Te and most preferably about 48% to 58% Te. Concentrations of Ge were above about 5% and ranged from a low of about 8% to about 30% average in the material, remaining generally below 50%. Most preferably, concentrations of Ge ranged from about 8% to about 40%. The remainder of the principal constituent elements in this composition was Sb. These percentages are atomic percentages that total 100% of the atoms of the constituent elements. (Ovshinsky '112 patent, cols 10-11.) Particular alloys evaluated by another researcher include Ge2Sb2Te5, GeSb2Te4 and GeSb4Te7. (Noboru Yamada, “Potential of Ge-Sb-Te Phase-Change Optical Disks for High-Data-Rate Recording”, SPIE v.3109, pp. 28-37 (1997).) More generally, a transition metal such as chromium (Cr), iron (Fe), nickel (Ni), niobium (Nb), palladium (Pd), platinum (Pt) and mixtures or alloys thereof may be combined with Ge/Sb/Te to form a RRAM alloy that has programmable resistive properties. Specific examples of memory materials that may be useful are given in Ovshinsky '112 at columns 11-13, which examples are hereby incorporated by reference.


RRAM alloys are capable of being switched between a first structural state in which the material is in a generally amorphous solid phase, and a second structural state in which the material is in a generally crystalline solid phase in its local order in the active channel region of the cell. These alloys are at least bistable. The term amorphous is used to refer to a relatively less ordered structure, more disordered than a single crystal, which has the detectable characteristics such as higher electrical resistivity than the crystalline phase. The term crystalline is used to refer to a relatively more ordered structure, more ordered than in an amorphous structure, which has detectable characteristics such as lower electrical resistivity than the amorphous phase. Typically, RRAM materials may be electrically switched between different detectable states of local order across the spectrum between completely amorphous and completely crystalline states. Other material characteristics affected by the change between amorphous and crystalline phases include atomic order, free electron density and activation energy. The material may be switched either into different solid phases or into mixtures of two or more solid phases, providing a gray scale between completely amorphous and completely crystalline states. The electrical properties in the material may vary accordingly.


RRAM alloys can be changed from one phase state to another by application of electrical pulses. It has been observed that a shorter, higher amplitude pulse tends to change the RRAM material to a generally amorphous state. A longer, lower amplitude pulse tends to change the RRAM material to a generally crystalline state. The energy in a shorter, higher amplitude pulse is high enough to allow for bonds of the crystalline structure to be broken and short enough to prevent the atoms from realigning into a crystalline state. Appropriate profiles for pulses can be determined, without undue experimentation, specifically adapted to a particular RRAM alloy. In following sections of the disclosure, the RRAM material is referred to as GST, and it will be understood that other types of RRAM materials can be used. A material useful for implementation of a PCRAM described herein is Ge2Sb2Te5.


Other programmable resistive memory materials may be used in other embodiments of the invention. One such material is a colossal magnetoresistance (CMR) material, which dramatically change resistance levels in the presence of a magnetic field. Such materials are generally manganese-based perovskite oxides, and the resistance changes encountered are generally in the range of orders of magnitude. A preferred formulation for RRAM applications is PrxCayMnO3, where x:y=0.5:0.5, or other compositions in which x:0˜1; y:0˜1. Other CMR materials including an Mn oxide can also be employed.


Another RRAM material is a 2-element compound, such as NixOy; TixOy; AlxOy; WxOy; ZnxOy; ZrxOy; CuxOy, where x:y=0.5:0.5. Alternatively, another compound in this group could be employed, in which x:0˜1; y:0˜1. Also, polymers employing dopants such as Cu, C60, Ag can be employed, including 7,7,8,8-tetracyanoquinodimethane (TCNQ), methanofullerene 6,6-phenyl C61-butyric acid methyl ester (PCBM), TCNQ-PCBM, Cu-TCNQ, Ag-TCNQ, C60-TCNQ, TCNQ doped with other metal, or any other polymer material that has bistable or multi-stable resistance state controlled by an electrical pulse.


Here the relationship between the sidewall spacer element, the RRAM element, the spandrel element and the lower electrode element should be noted. The spandrel element lies between the lower electrode and sidewall spacer elements, but the inner edges 19 of the spandrel element do not extend to make contact with the lower portion of the RRAM element. Rather, the spandrel inner edges are recessed from the sidewall spacer element terminal edges, so that the sidewall spacer, spandrel, lower electrode and RRAM elements enclose a void surrounding the RRAM element, thermal isolation cell 20. The spandrel element is surrounded by an inter-metal dielectric layer 24, which is preferably a dielectric fill material, such as SiO2.


