The present invention relates to monolithic techniques for integrating CMOS integrated circuit devices and solid state resistive devices used for memory storage. More particularly, some embodiments of the present invention provide methods and resulting devices including resistive memory devices and/or integrated circuits using standard IC foundry-compatible processes. Merely by way of example, embodiments of the invention can be applied to logic devices, PLD, processors, controllers, memories, and the like.
Resistive random-access memories (RRAMs) have generated significant interest recently as a potential candidate for ultra-high density non-volatile information storage. A typical RRAM device has an insulator layer provided between a pair of electrodes and exhibits electrical pulse induced hysteretic resistance switching effects.
The resistance switching has been explained by the formation of conductive filaments inside the insulator due to Joule heating and electrochemical processes in binary oxides (e.g. NiO and TiO2) or redox processes for ionic conductors including oxides, chalcogenides and polymers. Resistance switching has also been explained by field assisted diffusion of ions in TiO2 and amorphous silicon (a-Si) films.
In the case of a-Si structures, voltage-induced diffusion of metal ions into the silicon leads to the formation of conductive filaments that reduce the resistance of the a-Si structure. These filaments remain after the biasing voltage is removed, thereby giving the device its non-volatile characteristic, and they can be removed by reverse flow of the ions back toward the metal electrode under the motive force of a reverse polarity applied voltage.
Resistive devices formed by an a-Si structure provided between two metal electrodes have been shown to exhibit this controllable resistive characteristic. However, such devices typically have micron sized filaments which may prevent them from being scaled down to the sub-100 nanometer range. Such devices may also require high forming voltages that can lead to device damage and can limit production yields.
The present invention relates to solid state resistive devices used for memory storage. More particularly, the present invention relates to integrating a resistive random access memory on top of an IC substrate monolithically using IC-foundry compatible processes (e.g. a CMOS compatible backend process). In various embodiments, the IC substrate is completed first using standard IC processes. An insulating layer, e.g. dielectric, oxide layer is then added on top of the IC substrate. Subsequent CMOS compatible processes then define a solid-state resistive device. In some embodiments, the solid-state resistive device may be formed using standing CMOS processes from a semiconductor foundry.
In an embodiment, a monolithic integrated circuit and resistive memory device is disclosed. An integrated circuit (IC) substrate is provided having one or more electronic devices formed upon a substrate. The electronic devices may include transistors. On top of the IC substrate, memory devices having a crossbar array structure are formed thereon using CMOS-compatible processes, i.e. IC foundry compatible processes. In various embodiments, the memory device comprises a first array of first electrodes extending along a first direction; a second array of second electrodes extending along a second direction, each second electrode having a polycrystalline semiconductor layer including silicon; a non-crystalline silicon structure provided between the first electrode and the second electrode at an intersection defined by the first array and the second array. Each intersection of the first array and the second array defines a two-terminal resistive memory cell. In some embodiments, the IC substrate may be formed at the same foundry as the foundry that forms the two-terminal resistive memory cell. In other embodiments, the IC substrate may be formed at a first semiconductor foundry, and the two-terminal resistive memory cell may be formed on top of the IC substrate at a second semiconductor foundry.
In another embodiment, the monolithic integrated circuit includes a resistive memory device where the non-crystalline silicon structure includes amorphous silicon, and the polycrystalline semiconductor layer includes a polycrystalline silicon-germanium.
In another embodiment, the monolithic integrated circuit includes a resistive memory device that includes a first electrode; a second electrode having a polycrystalline semiconductor layer that includes silicon; a noncrystalline silicon structure provided between the first electrode and the second electrode. The first electrode, second electrode and non-crystalline silicon structure define a two-terminal resistive memory cell.
