This application is related to U.S. patent application Ser. No. 12/353,219, entitled “Polysilicon Plug Bipolar Transistor for Phase Change Memory,”filed on 13 Jan. 2009, now U.S. Pat. No. 8,030,635.
International Business Machines Corporation, a New York corporation, and Macronix International Corporation, Ltd., a Taiwan corporation, are parties to a Joint Research Agreement.
1. Field of the Invention
The present invention relates to high density memory devices based on phase change based memory materials, including chalcogenide based materials and on other programmable resistive materials, and methods for manufacturing such devices.
2. Description of Related Art
Phase change based memory materials, like chalcogenide based materials and similar materials, can be caused to change phase between an amorphous state and a crystalline state by application of electrical current at levels suitable for implementation in integrated circuits. The generally amorphous state is characterized by higher electrical 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 phase change material cools quickly, quenching the molten phase change material and allowing at least a portion of the phase change material to stabilize in the amorphous state.
Because the phase change occurs as a result of heating, a relatively large current is needed in order to heat the phase change material and induce the desired phase change. Issues have arisen in obtaining the necessary current for phase change memory cells having field effect transistor access devices due to the relatively low current drive of field effect transistors.
Bipolar junction transistors can provide larger current drive than field effect transistors, but the integration of bipolar junction transistors with CMOS peripheral circuitry is difficult and may result in highly complex designs and manufacturing processes.
The magnitude of the current can be reduced by reducing the size of the phase change memory element in the cell, so that higher current densities are achieved with small absolute current values through the phase change memory element. However, problems have arisen in manufacturing devices with very small dimensions and with variations in manufacturing processes needed to meet the tight tolerance requirements necessary for large scale high-density memory devices.
It is therefore desirable to provide phase change memory cells with bipolar junction transistor access devices addressing the complexity of design integration with CMOS peripheral circuitry, and compatible with manufacturing of peripheral circuitry on the same integrated circuit. Furthermore, it is desirable to provide methods for manufacturing phase change memory cells addressing the tight tolerance requirements needed for large-scale high-density memory devices.
Memory cells having memory elements self-aligned with the emitters of bipolar junction transistor access devices are described herein. A memory device as described herein comprises a plurality of memory cells. Memory cells in the plurality of memory cells include a bipolar junction transistor comprising an emitter comprising a pillar of doped polysilicon. An insulating element is over the emitter and has an opening extending through the insulating element, the opening centered over the emitter. A memory element is within the opening and is electrically coupled to the emitter.
In embodiments the emitter can be formed during the formation of a sacrificial element used to define the location of the subsequently formed memory element. The sacrificial element is removed to define a via overlying the emitter and an insulating element is formed in the via. The memory element is formed within an opening defined by the insulating element. The opening defined by the insulating element can be formed by processes which result in very small variations in the sublithographic width of the memory element across an array of memory cells.
A memory cell described herein results in the active region within the memory element that can be made extremely small, thereby reducing the magnitude of the current needed to induce a phase change. The width of the memory element within the opening defined by the insulating element is less than that of the doped polysilicon pillar and conductive cap acting as the emitter, and preferably less than a minimum feature size for a process, for example a lithographic process, used to form the doped polysilicon pillar, conductive cap, and bit lines. The small width concentrates current density within the memory element, thereby reducing the magnitude of the current needed to induce a phase change in the active region. Additionally, the insulating element may provide some thermal isolation to the active region, which also helps to reduce the amount of current necessary to induce a phase change. Furthermore, the remaining portion of the memory element can provide some thermal isolation from the bit line for the active region.
A method for manufacturing a memory device described herein comprises forming a single-crystalline substrate having a first conductivity type. A plurality of dielectric trenches and a plurality of word lines are formed within the single-crystalline substrate. Adjacent word lines are separated by a dielectric trench in the plurality of dielectric trenches. A structure is formed overlying the single-crystalline substrate, the structure comprising doped polysilicon material, conductive cap material on the doped polysilicon material, and a sacrificial material on the conductive cap material. The structure is patterned to form a plurality of stacks on the word lines. Sidewall spacers are formed on sidewalls of the stacks. The sacrificial material is removed to define vias, and an insulating layer is formed within the vias, the insulating layer defining openings. Memory elements are formed within the openings, and a plurality of bit lines are formed on the memory elements.
In embodiments described herein logic devices in the periphery region and the memory cells having bipolar junction transistors in the memory region are manufactured concurrently. Gate dielectric material is formed within the memory and periphery regions. The gate dielectric material is removed from the memory region, and a layer of doped polysilicon material and a layer of conductive cap material are formed within the memory and periphery regions. The gates of the logic devices and the emitters of the bipolar junction transistor access devices are both formed using the material of the layers of doped polysilicon material and the conductive cap material. As a result, memory devices described herein include phase change memory cells with bipolar junction transistor access devices compatible with CMOS peripheral circuitry while also addressing the complexity of design integration and manufacturing processes.
Other aspects and advantages of the present invention can be seen on review of the drawings, the detailed description, and the claims which follow.
b illustrate steps in a fabrication sequence for manufacturing an array of memory cells having bipolar junction transistors with polysilicon emitters and self-aligned memory elements as described herein.
The following description of the disclosure will typically be with reference to specific structural embodiments and methods. It is to be understood that there is no intention to limit the disclosure to the specifically disclosed embodiments and methods, but that the disclosure may be practiced using other features, elements, methods and embodiments. Preferred embodiments are described to illustrate the present disclosure, 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. Like elements in various embodiments are commonly referred to with like reference numerals.