Upper electrode element 26 lies on the sidewall spacer element, and a portion of the upper electrode extends into the central cavity to make electrical contact with RRAM element 22. This element is preferably formed from TiN or similar material, as discussed above. This electrode provides contact with other circuit elements, and in one embodiment it is in direct electrical contact a bit line (not shown).


Operation of the embodiment of FIG. 1 proceeds as follows. As noted above, the memory element 10 stores a data bit by altering the solid phase of RRAM element 22, causing the electrical resistance of that device to change as well. In its crystalline phase state, the RRAM element has a relatively low electrical resistance, while in the amorphous state its resistance is relatively high. Thus, one state can be chosen to represent a logical one and the other a logical zero, also referred to in the art as “high” and “low” logic levels. Thus, two signals are required to set the device state, a SET signal and one for RESET, chosen to produce the desired RRAM in the element. In one embodiment, the default level for the device is chosen to be the logical zero, or low, which is chosen to correspond to the high resistance (amorphous) state. Thus, the RESET signal is chosen as appropriate to produce the amorphous state. The SET signal, to produce the logic one level, is likewise chosen to produce the crystalline state. One other operation must be provided for, to sense a present level of the device in a READ operation. That signal is chosen below the level that will produce any RRAM.


These signals are generally initiated in control circuitry (not shown) which communicates with the circuitry immediately concerned with the memory element shown. In one embodiment such initiation proceeds by energizing the word line associated with the transistor controlling the element, turning that transistor on so that current flows through the transistor to plug element 14 and then through lower electrode 16, RRAM element 22 and upper electrode 26 and out to the bit line (not shown). That high current density in the most narrow area 28 of RRAM element 22 produces joule heating, which in turn leads to RRAM. The area 28 is by design located in the area of thermal isolation cell 20.


An embodiment of the process for fabricating the memory element of FIG. 1 is shown in FIGS. 2a-2h. Discussions above on the materials employed will not be repeated here.


The process begins with deposition of the substrate, or inter-layer dielectric (ILD) 12, as depicted in FIG. 2a. Next, the plug element 14 is formed through the ILD, preferably by lithographically etching the opening and depositing the electrode material, followed by planarizing the ILD to remove any excess electrode material. Then three layers are deposited in succession—an electrode layer 16, a spandrel layer 18 and a sacrificial layer 23. Deposition of these layers can proceed as known in the art. The sacrificial layer 23 is preferably composed of silicon nitride, primarily for its ability to be preferentially etched in comparison with silicon dioxide. Following deposition, the width of these three layers is trimmed to a desired value, preferably employing conventional lithographic and etching methods.


Next, as seen in FIG. 2c, an inter-metal dielectric layer (IMD) 24 is deposited or grown on the ILD, surrounding the trimmed layers. This layer is composed of suitable dielectric fill material, as discussed above. A planarization process, such as chemical-mechanical polishing (CMP) is employed to reduce the thickness of the newly-formed dielectric layer to a desired thickness, exposing the nitride layer 23. Next, as seen in FIG. 2d, the nitride layer is removed, leaving a void 27 in the upper surface of the IMD.



FIG. 2
e depicts the initial formation of sidewall spacer 21, which is formed by deposition followed by etching, to produce a structure having a profile with convex sides of increasing thickness from top to bottom. Those in the art will understand that a number of known processes exist to accomplish this step, including the technique of sidewall spacer patterning. To accomplish that result, a layer of suitable material, such as an oxide dielectric material, is deposited on the structure shown in FIG. 2d. That material is then anisotropically etched to remove all material down to the level of the IMD 24, leaving a sidewall spacer 21 having sloping walls and a funnel-shaped central cavity 32, as discussed above. The etchant for this process is dependent on the exact materials, but assuming the spandrel 18 is W, then the preferred etchant for the oxide material is CHF3/CHF4 or CH3F/CHF4. either of those choices is highly selective for the oxide over the tungsten material.


In the next step, the thermal isolation cell is formed, as shown in FIG. 2f. Preferably, this etching step is performed via a plasma etch, using a no-bias, isotropic process. Here the preferred etchant is SF6/O2, which will etch the oxide and TiN layers at a significantly slower rate than the W material of the spandrel. Of course, different materials will require a change in the etch material recipe.