In yet another embodiment, a method for fabricating a monolithic integrated circuit and resistive memory device includes the following steps. The method includes providing a first semiconductor substrate having a first surface region and forming one or more CMOS integrated circuit devices, e.g. transistors, logic, etc., overlying the first surface region. The CMOS integrated circuit device region has a CMOS surface region. A dielectric layer is formed overlying the CMOS surface region. The method includes: forming a bottom electrode over the CMOS surface region, the bottom electrode including a polycrystalline semiconductor layer that includes silicon; forming a switching medium over the bottom electrode, the switching medium defining a region wherein a filament is to be formed when a program voltage is applied; and forming a top electrode over the switching medium, the top electrode configured to provide at least part of metal particles needed to form the filament in the region defined in the switching medium. Interconnections may be formed between one or more CMOS integrated circuit devices and the top electrode and/or the bottom electrode. Using this architecture and fabrication flow, it is feasible and cost-effective to make an array of resistive memory devices on a single CMOS chip.
The details of one or more embodiments are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.
As used herein, the term “nanoscale” or “nanostructure” refers to a structure having at least one dimension in the nanoscale range; for example, structures having a diameter or plural cross-sectional dimensions within the general range of 0.1 to 200 nanometers. This includes structures having all three spatial dimensions in the nanoscale; for example, a cylindrical nanocolumn or nanopillar having a length that is on the same order as its nanoscale diameter. Nanostructures can include the various nanoscale structures known to those skilled in the art; for example, nanotubes, nanowires, nanorods, nanocolumns, nanopillars, nanoparticles, and nanofibers.
Exemplary embodiments will hereinafter be described in conjunction with the appended drawings, wherein like designations denote like elements, and wherein:
RRAM is a two terminal memory having a switching medium provided between top and bottom electrodes. The resistance of the switching medium can be controlled by applying electrical signal to the electrodes. The electrical signal may be current-based or voltage-based. As used herein, the term “RRAM” or “resistive memory device” refers to a memory device (or memory cell) that uses a switching medium whose resistance can be controlled by applying electrical signal without ferro electricity, magnetization and phase change of the switching medium. For illustrative convenience, memory cell 101 and device 100 are referred collectively as “device 100” hereinafter unless the context makes it clear that the term refers solely to device 100.
In the present embodiment, device 100 is amorphous-silicon-based RRAM and uses amorphous silicon as switching medium 104. The resistance of the switching medium 104 changes according to formation or retrieval of a conductive filament inside the a-Si switching medium according to voltage applied. Top electrode 106 is a conductive layer containing silver (Ag) and acts as the source of filament-forming ions in the a-Si structure. Although silver is used in the present embodiment, it will be understood that the top electrode can be formed from various other suitable metals, such as gold (Au), nickel (Ni), aluminum (AI), chromium (Cr), iron (Fe), manganese (Mn), tungsten (W), vanadium (V), and cobalt (Co). Bottom electrode 102 is a boron-doped or other p-type polysilicon electrode 130 that is in contact with a lower end face of the a-Si structure.
In an embodiment, device 100 illustrates a rectifying switching characteristic. Device 100 shows a diode-like behavior at ON-state so that the current in ON-state only flow at positive bias but not at negative bias. Device 100, however, remains in ON-state even though no current is detected as long as the applied negative voltage does not equal or exceed Veth.
Filament 305 is believed to be comprised of a collection of metal particles that are separated from each other by the non-conducting switching medium and does not define a continuous conductive path, unlike the path 303 in the metallic region. Filament 305 extends about 2-10 nm depending on implementation. The conduction mechanism in the ON state is electrons tunneling through the metal particles in the filament. The device resistance is dominated by the tunneling resistance between a metal particle 306 and the bottom electrode. Metal particle 306 is the metal particle in the filament region that is closest to the bottom electrode and is the last metal particle in the filament region in the ON state.