As shown in the schematic diagram of
The array 100 comprises a plurality of word lines 130 including word lines 130a, 130b, 130c, 130d extending in parallel in a first direction and in electrical communication with word line decoder/driver 150. The word lines 130 are coupled to the base terminals of the bipolar access transistors of the array 100.
A plurality of bit lines 120 including bit lines 120a, 120b, 120c, 120d extend in parallel in a second direction and are in electrical communication with bit line decoder 160. The emitter terminals of the respective bipolar junction transistors are coupled to a corresponding bit line 120 via the memory elements.
The memory cells of the array 100 are coupled in a common collector configuration. In a common collector configuration, the collector terminals of the memory cells are coupled to a constant reference voltage, and the input and output are the base and emitter terminals respectively. Thus, in operation voltages on the bit lines 120 and word lines 130 induce a current to from the bit lines 120 to the collector terminals, or vice versa, through the emitter terminals and the memory elements.
In
Memory cell 110 is representative of the memory cells of array 100 and comprises bipolar junction transistor 115 and phase change memory element 125 arranged in electrical series. The base terminal of the bipolar junction transistor 115 is coupled to the word line 130b, and the emitter terminal of the transistor 115 is coupled to the bit line 120b via the phase change memory element 125.
Reading or writing to memory cell 110 of array 100 can be achieved by applying appropriate voltages and/or currents to the corresponding word line 130b and the corresponding bit line 120b to induce a current through the selected memory cell 110. The level and duration of the voltages/currents applied is dependent upon the operation performed, e.g. a reading operation or a writing operation.
In a reset (erase) operation of the memory cell 110, a reset pulse applied to the word line 130b, and the bit line 120b induces a current through the memory element 125 to cause a transition of an active region of the memory element 125 into an amorphous phase, thereby setting the phase change material to a resistance within a resistive value range associated with the reset state. The reset pulse is a relatively high energy pulse, sufficient to raise the temperature of at least the active region of the memory element 125 above the transition (crystallization) temperature of the phase change material and also above the melting temperature to place at least the active region in a liquid state. The reset pulse is then quickly terminated, resulting in a relatively quick quenching time as the active region quickly cools to below the transition temperature so that the active region stabilizes to a generally amorphous phase.
In a set (or program) operation of memory cell 110, a program pulse is applied to the word line 130b and the bit line 120b of suitable amplitude and duration to induce a current through the memory cell 110 sufficient to raise the temperature of at least a portion of the active region above the transition temperature and cause a transition of at least a portion of the active region from the amorphous phase into a crystalline phase, this transition lowering the resistance of the memory element 125 and setting the memory cell 110 to the desired state.
In a read (or sense) operation of the data value stored in the memory cell 110, a read pulse applied to the corresponding word line 130b and the corresponding bit line 120b of suitable amplitude and duration to induce current to flow that does not result in the memory element 125 undergoing a change in resistive state. The current through the memory cell 110 is dependent upon the resistance of the memory element 125 and thus the data value stored in the memory cell 110. Thus, the data state of the memory cell may be determined, for example, by comparison of the current on bit line 120b with a suitable reference current by sense amplifiers of block 165.
The array 100 includes a memory region 280 and a periphery region 285 on a single-crystalline semiconductor substrate 200. The periphery region 285 includes logic device 286 having a gate structure 287 on a gate dielectric layer 293 and overlying the substrate 200, and doped regions 288, 289 acting as the source and drain regions. The gate structure 287 comprises a conductive cap 291 on a doped polysilicon portion 290, and a dielectric spacer 292 on the sidewall of the conductive cap 291 and doped polysilicon portion 290. The conductive cap 291 comprises a silicide containing, for example, Ti, W, Co, Ni, or Ta. A conductive plug 295 is coupled to doped region 288 and extends to the top surface of dielectric 294 to contact bit line 120b, the dielectric 294 comprising one or more layers of dielectric material. A conductive plug 296 is coupled to doped region 289 and extends to the top surface of dielectric 294 to contact line 297.
The memory region 280 includes a well 202 having a first conductivity type within substrate 200, the well 202 comprising a first doped region 205 and a second doped region 210 more highly doped than the first doped region 205. The substrate 200 also includes word lines 130 within the well 202 and extending in a first direction into and out of the cross-section illustrated in
The memory cell 110 includes a doped polysilicon pillar 220 having the first conductivity type, the doped polysilicon pillar 220 contacting the corresponding word line 130b. The doped polysilicon pillar 220 is more highly doped than the portion of the word line 130b underlying the doped polysilicon pillar 220. Thus the pillar 220 and the word line 130b define a pn junction near the interface 222 that is largely inside the word line 130b.
The memory cell 110 includes a conductive cap 240 on the doped polysilicon pillar 220. In the illustrated embodiment the conductive cap 240 comprises a silicide containing, for example, Ti, W, Co, Ni, or Ta. The conductive cap 240 provides a low resistance contact between the doped polysilicon pillar 220 and memory element 125, assists in maintaining the uniformity of current in the doped polysilicon pillar 220 during operation by providing a contact surface that is more highly conductive than the polysilicon material of pillar 220, and can be used as a protective etch stop layer for the doped polysilicon pillar 220 during selective etching of material overlying the pillar 220. In some embodiments the conductive cap 240 may be omitted.