The etchant acts selectively on the spandrel, leaving the sidewall spacer and underlying electrode relatively unaffected. The result is that the spandrel element is removed altogether in its central portion, with inner edges 19 substantially recessed from the central opening of the sidewall spacer.


Next, in FIG. 2g, the RRAM element 22 is added, preferably by a deposition process. Here it is preferred to carry out the deposition with a sputtering process, which will produce a more conformal coating. Owing to the inward-sloping shape of the sidewall spacer, and its central opening, deposited GST material accumulates on the upper surface of electrode 16, building upward until it reaches the level of the sidewall spacer central opening, and thereafter the GST material proceeds to fill the sidewall spacer central cavity. It is preferred to continue the GST deposition until the sidewall spacer is filled, which also produces a layer of GST material on the ILD layer. A selective etching step is then undertaken, which removes all GST material on the ILD layer. In one embodiment, the etch is continued until the GST material is recessed into the sidewall spacer central cavity, as shown in FIG. 2g. This measure is preferred in order to ensure good contact between the RRAM element and the succeeding layer, as explained below. After this step, the RRAM element 22 is a flared shape, with its narrow end in contact with electrode 16. As a further consequence of the operations on the sidewall spacer, the RRAM element is self-aligned in the cell, centered on the electrode. Also, it is desirable that the narrowest segment of the RRAM element be just below the terminal edge of the sidewall spacer, and the sidewall spacer geometry can be designed to provide that result, as shown.


The final step is shown in FIG. 2h, in which the upper electrode 26 is deposited. This element, formed of TiN, as discussed above, is deposited, according to methods known in the art, so that material fills the remainder of the sidewall spacer, making contact with the RRAM element, and then forms a layer atop the ILD. The layer is reduced to a desired thickness, preferably using a CMP process, and then lithographically trimmed to a desired width, with the result as shown.


While the present invention is disclosed by reference to the preferred embodiments and examples detailed above, it is to be understood that these examples are intended in an illustrative rather than in a limiting sense. It is contemplated that modifications and combinations will readily occur to those skilled in the art, which modifications and combinations will be within the spirit of the invention and the scope of the following claims.

Claims
  • 1. A method of fabricating a memory device, comprising: providing a bottom electrode;forming a dielectric element over the bottom electrode;forming a via in the dielectric element;forming a spacer element and a memory element in the via; andforming a top electrode over the memory element;wherein there is an opening between the memory element and the spacer element within the via.
  • 2. The method of claim 1, wherein forming the via is by etching the dielectric element.
  • 3. The method of claim 1, wherein forming the spacer dielectric element and the memory element is by a depositing process.
  • 4. A method of fabricating a memory device, comprising: providing a dielectric layer;etching the dielectric layer to form a via;forming a first electrode in the via;depositing a sidewall element in the via;depositing a memory element over the sidewall element; andforming a second electrode over the memory element;wherein the sidewall element is spaced away from the first electrode having inner surface which with a top surface of the bottom electrode defines an opening within the via on the first electrode.
  • 5. A method of fabricating a memory device, comprising the steps of: providing a substrate of insulating material;depositing successively a lower electrode layer, a spandrel layer and a sacrificial layer on the substrate, trimming those layers to form a lower electrode element, a spandrel element and a sacrificial element, and depositing an insulating layer to enclose and surround the same;etching the sacrificial element to form a void over the lower electrode element and spandrel element in the insulating layer surface;forming a sidewall spacer element having a generally funnel-shaped opening in the void, having a terminal edge at the bottom of the opening, thereby exposing the spandrel layer;selectively isotropically etching the spandrel element to extend the opening through the spandrel element to the lower electrode, such that a spandrel element inner surface is defined, recessed from the terminal edge of the sidewall spacer element;depositing a programmable resistive material into the opening, such that a portion of the programmable resistive material is in contact with the sidewall spacer element inner surface and a portion extends from the sidewall spacer element terminal edge to make contact with the lower electrode; andforming an upper electrode in contact with the programmable resistive material;whereby the spandrel element inner surface and the programmable resistive material define a thermal isolation cell.
  • 6. The method of claim 5, wherein the programmable resistive material comprises a combination of Ge, Sb, and Te.
  • 7. The method of claim 5, wherein the programmable resistive material comprises a combination of two or more materials from the group of Ge, Sb, Te, Se, In, Ti, Ga, Bi, Sn, Cu, Pd, Pb, Ag, S, and Au.
  • 8. The method of claim 5, wherein the programmable resistive material exhibits variable resistance, such variability being associated with changes in phase structure.
  • 9. The method of claim 5, wherein the spandrel element is composed of a material exhibiting high preferential etch properties relative to the sidewall spacer and lower electrode elements.
  • 10. The method of claim 5, wherein the spandrel element is composed of tungsten, the sidewall spacer element is composed of a dielectric fill oxide, and the lower electrode is composed of TiN.
  • 11. The method of claim 5, wherein the upper electrode element extends into and partially fills the central cavity, making contact therein with the programmable resistive material.
REFERENCE TO RELATED APPLICATIONS