In an embodiment, the resistance ratio between the ON/OFF states ranges from 10E3 to 10E7. Device 100 behaves like a resistor in the ON state and a capacitor in the OFF state (i.e., the switching medium does not conduct current in any meaningful amount and behaves as a dielectric in the OFF state). In an implementation, the resistance is 10E5 Ohm in the ON state and 10E10 Ohm in the OFF state. In another implementation, the resistance is 10E4 Ohm in the ON state and 10E9 Ohm in the OFF state. In yet another implementation, the resistance is at least 10E7 Ohm in the OFF state.
In an embodiment, device 100 exhibits controllable ON-state current flow of 10 nA-10 mA and endurance of greater 10E6. Device 100 exhibits relatively a retention time of 6 years at room temperature.
Resistive memory 402 includes a bottom electrode 404, a switching medium 406, and a top electrode 408. Switching medium 406 exhibits a resistance that can be selectively set to various values according to the voltages applied to the top and bottom electrodes 408, 404. Resistive memory 402 corresponds to memory cell 100 and in this example, is connected with a select transistor 412 in series. Select transistor 412 controls the location of the switching element to be accessed.
Crossbar memory array 500 includes a parallel array of bottom electrodes 502 extending along a first direction. In an embodiment, bottom electrodes 502 includes a bottom metal (not shown) and a polycrystalline silicon-germanium (not shown) formed on the bottom metal. The bottom electrodes are nanoscale in the present embodiment. For example, the bottom electrodes have a width of about 40 nm and pitch of about 60 nm.
A parallel array of top electrodes 504 extends along a second direction to intersect the bottom electrodes. The top electrodes include metal capable of supplying filament forming ions such as silver (Ag), gold (Au), nickel (Ni), aluminum (AI), chromium (Cr), iron (Fe), manganese (Mn), tungsten (W), vanadium (V) and cobalt (Co). In an embodiment, the top electrodes and the bottom electrodes are orthogonal to each other. The top electrodes are nanowires having a width of about 60 nm and a pitch of about 150 nm.
Each intersection 506 of the two arrays defines a two-terminal resistive memory cell 508. Examples of cell 508 include two-terminal device 100 shown in
The crossbar memory array as described above may be fabricated on a silicon substrate, as illustrated in
Bottom electrode 604 includes a bottom metal layer 610 formed on a substrate and a p-type polysilicon layer 612 formed on the bottom metal layer. The p-type polysilicon layer has a thickness of 10˜30 nm, and the bottom metal layer has a thickness of about 150 nm according to an implementation. The thicknesses of these layers may vary depending on implementation. In the present embodiment, p-type polysilicon layer 612 is a boron-doped polysilicon, and bottom metal layer 610 is made of metal, e.g., tungsten, aluminum or copper, or an alloy thereof. In an implementation, the bottom metal is replaced with non-metal material that has a higher conductivity than the p-type polysilicon layer.
P-type polysilicon 612 facilitates the defect site formation in the a-Si switching medium to be controllable by enabling the tuning of the amorphous silicon deposition on the p-type polysilicon, so that the defect density in the filament region does not become too high. When metal, e.g., Nickel or other metal, is used as a platform whereon the amorphous silicon switching layer is formed, the inventors have found that the filament formation was difficult to control due to the excess number of defect sites formed at the a-Si/metal interface. Furthermore, a-Si can react with the bottom metal electrode during the a-Si deposition, giving a-Si and metal alloy (silicide) at the interface. Accordingly, in addition to serving as an electrode, p-type polysilicon 612 serves as a platform that enables defect formation in the aSi switching layer to be controllable, e.g. layer 612 is an interface layer.
One issue associated with the use of polysilicon as part of bottom electrode 604 is the relatively high deposition temperature needed for polysilicon. Typically, polysilicon is deposited by pyrolyzing silane (SiH4) at 580 to 650° C. and the dopants provided therein are activated at 800° C. or higher temperature. However, a CMOS compatible backend process preferably should have thermal budget of 450° C. to limit damage or degradation of the existing structures (underlying CMOS devices, e.g. transistor 412). For example, if exposed to high temperature, aluminum interconnect may be degraded due to its low melting temperature. The relatively high deposition temperature of polysilicon can limit the use of resistive memory 600 in a backend process. Reducing the polysilicon deposition temperature to 450° C. or less, however, may hinder crystal formation and cause the resulting material to have undesirably high resistance. In addition, lowering the temperature decreases the deposition rate of polysilicon significantly and could make the fabrication process impractical.