The doped polysilicon pillar 220 and conductive cap 240 extend through dielectric 270. In the illustrated embodiment the dielectric 270 comprises boro-phospho-silicate glass (BPSG) or PSG.
As can be seen in
The doped polysilicon pillar 220 and conductive cap 240 act as the emitter of the bipolar junction transistor 115 of the memory cell 110. A portion of the word line 130b underlying the pillar 220 acts as the base of the bipolar junction transistor 115 of the memory cell 110. A portion of the well underlying the word line 130b acts as a collector of the bipolar junction transistor 115 of the memory cell 110.
Conductive contacts 215 couple the second doped region 210 of the well 202 to the conductive material 140 coupled to a reference voltage.
In the illustrated embodiment the doped polysilicon pillar 220 comprises highly doped N-type (N++) polysilicon, the word lines 130 comprise regions of doped P-type material in substrate 200, the first doped region 205 comprises regions of doped N-type material in substrate 200, and the second doped region 210 comprises regions of highly doped N-type (N+) material in substrate 200, thus forming npn bipolar transistor 115.
In an alternative embodiment the doped polysilicon pillar 220 comprises highly doped P-type (P++) polysilicon, the word lines 130 comprise regions of doped N-type material in substrate 200, the first doped region 205 comprises regions of doped P-type material in substrate 200, and the second doped region 210 comprises regions of highly doped P-type (P+) material in substrate 200, thus forming pnp bipolar transistor 115.
Memory element 125 is within an opening defined by a insulating element 245 and electrically couples the conductive cap 240 to the bit line 120b. As a result, the memory element 125 has a bottom surface with a surface area less than that of the top surface of the emitter. The memory element 125 may comprise, for example, one or more materials from the group of Ge, Sb, Te, Se, In, Ti, Ga, Bi, Sn, Cu, Pd, Pb, Ag, S, Si, O, P, As, N and Au.
The insulating element 245 preferably comprises material resistant to diffusion of the memory material of memory element 160. In some embodiments the material of insulating element 245 is chosen for low thermal conductivity for reasons discussed in more detail below.
The bit lines 120, including bit line 120b acting as a top electrode for the memory cell 110, extend into and out of the cross-section illustrated in
Advantages of having both layers for the bit lines 120 include choosing the material of the first conductive layer for compatibility with the material of memory element 125, while material of the second conductive layer can be chosen for other advantages such as higher electrical conductivity than the material of the first conductive layer. In the illustrated embodiment the first conductive layer comprises TiN and the second conductive layer comprises Al. TiN may be preferred for the first conductive layer in embodiments in which the memory element 120 comprises GST (discussed below) because it makes good contact with GST, it is a common material used in semiconductor manufacturing, and it provides a good diffusion barrier. Alternatively, the first conductive layer may be TaN, TiAlN or TaAlN.
As further examples, the first and second conductive layer of the bit lines 120 may each comprise one or more elements selected from the group consisting of Ti, W, Mo, Al, Ta, Cu, Pt, Ir, La, Ni, N, O, and Ru and combinations thereof
In the illustrated embodiment the conductive material 140 and the line 297 also comprise first and second conductive layers like that of the bit lines 120. Alternatively, the conductive material 140 and line 297 may each comprise one or more layers of material each comprising, for example, one or more elements discussed above with reference to the bit lines 120.
The insulating element 245 has sides 246 vertically aligned with sides 221 of the emitter (doped polysilicon pillar 220 and conductive cap 210) to define sidewall 262, and a sidewall spacer 260 comprising dielectric material is on the sidewall 262 and surrounds the emitter and the insulating element 245.
The sides 221 of the emitter, when projected above the emitter, define a cylinder over the emitter. In the illustrated embodiment of
In the cross-sectional views illustrated in
Also described in more detail below with reference to
In operation, voltages on the bit line 120b, and word line 130b can induce a current to flow from the emitter through the memory cell 110 to the collector.
The active region 128 is the region of the memory element 125 in which the memory material is induced to change between at least two solid phases. As can be appreciated, the active region 128 can be made extremely small in the illustrated structure, thereby reducing the magnitude of the current needed to induce a phase change. The width 129 of the memory element 125 within the opening defined by the insulating element 245 is less than that of the doped polysilicon pillar 220 and conductive cap 240, and preferably less than a minimum feature size for a process, for example a lithographic process, used to form the doped polysilicon pillar 220, conductive cap 240, and bit lines 120. The small width 129 concentrates current density within the memory element 125, thereby reducing the magnitude of the current needed to induce a phase change in the active region 128. Additionally, the insulating element 245 may provide some thermal isolation to the active region 128, which also helps to reduce the amount of current necessary to induce a phase change. Furthermore, the remaining portion of the memory element 125 can provide some thermal isolation from the bit line 120b for the active region 128.
As described above, bipolar junction transistors can provide larger current drive than field effect transistors. Additionally, since the emitters of the transistors comprise doped polysilicon material a relatively large current gain can be obtained, which reduces the amount of current needed on the word lines 130 to induce the phase change in the memory elements. The reduced amount of current on the word lines 130 reduces the cross-talk between devices sharing the same word line, thus improving the performance of the array. The reduced current on the word lines 130 will also prevent parasitic BJT behavior in which the emitter of a neighboring memory cell acts as a collector.
Embodiments of the memory cells described herein include phase change based memory materials, including chalcogenide based materials and other materials, for the memory element. Chalcogens include any of the four elements oxygen (O), sulfur (S), selenium (Se), and tellurium (Te), forming part of group VIA 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 group IVA 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). Many phase change 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 U.S. Pat. No. 5,687,112 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 phase change 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.