This application is a divisional of application Ser. No. 11/463,824 filed on 10 Aug. 2006, which application claims the benefit of U.S. Provisional Patent Application No. 60/754,161, entitled “Method for Forming Self-Aligned Thermal Isolation Cell for a Phase Change Memory Array” filed on 27 Dec. 2005.

US Referenced Citations (323)
Number Name Date Kind
3271591 Ovshinsky Sep 1966 A
3530441 Ovshinsky Sep 1970 A
4452592 Tsai Jun 1984 A
4599705 Holmberg et al. Jul 1986 A
4719594 Young et al. Jan 1988 A
4769339 Ishii et al. Sep 1988 A
4876220 Mohsen et al. Oct 1989 A
4959812 Momodomi et al. Sep 1990 A
5106775 Kaga et al. Apr 1992 A
5166096 Cote et al. Nov 1992 A
5166758 Ovshinsky et al. Nov 1992 A
5177567 Klersy et al. Jan 1993 A
5332923 Takeuchi et al. Jul 1994 A
5391901 Tanabe et al. Feb 1995 A
5515488 Hoppe et al. May 1996 A
5534712 Ovshinsky et al. Jul 1996 A
5550396 Tsutsumi et al. Aug 1996 A
5687112 Ovshinsky Nov 1997 A
5688713 Linliu et al. Nov 1997 A
5716883 Tseng et al. Feb 1998 A
5754472 Sim et al. May 1998 A
5789277 Zahorik et al. Aug 1998 A
5789758 Reinberg Aug 1998 A
5807786 Chang et al. Sep 1998 A
5814527 Wolstenholme et al. Sep 1998 A
5831276 Gonzalez et al. Nov 1998 A
5837564 Sandhu et al. Nov 1998 A
5869843 Harshfield Feb 1999 A
5879955 Gonzalez et al. Mar 1999 A
5902704 Schoenborn et al. May 1999 A
5920788 Reinberg Jul 1999 A
5933365 Klersy et al. Aug 1999 A
5952671 Reinberg et al. Sep 1999 A
5958358 Tenne et al. Sep 1999 A
5970336 Wolstenholme et al. Oct 1999 A
5985698 Gonzalez et al. Nov 1999 A
5998244 Wolstenholme et al. Dec 1999 A
6011725 Eitan et al. Jan 2000 A
6025220 Sandhu Feb 2000 A
6031287 Harshfield Feb 2000 A
6034882 Johnson et al. Mar 2000 A
6046951 El Hajji et al. Apr 2000 A
6066870 Siek May 2000 A
6077674 Schleifer et al. Jun 2000 A
6077729 Harshfield Jun 2000 A
6087269 Williams Jul 2000 A
6087674 Ovshinsky et al. Jul 2000 A
6104038 Gonzalez et al. Aug 2000 A
6111264 Wolstenholme et al. Aug 2000 A
6114713 Zahorik Sep 2000 A
6117720 Harshfield Sep 2000 A
6147395 Gilgen Nov 2000 A
6150253 Doan et al. Nov 2000 A
6153890 Wolstenholme et al. Nov 2000 A
6177317 Huang et al. Jan 2001 B1
6185122 Johnson et al. Feb 2001 B1
6189582 Reinberg et al. Feb 2001 B1
6236059 Wolstenholme et al. May 2001 B1
RE37259 Ovshinsky Jul 2001 E
6271090 Huang et al. Aug 2001 B1
6280684 Yamada et al. Aug 2001 B1
6287887 Gilgen Sep 2001 B1
6291137 Lyons et al. Sep 2001 B1
6314014 Lowrey et al. Nov 2001 B1
6316348 Fu et al. Nov 2001 B1
6320786 Chang et al. Nov 2001 B1
6326307 Lindley et al. Dec 2001 B1
6339544 Chiang et al. Jan 2002 B1
6351406 Johnson et al. Feb 2002 B1
6372651 Yang et al. Apr 2002 B1
6380068 Jeng et al. Apr 2002 B2
6420215 Knall et al. Jul 2002 B1
6420216 Clevenger et al. Jul 2002 B1
6420725 Harshfield Jul 2002 B1