Resistive memory 650 includes a bottom electrode 654, a switching layer 656, and a top electrode 658. Switching layer 656 is provided between the top and bottom electrodes and includes a-Si material whose resistance can be made to vary according to voltages applied. Resistive memory 650 is formed over a substrate 652. Substrate 652 maybe a semiconductor substrate, e.g., a silicon substrate or a compound substrate of a III-V or II-VI type. In an embodiment, the substrate is not made of semiconductor material, e.g., is made of plastic.
In an embodiment, resistive memory is formed in a backend process. Accordingly, substrate 652 may include transistors, metal interconnects, and other circuits so that resistive memory 650 overlies one or more of these circuit components. Because these are formed before the resistive memory, these are termed herein as front-end CMOS processes.
In an embodiment, bottom electrode 654 includes a bottom metal layer 660 formed on a substrate and a polycrystalline semiconductor layer (e.g., poly-SiGe layer) 662 (e.g. an interface layer) formed on the bottom metal layer. Poly-SiGe layer 662 has a thickness of 10 30 nm, and bottom metal layer 660 has a thickness of about 150 nm according to an implementation. The thicknesses of these layers may vary depending on implementation. Poly-SiGe layer 662 is boron-doped, and bottom metal layer 660 is made of metal, e.g., tungsten, aluminum or copper, or an alloy thereof. In an implementation, the bottom metal is replaced with nonmetal material that has a higher conductivity than the poly-SiGe layer.
Poly-SiGe 662 film exhibits many properties comparable to polysilicon. Like polysilicon, poly-SiGe 662 facilitates the defect site formation in the a-Si switching medium, so that the defect density in the filament region does not become too high. In addition to poly-SiGe, the polycrystalline semiconductor layer may include III-V type semiconductor compounds (such as Gallium Arsenide GaAs, Gallium Nitride GaN, Boron Nitride BN etc.) or II-VI type semiconductor compounds (such as Cadmium Selenide, Zinc Telluride etc.).
Switching layer 656 exhibits a resistance that can be selectively set to various values, and reset, using appropriate control circuitry. In an embodiment, switching layer 656 includes an a-Si structure having a thickness of 20-80 nm. The thickness of the amorphous silicon structure varies depending on the device size and configuration. In an embodiment, the a-Si structure is a film wherein the width and length are substantially greater than the thickness. Alternatively, the a-Si structure may be a pillar wherein the vertical dimension is more pronounced than the dimensions of width and length.
In an embodiment, switching layer 656 includes non-crystalline silicon structures, such as amorphous polysilicon (sometimes called nanocrystalline silicon, an amorphous phase that includes small grains of crystalline silicon). As used herein, the term “noncrystalline silicon” refers to amorphous silicon or amorphous poly-SiGe that exhibits controllable resistance, a combination thereof, or the like.
Top electrode 658 contains silver (Ag) as the source of filament-forming metal ions in the switching medium. In an embodiment, top electrode 658 includes an Ag film with a thickness of 150 nm. In other embodiments, the top electrode includes a stacked structure. For example, a Ag layer of about 50 nm is deposited on top of a-Si and another metal (e.g., TiN/W) of about 100 nm can be deposited on top of the Ag layer. The thickness may vary depending on the device size and implementation. Although silver is used in the present embodiment, it will be understood that the top electrode can be formed from various other suitable metals, such as gold (Au), nickel (Ni), aluminum (AI), chromium (Cr), iron (Fe), manganese (Mn), tungsten (W), vanadium (V), cobalt (Co) or a metal stack (or stacks).