Chalcogenides and other phase change materials are doped with impurities in some embodiments to modify conductivity, transition temperature, melting temperature, and other properties of memory elements using the doped chalcogenides. Representative impurities used for doping chalcogenides include nitrogen, silicon, oxygen, silicon dioxide, silicon nitride, copper, silver, gold, aluminum, aluminum oxide, tantalum, tantalum oxide, tantalum nitride, titanium and titanium oxide. See, e.g., U.S. Pat. No. 6,800,504, and U.S. Patent Application Publication No. U.S. 2005/0029502.
Phase change 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, phase change 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.
Phase change 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 phase change material to a generally amorphous state. A longer, lower amplitude pulse tends to change the phase change 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 phase change alloy. In following sections of the disclosure, the phase change material is referred to as GST, and it will be understood that other types of phase change 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, including other materials that use different crystal phase changes to determine resistance, or other memory materials that use an electrical pulse to change the resistance state. Examples include materials for use in resistance random access memory (RRAM) such as metal-oxides including tungsten-oxide (WOx), NiO, Nb2O5, CuO2, Ta2O5, Al2O3, CoO, Fe2O3, HfO2, TiO2, SrTiO3, (BaSr)TiO3. Additional examples include materials for use in magnetoresistance random access memory (MRAM) such as spin-torque-transfer (STT) MRAM, for example at least one of CoFeB, Fe, Co, Ni, Gd, Dy, CoFe, NiFe, MnAs, MnBi, MnSb, CrO2, MnOFe2O3, FeOFe2O5, NiOFe2O3, MgOFe2, EuO, and Y3Fe5O12. See, for example, US Publication No 2007/0176251 entitled “Magnetic Memory Device and Method of Fabricating the Same”, which is incorporated by reference herein. Additional examples include solid electrolyte materials used for programmable-metallization-cell (PMC) memory, or nano-ionic memory, such as silver-doped germanium sulfide electrolytes and copper-doped germanium sulfide electrolytes. See, for example, N. E. Gilbert et al., “A macro model of programmable metallization cell devices,” Solid-State Electronics 49 (2005) 1813-1819, which is incorporated by reference herein.
An exemplary method for forming chalcogenide material uses PVD-sputtering or magnetron-sputtering method with source gas(es) of Ar, N2, and/or He, etc. at the pressure of 1 mTorr˜100 mTorr. The deposition is usually done at room temperature. A collimator with an aspect ratio of 1˜5 can be used to improve the fill-in performance. To improve the fill-in performance, a DC bias of several tens of volts to several hundreds of volts is also used. On the other hand, the combination of DC bias and the collimater can be used simultaneously. An exemplary method for forming chalcogenide material using chemical vapor deposition (CVD) is disclosed in US Publication No 2006/0172067 entitled “Chemical Vapor Deposition of Chalcogenide Materials”, which is incorporated by reference herein. Another exemplary method for forming chalcogenide material using CVD is disclosed in Lee, et al., “Highly Scalable Phase Change Memory with CVD GeSbTe for Sub 50 nm Generation, 2007 Symposium on VLSI Technology Digest of Technical Papers, pp. 102-103.
A post-deposition annealing treatment in a vacuum or in an N2 ambient is optionally performed to improve the crystallize state of chalcogenide material. The annealing temperature typically ranges from 100° C. to 400° C. with an anneal time of less than 30 minutes.
Next, word lines 130 are formed by implantation within the first doped region 205 of the well, resulting in the structure illustrated in the cross-sectional views of
Next, gate dielectric layer 293 is formed on the structure illustrated in
Next, the dielectric layer 293 is removed from the memory region 280 of the structure illustrated in
Next, the logic device 286 is formed within the periphery region 285 of the structure illustrated in
Next, a layer 900 of dielectric material is formed on the structure illustrated in
Next, layers 900, 700, and 710 within the memory region 280 of
As can be seen in
In the illustrated embodiment the multi-layer stacks 1000 have a circular cross-section. Alternatively, in embodiments the multi-layer stacks 1000 may have a cross-section that is square, elliptical, rectangular, or somewhat irregularly shaped, depending on the manufacturing technique used to form the multi-layer stacks 1000.
Next, sidewall spacers 260 comprising dielectric material are formed on the sidewalls of the multi-layer stacks 1000, an implantation process is performed to form more highly doped regions of the portions of the word lines 130 between adjacent spacers 260, and top conductors 300 comprising self-aligned silicide (salicide) are formed on the more highly doped regions of the word lines 130, resulting in the structure illustrated in
The sidewall spacers 260 can be formed by depositing a conformal layer of sidewall spacer material on the structure illustrated in
In one embodiment the top conductors 300 comprise cobalt silicide (CoSi) and are formed by depositing a layer of cobalt and performing a rapid thermal process (RTP) such that the cobalt reacts with the silicon of the word lines 130 to form the top conductors. It is understood that other silicides may also be formed in this manner by deposition of titanium, arsenic, doped nickel, or alloys thereof, in a manner similar to the example described herein using cobalt.