6423621 Doan et al. Jul 2002 B2
6429064 Wicker Aug 2002 B1
6440837 Harshfield Aug 2002 B1
6462353 Gilgen Oct 2002 B1
6483736 Johnson et al. Nov 2002 B2
6487114 Jong et al. Nov 2002 B2
6489645 Uchiyama Dec 2002 B1
6501111 Lowrey Dec 2002 B1
6507061 Hudgens et al. Jan 2003 B1
6511867 Lowrey et al. Jan 2003 B2
6512241 Lai Jan 2003 B1
6514788 Quinn Feb 2003 B2
6514820 Ahn et al. Feb 2003 B2
6534781 Dennison Mar 2003 B2
6545903 Wu Apr 2003 B1
6551866 Maeda et al. Apr 2003 B1
6555860 Lowrey et al. Apr 2003 B2
6563156 Harshfield May 2003 B2
6566700 Xu May 2003 B2
6567293 Lowrey et al. May 2003 B1
6576546 Gilbert et al. Jun 2003 B2
6579760 Lung et al. Jun 2003 B1
6586761 Lowrey Jul 2003 B2
6589714 Maimon et al. Jul 2003 B2
6593176 Dennison Jul 2003 B2
6596589 Tseng et al. Jul 2003 B2
6597009 Wicker Jul 2003 B2
6605477 Uchiyama Aug 2003 B2
6605527 Dennison et al. Aug 2003 B2
6605821 Lee et al. Aug 2003 B1
6607974 Harshfield Aug 2003 B2
6613604 Maimon et al. Sep 2003 B2
6617192 Lowrey et al. Sep 2003 B1
6621095 Chiang et al. Sep 2003 B2
6627530 Li et al. Sep 2003 B2
6639849 Takahashi et al. Oct 2003 B2
6673700 Dennison et al. Jan 2004 B2
6674115 Hudgens et al. Jan 2004 B2
6677678 Biolsi et al. Jan 2004 B2
6744088 Dennison Jun 2004 B1
6750079 Lowrey et al. Jun 2004 B2
6750101 Lung et al. Jun 2004 B2
6791102 Johnson et al. Sep 2004 B2
6797979 Chiang et al. Sep 2004 B2
6800504 Li et al. Oct 2004 B2
6805563 Ohashi Oct 2004 B2
6815704 Chen Nov 2004 B1
6830952 Lung et al. Dec 2004 B2
6838692 Lung et al. Jan 2005 B1
6850432 Lu et al. Feb 2005 B2
6859389 Idehara et al. Feb 2005 B2
6861267 Xu et al. Mar 2005 B2
6864500 Gilton Mar 2005 B2
6864503 Lung et al. Mar 2005 B2
6867638 Saiki et al. Mar 2005 B2
6881603 Lai Apr 2005 B2
6888750 Walker et al. May 2005 B2
6894304 Moore May 2005 B2
6894305 Yi et al. May 2005 B2
6900517 Tanaka et al. May 2005 B2
6903362 Wyeth et al. Jun 2005 B2
6909107 Rodgers et al. Jun 2005 B2
6910907 Layadi et al. Jun 2005 B2
6927410 Chen Aug 2005 B2
6928022 Cho et al. Aug 2005 B2
6933516 Xu Aug 2005 B2
6936544 Huang et al. Aug 2005 B2
6936840 Sun et al. Aug 2005 B2
6937507 Chen Aug 2005 B2
6943365 Lowrey et al. Sep 2005 B2
6969866 Lowrey et al. Nov 2005 B1
6972428 Maimon Dec 2005 B2
6972430 Casagrande et al. Dec 2005 B2
6977181 Raberg et al. Dec 2005 B1
6992932 Cohen et al. Jan 2006 B2
7023009 Kostylev et al. Apr 2006 B2
7029924 Hsu et al. Apr 2006 B2
7033856 Lung et al. Apr 2006 B2
7038230 Chen et al. May 2006 B2
7038938 Kang et al. May 2006 B2
7042001 Kim et al. May 2006 B2
7067864 Nishida et al. Jun 2006 B2
7067865 Lung et al. Jun 2006 B2
7078273 Matsuoka et al. Jul 2006 B2
7115927 Hideki et al. Oct 2006 B2
7122281 Pierrat Oct 2006 B2
7122824 Khouri et al. Oct 2006 B2
7126149 Iwasaki et al. Oct 2006 B2
7132675 Gilton Nov 2006 B2
7154774 Bedeschi et al. Dec 2006 B2