A bottom metal layer 704 is formed over substrate 702 (
An interfacelayer, e.g. polycrystalline semiconductor layer (e.g., poly-SiGe layer) 706 is formed over bottom metal layer 704 to define the bottom electrode having the bottom metal and the polycrystalline semiconductor layer (
Poly-SiGe 706 layer is deposited over the bottom electrode at a relatively low temperature of 450° C. or less, e.g., 380-420° C., so that the formation of resistive memory 650 may be implemented in a CMOS compatible back-end process on IC substrate 702.
In an embodiment, poly-SiGe layer 706 is deposited by using a low pressure chemical vapor deposition (LPCVD) process at a chamber pressure of 2 Torr, at 400° C. The deposition temperature is lowered by increasing the concentration of Ge, so that the resulting poly-SiGe has the Ge concentration of about 70%. Gases input into the process chamber include: diborane (1%, H2 balance) at 10 sccm, SiH4 at 7 sccm, and GeH4 (10%) at 40 sccm. P-type impurities are doped into poly-SiGe by in-situ doping using B2H6 or BCh, or both. In various embodiments, the process for forming the interface layer is also compatible with IC foundry compatible processes.
In addition to LPCVD, other deposition techniques may also be used to deposit poly-SiGe over the bottom electrode, e.g., atmospheric pressure CVD (APCVD), ultra-high vacuum CVD (UHVCVD), aerosol assisted CVD (AACVD), plasma enhanced CVD (PECVD), microwave plasma assisted CVD (MPCVD), atomic layer CVD (ALCVD) or atomic layer epitaxy, hybrid physical-chemical vapor deposition (HPCVD), hot wire CVD (HWCVD), direct liquid injection CVD (DLICVD) and vapor phase epitaxy (VPE).
Referring to
An amorphous silicon layer 712 is formed on the p-type poly-SiGe to a thickness of 2-30 nm (
Referring to
A number of embodiments have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. For example, the ordering of layers on the substrate could be reversed, where the top electrode is provided below the bottom electrode depending on implementation. Accordingly the terms “top” and “bottom” should not be used to limit the relative positions of the source electrode that provides the filament-forming ions in the a-Si structure and an electrode provided at its opposing side. Accordingly, other embodiments are within the scope of the following claims.
The present application is a continuation-in-part of application Ser. No. 13/725,331 filed Dec. 21, 2012, which is a continuation of application Ser. No. 12/833,898 filed Jul. 9, 2010, now U.S. Pat. No. 8,374,018 issued Feb. 12, 2013.
Number | Name | Date | Kind |
---|---|---|---|
4433468 | Kawamata | Feb 1984 | A |
4684972 | Owen et al. | Aug 1987 | A |
4741601 | Saito | May 1988 | A |