Next, dielectric layer 270 is formed on the structure illustrated in
Next, an array of conductive contacts 215 are formed through the dielectric 260 to contact the second doped region 210 of the well and conductive pillars 295, 296 are formed to contact doped regions 288 and 289 respectively, resulting in the structure illustrated in
Next, the sacrificial elements 1010 of
Next, insulating elements 245 are formed within the vias 1400 of
The insulating elements 245 may be formed by forming an insulating dielectric material layer on the structure illustrated in
The insulating elements 245 may alternatively be formed by forming a material layer on the top surface of the dielectric 270 and having openings overlying the vias 1400. A selective undercutting etch is then performed on the vias 1400 such that the spacers 260 are etched while leaving the material layer on the top surface of the dielectric 270 intact. Insulating layer material is in then formed in the via 1400, which due to the selective undercutting etch process results in a self-aligned void in the insulating layer material being formed within the via 1400. Next, an anisotropic etching process is performed on the insulating layer material to open the void, and etching continues until a portion of the top surface of the conductive cap 240 is exposed in the region below the void, thereby forming the insulating element 245 comprising insulating layer material within the void 1400.
Next, the memory elements 125 are formed within the openings 1510 defined by the insulating elements 245 of the structure illustrated in
Next, the bit lines 120, conductive material 140 coupled to a reference voltage, and line 297 are formed on the structure illustrated in
As described above, the doped polysilicon pillars 220 and conductive caps 240 are formed during the formation of sacrificial elements 1010 which define the locations of the subsequently formed insulating elements 245 and memory elements 125. The spacers 260 are then formed and the sacrificial elements 1010 are selectively removed to form vias 1400 defined by the spacers 260 and overlying the conductive caps 240. The insulating elements 245 are then formed within the vias 1400 and have openings centered within the cylinder defined by the sides of the emitter, and the memory element 125 is formed within an opening 1510 defined by the insulating element 245. Thus, the memory elements are centered on and self-aligned to the doped polysilicon pillars 220 and the conductive caps 240, the doped polysilicon pillars 220 and conductive caps 240 acting as the emitters of the bipolar junction transistors of the memory cells.
Since the logic devices in the periphery region and the memory cells having bipolar junction transistors in the memory region are manufactured concurrently in the manufacturing steps described, the memory device has a reduced complexity and addresses the compatibility of design integration issues discussed above, thereby reducing the cost. As described above, bipolar junction transistors can provide larger current drive than field effect transistors. Additionally, since the emitters of the transistors comprise doped polysilicon material a relatively large current gain can be obtained, which reduces the amount of current needed on the word lines 130 to induce the phase change in the memory elements. The reduced amount of current on the word lines 130 reduces the cross-talk between devices sharing the same word line, thus improving the performance of the array.
As illustrated in the cross-sectional view of
Next, sidewall conductors 1900 are formed on the exposed sidewall surfaces 1800 of the first doped region 205 of the well of
Next, dielectric material is formed on the structure illustrated in
Next, ion implantation is performed to implant dopants to form word lines 130, the word lines 130 having a conductivity type opposite that of the first and second doped regions 205 and 210 of the well and resulting in the structure illustrated in the cross-sectional view of
A controller 2234 implemented in this example, using a bias arrangement state machine, controls the application of bias arrangement supply voltages and current sources 2236, such as read, program, erase, erase verify and program verify voltages and/or currents. Controller 2234 may be implemented using special-purpose logic circuitry as known in the art. In alternative embodiments, controller 2234 comprises a general-purpose processor, which may be implemented on the same integrated circuit to execute a computer program to control the operations of the device. In yet other embodiments, a combination of special-purpose logic circuitry and a general-purpose processor may be utilized for implementation of controller 2234.
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.
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 |