7164147 Lee et al. Jan 2007 B2
7166533 Happ Jan 2007 B2
7169635 Kozicki Jan 2007 B2
7202493 Lung et al. Apr 2007 B2
7208751 Ooishi et al. Apr 2007 B2
7214958 Happ May 2007 B2
7220983 Lung May 2007 B2
7229883 Wang et al. Jun 2007 B2
7238994 Chen et al. Jul 2007 B2
7248494 Oh et al. Jul 2007 B2
7251157 Osada et al. Jul 2007 B2
7253429 Klersy et al. Aug 2007 B2
7269052 Segal et al. Sep 2007 B2
7277317 Le Phan et al. Oct 2007 B2
7291556 Choi et al. Nov 2007 B2
7309630 Fan et al. Dec 2007 B2
7321130 Lung et al. Jan 2008 B2
7323708 Lee et al. Jan 2008 B2
7332370 Chang et al. Feb 2008 B2
7336526 Osada et al. Feb 2008 B2
7351648 Furukawa et al. Apr 2008 B2
7359231 Venkataraman et al. Apr 2008 B2
7364935 Lung Apr 2008 B2
7365385 Abbott Apr 2008 B2
7379328 Osada et al. May 2008 B2
7385235 Lung et al. Jun 2008 B2
7393798 Campbell Jul 2008 B2
7394088 Lung Jul 2008 B2
7397060 Lung Jul 2008 B2
7423300 Lung et al. Sep 2008 B2
7426134 Happ et al. Sep 2008 B2
7449710 Lung Nov 2008 B2
20010034078 Zahorik et al. Oct 2001 A1
20020070457 Sun et al. Jun 2002 A1
20020113273 Hwang et al. Aug 2002 A1
20030072195 Mikolajick Apr 2003 A1
20030095426 Hush et al. May 2003 A1
20030186481 Lung Oct 2003 A1
20030209746 Horii Nov 2003 A1
20030224598 Lee et al. Dec 2003 A1
20040026686 Lung Feb 2004 A1
20040051094 Ooishi Mar 2004 A1
20040165422 Hideki et al. Aug 2004 A1
20040248339 Lung Dec 2004 A1
20040256610 Lung Dec 2004 A1
20050018526 Lee Jan 2005 A1
20050029502 Hudgens Feb 2005 A1
20050037546 Yeh et al. Feb 2005 A1
20050062087 Chen et al. Mar 2005 A1
20050093022 Lung May 2005 A1
20050110983 Jeong et al. May 2005 A1
20050127349 Horak et al. Jun 2005 A1
20050145984 Chen et al. Jul 2005 A1
20050191804 Lai et al. Sep 2005 A1
20050201182 Osada et al. Sep 2005 A1
20050212024 Happ Sep 2005 A1
20050212026 Chung et al. Sep 2005 A1
20050215009 Cho Sep 2005 A1
20060006472 Jiang Jan 2006 A1
20060038221 Lee et al. Feb 2006 A1
20060054950 Baek et al. Mar 2006 A1
20060066156 Dong et al. Mar 2006 A1
20060073642 Yeh et al. Apr 2006 A1
20060091476 Pinnow et al. May 2006 A1
20060094154 Lung May 2006 A1
20060108667 Lung May 2006 A1
20060110878 Lung et al. May 2006 A1
20060110888 Cho et al. May 2006 A1
20060113521 Lung Jun 2006 A1
20060118913 Yi et al. Jun 2006 A1
20060124916 Lung Jun 2006 A1
20060126395 Chen et al. Jun 2006 A1
20060131555 Liu et al. Jun 2006 A1
20060138467 Lung Jun 2006 A1
20060154185 Ho et al. Jul 2006 A1
20060157681 Chen et al. Jul 2006 A1
20060163554 Lankhorst et al. Jul 2006 A1
20060194403 Li et al. Aug 2006 A1
20060198183 Kawahara et al. Sep 2006 A1
20060205108 Maimon et al. Sep 2006 A1
20060211165 Hwang et al. Sep 2006 A1
20060226409 Burr et al. Oct 2006 A1
20060226411 Lee Oct 2006 A1
20060234138 Fehlhaber et al. Oct 2006 A1
20060284157 Chen et al. Dec 2006 A1