5139911 | Yagi et al. | Aug 1992 | A |
5242855 | Oguro | Sep 1993 | A |
5278085 | Maddox, III et al. | Jan 1994 | A |
5315131 | Kishimoto et al. | May 1994 | A |
5335219 | Ovshinsky et al. | Aug 1994 | A |
5360981 | Owen et al. | Nov 1994 | A |
5457649 | Eichman et al. | Oct 1995 | A |
5538564 | Kaschmitter | Jul 1996 | A |
5541869 | Rose et al. | Jul 1996 | A |
5594363 | Freeman et al. | Jan 1997 | A |
5614756 | Forouhi et al. | Mar 1997 | A |
5645628 | Endo et al. | Jul 1997 | A |
5714416 | Eichman et al. | Feb 1998 | A |
5751012 | Wolstenholme et al. | May 1998 | A |
5840608 | Chang | Nov 1998 | A |
5970332 | Pruijmboom et al. | Oct 1999 | A |
5998244 | Wolstenholme et al. | Dec 1999 | A |
6122318 | Yamaguchi et al. | Sep 2000 | A |
6128214 | Kuekes et al. | Oct 2000 | A |
6143642 | Sur, Jr. et al. | Nov 2000 | A |
6180998 | Crafts | Jan 2001 | B1 |
6259116 | Shannon | Jul 2001 | B1 |
6291836 | Kramer et al. | Sep 2001 | B1 |
6436765 | Liou et al. | Aug 2002 | B1 |
6436818 | Hu et al. | Aug 2002 | B1 |
6492694 | Noble et al. | Dec 2002 | B2 |
6627530 | Li et al. | Sep 2003 | B2 |
6762474 | Mills, Jr. | Jul 2004 | B1 |
6768157 | Krieger et al. | Jul 2004 | B2 |
6806526 | Krieger et al. | Oct 2004 | B2 |
6815286 | Krieger et al. | Nov 2004 | B2 |
6838720 | Krieger et al. | Jan 2005 | B2 |
6848012 | LeBlanc et al. | Jan 2005 | B2 |
6858481 | Krieger et al. | Feb 2005 | B2 |
6858482 | Gilton | Feb 2005 | B2 |
6864127 | Yamazaki et al. | Mar 2005 | B2 |
6864522 | Krieger et al. | Mar 2005 | B2 |
6881994 | Lee et al. | Apr 2005 | B2 |
6927430 | Hsu | Aug 2005 | B2 |
6939787 | Ohtake et al. | Sep 2005 | B2 |
6946719 | Petti et al. | Sep 2005 | B2 |
7020006 | Chevallier et al. | Mar 2006 | B2 |
7023093 | Canaperi et al. | Apr 2006 | B2 |
7026702 | Krieger et al. | Apr 2006 | B2 |
7102150 | Harshfield et al. | Sep 2006 | B2 |
7122853 | Gaun et al. | Oct 2006 | B1 |
7187577 | Wang et al. | Mar 2007 | B1 |
7221599 | Gaun et al. | May 2007 | B1 |
7238607 | Dunton et al. | Jul 2007 | B2 |
7254053 | Krieger et al. | Aug 2007 | B2 |
7289353 | Spitzer et al. | Oct 2007 | B2 |
7324363 | Kerns et al. | Jan 2008 | B2 |
7365411 | Campbell | Apr 2008 | B2 |
7405418 | Happ et al. | Jul 2008 | B2 |
7426128 | Scheuerlein | Sep 2008 | B2 |
7433253 | Gogl et al. | Oct 2008 | B2 |
7474000 | Scheuerlein et al. | Jan 2009 | B2 |
7479650 | Gilton | Jan 2009 | B2 |
7499355 | Scheuerlein et al. | Mar 2009 | B2 |
7521705 | Liu | Apr 2009 | B2 |
7534625 | Karpov et al. | May 2009 | B2 |
7541252 | Eun et al. | Jun 2009 | B2 |
7550380 | Elkins et al. | Jun 2009 | B2 |
7566643 | Czubatyi et al. | Jul 2009 | B2 |
7606059 | Toda | Oct 2009 | B2 |
7615439 | Schricker et al. | Nov 2009 | B1 |
7629198 | Kumar et al. | Dec 2009 | B2 |