5751012 | Wolstenholme et al. | May 1998 | A |
5754472 | Sim et al. | May 1998 | A |
5789277 | Zahorik et al. | Aug 1998 | A |
5789758 | Reinberg | Aug 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 |
6075719 | Lowrey et al. | Jun 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 |
6337266 | Zahorik | Jan 2002 | 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 |
6429065 | Forbes | Aug 2002 | B2 |
6440837 | Harshfield | Aug 2002 | B1 |
6462353 | Gilgen | Oct 2002 | B1 |
6483736 | Johnson et al. | Nov 2002 | B2 |
6487106 | Kozicki | Nov 2002 | B1 |
6487114 | Jong et al. | Nov 2002 | B2 |
6501111 | Lowrey | Dec 2002 | B1 |
6511867 | Lowrey et al. | Jan 2003 | B2 |
6512241 | Lai | Jan 2003 | B1 |
6512263 | Yuan et al. | 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 | 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 |
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 |
6800563 | Xu | Oct 2004 | B2 |
6815704 | Chen | Nov 2004 | B1 |
6838692 | Lung et al. | Jan 2005 | B1 |
6850432 | Lu et al. | Feb 2005 | B2 |
6859389 | Idehara | 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 |
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 |
7054183 | Rinerson et al. | May 2006 | B2 |
7067837 | Hwang et al. | Jun 2006 | B2 |
7067864 | Nishida et al. | Jun 2006 | B2 |
7067865 | Lung et al. | Jun 2006 | B2 |
7078273 | Matsuoka et al. | Jul 2006 | B2 |
7099180 | Dodge et al. | Aug 2006 | B1 |
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 |
7126847 | Ha et al. | Oct 2006 | B2 |
7132675 | Gilton | Nov 2006 | B2 |
7151273 | Campbell et al. | Dec 2006 | B2 |
7154774 | Bedeschi et al. | Dec 2006 | B2 |
7158411 | Yeh et al. | Jan 2007 | 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 |
7238959 | Chen | Jul 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 |
7254059 | Li 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 |
7323734 | Ha 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 et al. | Apr 2008 | B2 |
7365385 | Abbott | Apr 2008 | B2 |
7379328 | Osada et al. | May 2008 | B2 |
7385235 | Lung et al. | Jun 2008 | B2 |
7388273 | Burr et al. | Jun 2008 | B2 |
7394088 | Lung | Jul 2008 | B2 |
7397060 | Lung | Jul 2008 | B2 |
7400522 | Toda et al. | Jul 2008 | B2 |
7423300 | Lung et al. | Sep 2008 | B2 |
7426134 | Happ et al. | Sep 2008 | B2 |
7440308 | Jeong et al. | Oct 2008 | B2 |
7449710 | Lung | Nov 2008 | B2 |
7473576 | Lung | Jan 2009 | B2 |
7479649 | Lung | Jan 2009 | B2 |
7485891 | Hamann et al. | Feb 2009 | B2 |
7502252 | Fuji et al. | Mar 2009 | B2 |
7507986 | Lung | Mar 2009 | B2 |
7514334 | Chen et al. | Apr 2009 | B2 |
7514705 | Breitwisch et al. | Apr 2009 | B2 |
7515461 | Happ et al. | Apr 2009 | B2 |
7651906 | Park et al. | Jan 2010 | B2 |
7858960 | Chang | Dec 2010 | B2 |
8369139 | Liu et al. | Feb 2013 | B2 |
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 |
20040026686 | Lung | Feb 2004 | A1 |
20040051094 | Ooishi | Mar 2004 | A1 |
20040113137 | Lowrey | Jun 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 |
20050029587 | Harshfield | Feb 2005 | A1 |
20050052904 | Cho et al. | Mar 2005 | A1 |
20050062087 | Chen et al. | Mar 2005 | A1 |
20050093022 | Lung | May 2005 | A1 |
20050127349 | Horak et al. | Jun 2005 | A1 |
20050141261 | Ahn | Jun 2005 | A1 |
20050145984 | Chen et al. | Jul 2005 | A1 |
20050167656 | Sun et al. | Aug 2005 | A1 |
20050191804 | Lai et al. | Sep 2005 | A1 |
20050195633 | Choi 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 |
20050263829 | Song et al. | Dec 2005 | A1 |
20050270832 | Chu et al. | Dec 2005 | A1 |
20060006472 | Jiang | Jan 2006 | A1 |
20060038221 | Lee et al. | Feb 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 |
20060113520 | Yamamoto et al. | Jun 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 |
20060172067 | Ovshinsky et al. | Aug 2006 | A1 |
20060175599 | Happ | Aug 2006 | A1 |
20060186483 | Cho | 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 |
20060234138 | Fehlhaber et al. | Oct 2006 | A1 |
20060237756 | Park et al. | Oct 2006 | A1 |
20060245236 | Zaidi | Nov 2006 | A1 |
20060250885 | Cho et al. | Nov 2006 | A1 |
20060261392 | Lee et al. | Nov 2006 | A1 |
20060266993 | Suh et al. | Nov 2006 | A1 |
20060284157 | Chen et al. | Dec 2006 | A1 |
20060284158 | Lung et al. | Dec 2006 | A1 |
20060284214 | Chen | Dec 2006 | A1 |
20060284237 | Park et al. | Dec 2006 | A1 |
20060284279 | Lung et al. | Dec 2006 | A1 |
20060286709 | Lung et al. | Dec 2006 | A1 |
20060286743 | Lung et al. | Dec 2006 | A1 |
20060289847 | Dodge | Dec 2006 | A1 |
20060289848 | Dennison | Dec 2006 | A1 |
20070007613 | Wang et al. | Jan 2007 | A1 |
20070008786 | Scheuerlein | Jan 2007 | A1 |
20070030721 | Segal et al. | Feb 2007 | A1 |
20070037101 | Morioka | Feb 2007 | A1 |
20070040159 | Wang | Feb 2007 | A1 |
20070096162 | Happ et al. | May 2007 | A1 |
20070096248 | Philipp et al. | May 2007 | A1 |