20060284158 Lung et al. Dec 2006 A1
20060284214 Chen Dec 2006 A1
20060284279 Lung et al. Dec 2006 A1
20060286709 Lung et al. Dec 2006 A1
20060286743 Lung et al. Dec 2006 A1
20060286762 Tseng et al. Dec 2006 A1
20060289848 Dennison Dec 2006 A1
20070008786 Scheuerlein Jan 2007 A1
20070010054 Fan et al. Jan 2007 A1
20070030721 Segal et al. Feb 2007 A1
20070037101 Morioka Feb 2007 A1
20070072125 Sousa et al. Mar 2007 A1
20070096162 Happ et al. May 2007 A1
20070108077 Lung et al. May 2007 A1
20070108429 Lung May 2007 A1
20070108430 Lung May 2007 A1
20070108431 Chen et al. May 2007 A1
20070109836 Lung May 2007 A1
20070109843 Lung et al. May 2007 A1
20070111429 Lung May 2007 A1
20070115794 Lung May 2007 A1
20070117315 Lai et al. May 2007 A1
20070121363 Lung May 2007 A1
20070121374 Lung et al. May 2007 A1
20070126040 Lung Jun 2007 A1
20070131922 Lung Jun 2007 A1
20070138458 Lung Jun 2007 A1
20070147105 Lung et al. Jun 2007 A1
20070153563 Nirschl Jul 2007 A1
20070154847 Chen et al. Jul 2007 A1
20070155172 Lai et al. Jul 2007 A1
20070158632 Ho Jul 2007 A1
20070158633 Lai et al. Jul 2007 A1
20070158645 Lung Jul 2007 A1
20070158690 Ho et al. Jul 2007 A1
20070158862 Lung Jul 2007 A1
20070161186 Ho Jul 2007 A1
20070173019 Ho et al. Jul 2007 A1
20070173063 Lung Jul 2007 A1
20070176261 Lung Aug 2007 A1
20070187664 Happ Aug 2007 A1
20070201267 Happ et al. Aug 2007 A1
20070215852 Lung Sep 2007 A1
20070224726 Chen et al. Sep 2007 A1
20070235811 Furukawa et al. Oct 2007 A1
20070236989 Lung Oct 2007 A1
20070246699 Lung Oct 2007 A1
20070249090 Philipp et al. Oct 2007 A1
20070257300 Ho et al. Nov 2007 A1
20070262388 Ho et al. Nov 2007 A1
20070274121 Lung et al. Nov 2007 A1
20070285960 Lung et al. Dec 2007 A1
20070298535 Lung Dec 2007 A1
20080006811 Philipp et al. Jan 2008 A1
20080012000 Harshfield Jan 2008 A1
20080014676 Lung et al. Jan 2008 A1
20080025089 Scheuerlein et al. Jan 2008 A1
20080043520 Chen Feb 2008 A1
20080094871 Parkinson Apr 2008 A1
20080101110 Happ et al. May 2008 A1
20080137400 Chen et al. Jun 2008 A1
20080164453 Breitwisch et al. Jul 2008 A1
20080165569 Chen et al. Jul 2008 A1
20080165570 Happ et al. Jul 2008 A1
20080165572 Lung Jul 2008 A1
20080166875 Lung Jul 2008 A1
20080179582 Burr et al. Jul 2008 A1
20080180990 Lung Jul 2008 A1
20080186755 Lung et al. Aug 2008 A1
20080191187 Lung et al. Aug 2008 A1
20080192534 Lung Aug 2008 A1
20080197334 Lung Aug 2008 A1
20080224119 Burr et al. Sep 2008 A1
20080225489 Cai et al. Sep 2008 A1
Foreign Referenced Citations (2)
Number Date Country
WO-0079539 Dec 2000 WO
WO-0145108 Jun 2001 WO
Related Publications (1)
Number Date Country
20090148981 A1 Jun 2009 US
Provisional Applications (1)
Number Date Country
60754161 Dec 2005 US
Divisions (1)
Number Date Country
Parent 11463824 Aug 2006 US
Child 12351692 US