7719001 | Nomura et al. | May 2010 | B2 |
7728318 | Raghuram et al. | Jun 2010 | B2 |
7729158 | Toda et al. | Jun 2010 | B2 |
7749805 | Pinnow et al. | Jul 2010 | B2 |
7772581 | Lung | Aug 2010 | B2 |
7778063 | Brubaker et al. | Aug 2010 | B2 |
7786464 | Nirschl et al. | Aug 2010 | B2 |
7786589 | Matsunaga et al. | Aug 2010 | B2 |
7824956 | Schricker et al. | Nov 2010 | B2 |
7829875 | Scheuerlein | Nov 2010 | B2 |
7835170 | Bertin et al. | Nov 2010 | B2 |
7859884 | Scheuerlein | Dec 2010 | B2 |
7875871 | Kumar et al. | Jan 2011 | B2 |
7881097 | Hosomi et al. | Feb 2011 | B2 |
7897953 | Liu | Mar 2011 | B2 |
7898838 | Chen et al. | Mar 2011 | B2 |
7920412 | Hosotani et al. | Apr 2011 | B2 |
7924138 | Kinoshita et al. | Apr 2011 | B2 |
7968419 | Li et al. | Jun 2011 | B2 |
7972897 | Kumar et al. | Jul 2011 | B2 |
7984776 | Sastry et al. | Jul 2011 | B2 |
8004882 | Katti et al. | Aug 2011 | B2 |
8018760 | Muraoka et al. | Sep 2011 | B2 |
8021897 | Sills et al. | Sep 2011 | B2 |
8045364 | Schloss et al. | Oct 2011 | B2 |
8054674 | Tamai et al. | Nov 2011 | B2 |
8067815 | Chien et al. | Nov 2011 | B2 |
8071972 | Lu et al. | Dec 2011 | B2 |
8084830 | Kanno et al. | Dec 2011 | B2 |
8088688 | Herner | Jan 2012 | B1 |
8097874 | Venkatasamy et al. | Jan 2012 | B2 |
8102698 | Scheuerlein | Jan 2012 | B2 |
8143092 | Kumar et al. | Mar 2012 | B2 |
8144498 | Kumar et al. | Mar 2012 | B2 |
8164948 | Katti et al. | Apr 2012 | B2 |
8168506 | Herner | May 2012 | B2 |
8183553 | Phatak et al. | May 2012 | B2 |
8187945 | Herner | May 2012 | B2 |
8198144 | Herner | Jun 2012 | B2 |
8207064 | Bandyopadhyay et al. | Jun 2012 | B2 |
8227787 | Kumar et al. | Jul 2012 | B2 |
8231998 | Sastry et al. | Jul 2012 | B2 |
8233308 | Schricker et al. | Jul 2012 | B2 |
8237146 | Kreupl et al. | Aug 2012 | B2 |
8258020 | Herner | Sep 2012 | B2 |
8265136 | Hong et al. | Sep 2012 | B2 |
8274812 | Nazarian et al. | Sep 2012 | B2 |
8315079 | Kuo et al. | Nov 2012 | B2 |
8320160 | Nazarian | Nov 2012 | B2 |
8374018 | Lu | Feb 2013 | B2 |
8385100 | Kau et al. | Feb 2013 | B2 |
8394670 | Herner | Mar 2013 | B2 |
8441835 | Jo et al. | May 2013 | B2 |
8467227 | Jo | Jun 2013 | B1 |
8587989 | Manning et al. | Nov 2013 | B2 |
8658476 | Sun et al. | Feb 2014 | B1 |
8659003 | Herner et al. | Feb 2014 | B2 |
20030141565 | Hirose et al. | Jul 2003 | A1 |
20030174574 | Perner et al. | Sep 2003 | A1 |
20030206659 | Hamanaka | Nov 2003 | A1 |
20040026682 | Jiang | Feb 2004 | A1 |
20040170040 | Rinerson et al. | Sep 2004 | A1 |
20050020510 | Benedict | Jan 2005 | A1 |
20050029587 | Harshfield | Feb 2005 | A1 |
20050041498 | Resta et al. | Feb 2005 | A1 |
20050052915 | Herner et al. | Mar 2005 | A1 |
20050062045 | Bhattacharyya | Mar 2005 | A1 |