20070103963 | Kim 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 |
20070120104 | Ahn 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 |
20070156949 | Rudelic 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 |
20070170881 | Noh et al. | Jul 2007 | A1 |
20070173019 | Ho et al. | Jul 2007 | A1 |
20070173063 | Lung | Jul 2007 | A1 |
20070176251 | Oh et al. | Aug 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 |
20070267618 | Zaidi 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 |
20080138929 | Lung | Jun 2008 | A1 |
20080138930 | Lung | Jun 2008 | A1 |
20080138931 | Lung | 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 |
20080265234 | Breitwisch et al. | Oct 2008 | A1 |
20090001341 | Breitwisch et al. | Jan 2009 | A1 |
20090014704 | Chen et al. | Jan 2009 | A1 |
20090023242 | Lung | Jan 2009 | A1 |
20090027950 | Lam et al. | Jan 2009 | A1 |
20090042335 | Lung | Feb 2009 | A1 |
20090057641 | Lung | Mar 2009 | A1 |
20090098678 | Lung | Apr 2009 | A1 |
20090166600 | Park et al. | Jul 2009 | A1 |
20090166603 | Lung | Jul 2009 | A1 |
Entry |
---|
“Magnetic Bit Boost,” www.sciencenews.org, Dec. 18 & 25, 2004, p. 389, vol. 166. |
“New Memories Tap Spin, Gird for Battle,” Science News, Apr. 3, 1999, p. 223, vol. 155. |
“Optimized Thermal Capacitance in a Phase Change Memory Cell Design,” IPCOM000141986D, IP.com Prior Art Database, Oct. 18, 2006, 4pp. |
“Remembering on the Cheap,” www.sciencenews.org, Mar. 19, 2005, p. 189, vol. 167. |
“Thermal Conductivity of Crystalline Dielectrics” in CRC Handbook of Chemistry and Physics, Internet Version 2007, (87th edition), David R. Lide, ed. Taylor and Francis, Boca Raton, Fl, 2pp. |
Adler, D. et al., “Threshold Switching in Chalcogenide-Glass Thin Films,” J. Appl/Phys 51(6), Jun. 1980, pp. 3289-3309. |
Adler, David, “Amorphous-Semiconductor Devices,” Sci. Amer., vol. 236, pp. 36-48, May 1977. |
Ahn, S. J. et al., “A Highly Manufacturable High Density Phase Change Memory of 64 Mb and Beyond,” IEEE IEDM 2004, pp. 907-910. |
Ahn, S. J. et al., “Highly Reliable 5nm Contact Cell Technology for 256Mb PRAM,” VLSI Technology, Digest of Technical Papers, Jun. 14-16, 2005, pp. 98-99. |
Atwood, G, et al., “90 nm Phase Change Technology with u Trench and Lance Cell Elements,” VLSI Technology, Systems and Applications, Apr. 23-25, 2007, pp. 1-2. |
Axon Technologies Corporation paper: Technology Description, published in 1997, pp. 1-6. |
Bedeschi, F. et al., “4-MB MOSFET-Selected Phase-Change Memory Experimental Chip,” IEEE, 2004, 4 PP. |
Blake thesis, “Investigation of GeTeSb5 Chalcogenide Films for Use as an Analog Memory,” AFIT/GE/ENG/00M-04, Mar. 2000, 121 pages. |
Chao, Der-Sheng, et al., “Low Programming Current Phase Change Memory Cell with Double GST Thermally Confined Structure,” Int'l Symp on VLSI Technology, Systems and Applications, Apr. 23-25, 2007, pp. 1-2. |
Chen, An et al., “Non-Volatile Resistive Switching for Advanced Memory Applications,” IEEE IEDM, Dec. 5-7, 2005, 4 pp. |
Cho, S. L. et al., “Highly Scalable On-axis Confined Cell Structure for High Density PRAM beyond 256Mb,” 2005 Symposium on VLSI Technology Digest of Technical Papers, pp. 96-97. |
Gibson, G. A. et al., “Phase-change Recording Medium that Enables Ultrahigh-density Electron-beam Data Storage,” Applied Physics Letter, 2005, 3 pp., vol. 86. |
Gilbert, N.E., “A macro model of programmable metallization cell devices,” Solid-State Electronics 49 (2005) 1813-1819. |
Gill, Manzur et al., “A High-Performance Nonvolatile Memory Technology for Stand-Alone Memory and Embedded Applications,” 2002 IEEE-ISSCC Technical Digest (TD 12.4), 7 pp. |
Gleixner, “Phase Change Memory Reliability”, 22nd NVSMW, Aug. 26, 2007, 46 pages. |
Ha, Y. H. et al., “An Edge Contact Type Cell for Phase Change RAM Featuring Very Low Power Consumption,” 2003 Symposium on VLSI Technology Digest of Technical Papers, pp. 175-176. |
Hanzawa, Satoru, et al., “A 512kB Embedded Phase Change Memory with 416kB/s Write Throughput at 100μA Cell Write Current,” ISSCC 2007, Session 26, Non-Volatile Memories/26.2, 3 pages. |
Happ, T. D. et al., “Novel None-Mask Self-Heating Pillar Phase Change Memory,” 2006 Symposium on VLSI Technology, 2 pp. |
Haring Bolivar, P. et al., “Lateral Design for Phase Change Random Access Memory Cells with Low-Current Consumption,” presented at 3rd E*PCOS 04 Symposium in Balzers, Principality of Liechtenstein, Sep. 4-7, 2004, 4pp. |
Horii, H. et al., “A Novel Cell Technology Using N-doped GeSbTe Films for Phase Change RAM,” 2003 Symposium on VLSI Technology Digest of Technical Papers, pp. 177-178. |
Hudgens, S. et al., “Overview of Phase-Change Chalcogenide Nonvolatile Memory Technology,” MRS Bulletin, Nov. 2004, pp. 829-832. |
Hwang, Y. N. et al., “Full Integration and Reliability Evaluation of Phase-change RAM Based on 0.24um-CMOS Technologies,” 2003 Symposium on VLSI Technology Digest of Technical Papers, pp. 173-174. |
Iwasaki, Hiroko et al., “Completely Erasable Phase Change Optical Disk,” Jpn. J. Appl. Phys., Feb. 1992, pp. 461-465, vol. 31. |
Jeong, C. W. et al., “Switching Current Scaling and Reliability Evaluation in PRAM,” IEEE Non-Volatile Semiconductor Memory Workshop, Monterey, CA 2004, pp. 28-29 and workshop cover sheet. |
Kim, Kinam et al., “Reliability Investigations for Manufacturable High Density PRAM,” IEEE 43rd Annual International Reliability Physics Symposium, San Jose, 2005, pp. 157-162. |
Kojima, Rie et al., “Ge—Sn—Sb—Te Phase-change Recording Material Having High Crystallization Speed,” Proceedings of PCOS 2000, pp. 36-41. |
Lacita, A. L., “Electrothermal and Phase-change Dynamics in Chalcogenide-based Memories,” IEEE IEDM 2004, 4 pp. |
Lai, Stefan, “Current Status of the Phase Change Memory and Its Future,” IEEE IEDM 2003, pp. 255-258. |
Lai, Stephan et al., “OUM-A 180 nm Nonvolatile Memory Cell Element Technology for Stand Alone and Embedded Applications,” IEEE IEDM 2001, pp. 803-806. |
Lankhorst, Martijn H.R., et al; Low-Cost and Nanoscale Non-Volatile Memory Concept for Future Silicon Chips, Mar. 13, 2005, 6 pp., Nature Materials Advance Online Publication, www.nature.com/naturematerials. |
Lee, J.I., et al., “Highly Scalable Phase Change Memory with CVD GeSbTe for Sub 50nm Genreation,” 2007 Symp on VLSI Tech. Digest of Technical Papers, pp. 102-103. |
Mott, Nevill, “Electrons in Glass,” Nobel Lecture, Dec. 8, 1977, Physics, 1977, pp. 403-413. |
Oh, Hyung-Rok, et al., “Enhanced Write Performance of a 64Mb Phase-Change Random Access Memory,” ISSCC 2005, Session 2, Non-Volatile Memory, 2.3, 3 pages. |
Oh, J.H., et al. “Full Integration of Highly Manufacturable 512Mb PRAM based on 90nm Technology,” International Electron Devices Meeting, 2006. Dec. 11-13, 2006 pp. 1-4. |
Ovonyx Non-Confidential paper entitled “Ovonic Unified Memory,” Dec. 1999, pp. 1-80. |
Ovshinsky, Sandford R., “Reversible Electrical Switching Phenomena in Disordered Structures,” Physical Review Letters, vol. 21, No. 20, Nov. 11, 1968, pp. 1450-1453. |
Owen, Alan E. et al., “Electronic Conduction and Switching in Chalcogenide Glasses,” IEEE Transactions on Electron Devices, vol. Ed. 20, No. 2, Feb. 1973, pp. 105-122. |
Pellizer, F. et al.,“Novel u Trench Phase-Change Memory Cell for Embedded and Stand-Alone Non-Volatile Memory Applications,” 2004 Symposium on VLSI Technology Digest of Technical Papers, pp. 18-19. |
Pirovano, Agostino et al.,“Reliability Study of Phase-Change Nonvolatile Memories,” IEEE Transactions on Device and Materials Reliability, Sep. 2004, pp. 422-427, vol. 4, No. 3. |
Prakash, S. et al., “A guideline for Designing Chalcogenide-Based Glasses for Threshold Switching Characteristics,” IEEE Electron Device Letters, vol. 18, No. 2, Feb. 1997, pp. 45-47. |
Radaelli, A. et al., “Electronic Switching Effect and Phase-Change Transition in Chalcogenide Materials,” IEEE Electron Device Letters, Oct. 2004, pp. 684-686, vol. 25, No. 10. |
Rochefort, C. et al., “Manufacturing of High Aspect-Ration p-n Junctions Using Vapor Phase Doping for Application in Multi-Resurf Devices,” IEEE 2002, pp. 237-240. |
Schafft, Harry A. et al., “Thermal Conductivity Measurements of Thin Films Silicon Dioxide,” Proceedings of the IEEE 1989 International Conference on Microelectronic Test Structures vol. 2, No. 1, Mar. 1989, pp. 121-124. |
Strauss, Karl F. et al., “Overview of Radiation Tolerant Unlimited Write Cycle Non-Volatile Memory,” IEEE 2000, pp. 399-408. |
Subramanian, Vivek et al., “Low Leakage Germanium-Seeded Laterally-Crystallized Single-Grain 100-nm TFT's for Vertical Integration Applications,” IEEE Electron Device Letters, vol. 20, No. 7, Jul. 1999, pp. 341-343. |
Wicker, Guy et al., Nonvolatile, High Density, High Performance Phase Change Memory, 1999, http://klabs.org/richcontent/MAPLDCon99/Papers/P21—Tyson—P.PDF#search=‘nonvolatile%20 high%20density%20high%20performance%20phase%20change%20memory’, 8pages. |
Wicker, Guy, “A Comprehensive Model of Submicron Chalcogenide Switching Devices,” Doctoral Dissertation, Wayne State University, Detroit, MI 1996, 137 pp. |
Wolf, Stanley, Excerpt from: Silicon Processing for the VLSI Era—vol. 4, pp. 674-679, 2004. |
Wuttig, Matthias, “Towards a Universal Memory?” Nature Materials, Apr. 2005, pp. 265-266, vol. 4. |
Yamada, Noboru, “Potential of Ge—Sb—Te phase-change optical disks for high-data-rate recording in the near future,” (Conference Proceedings Paper), Jul. 30, 1997, vol. 3109, 10 pages. |
Yi, J. H. et al., “Novel Cell Structure of PRAM with Thin Metal Layer Inserted GeSbTe,” IEEE IEDM 2003, 4 pages. |
Yonehara, T. et al., “Control of Grain Boundary Location by Selective Nucleation Over Amorphous Substrates, ” Mat. Res. Soc. Symp. Proc., vol. 106, 1998, pp. 21-26. |
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20100181649 A1 | Jul 2010 | US |