20050073881 | Tran et al. | Apr 2005 | A1 |
20050175099 | Sarkijarvi et al. | Aug 2005 | A1 |
20060017488 | Hsu | Jan 2006 | A1 |
20060281244 | Ichige et al. | Dec 2006 | A1 |
20070008773 | Scheuerlein | Jan 2007 | A1 |
20070015348 | Hsu et al. | Jan 2007 | A1 |
20070045615 | Cho et al. | Mar 2007 | A1 |
20070087508 | Herner | Apr 2007 | A1 |
20070090425 | Kumar et al. | Apr 2007 | A1 |
20070091685 | Guterman et al. | Apr 2007 | A1 |
20070105284 | Herner | May 2007 | A1 |
20070105390 | Oh | May 2007 | A1 |
20070205510 | Lavoie et al. | Sep 2007 | A1 |
20070228414 | Kumar et al. | Oct 2007 | A1 |
20070284575 | Li et al. | Dec 2007 | A1 |
20070290186 | Bourim et al. | Dec 2007 | A1 |
20070291527 | Tsushima et al. | Dec 2007 | A1 |
20070295950 | Cho et al. | Dec 2007 | A1 |
20070297501 | Hussain et al. | Dec 2007 | A1 |
20080002481 | Gogl et al. | Jan 2008 | A1 |
20080006907 | Lee et al. | Jan 2008 | A1 |
20080048164 | Odagawa | Feb 2008 | A1 |
20080089110 | Robinett et al. | Apr 2008 | A1 |
20080090337 | Williams | Apr 2008 | A1 |
20080106925 | Paz de Araujo et al. | May 2008 | A1 |
20080106926 | Brubaker et al. | May 2008 | A1 |
20080185567 | Kumar et al. | Aug 2008 | A1 |
20080198934 | Hong et al. | Aug 2008 | A1 |
20080205179 | Markert et al. | Aug 2008 | A1 |
20080206931 | Breuil et al. | Aug 2008 | A1 |
20080220601 | Kumar et al. | Sep 2008 | A1 |
20080232160 | Gopalakrishnan | Sep 2008 | A1 |
20080278990 | Kumar et al. | Nov 2008 | A1 |
20080304312 | Ho et al. | Dec 2008 | A1 |
20080311722 | Petti et al. | Dec 2008 | A1 |
20090001345 | Schricker et al. | Jan 2009 | A1 |
20090003717 | Sekiguchi et al. | Jan 2009 | A1 |
20090014707 | Lu et al. | Jan 2009 | A1 |
20090052226 | Lee et al. | Feb 2009 | A1 |
20090095951 | Kostylev et al. | Apr 2009 | A1 |
20090152737 | Harshfield | Jun 2009 | A1 |
20090168486 | Kumar | Jul 2009 | A1 |
20090231910 | Liu et al. | Sep 2009 | A1 |
20090250787 | Kutsunai | Oct 2009 | A1 |
20090256130 | Schricker | Oct 2009 | A1 |
20090257265 | Chen et al. | Oct 2009 | A1 |
20090267047 | Sasago et al. | Oct 2009 | A1 |
20090298224 | Lowrey | Dec 2009 | A1 |
20090321789 | Wang et al. | Dec 2009 | A1 |
20100007937 | Widjaja et al. | Jan 2010 | A1 |
20100012914 | Xu et al. | Jan 2010 | A1 |
20100019221 | Lung et al. | Jan 2010 | A1 |
20100019310 | Sakamoto | Jan 2010 | A1 |
20100032638 | Xu | Feb 2010 | A1 |
20100032640 | Xu | Feb 2010 | A1 |
20100034518 | Iwamoto et al. | Feb 2010 | A1 |
20100044708 | Lin et al. | Feb 2010 | A1 |
20100046622 | Doser et al. | Feb 2010 | A1 |
20100084625 | Wicker et al. | Apr 2010 | A1 |
20100085798 | Lu et al. | Apr 2010 | A1 |
20100090192 | Goux et al. | Apr 2010 | A1 |
20100101290 | Bertolotto | Apr 2010 | A1 |
20100102290 | Lu et al. | Apr 2010 | A1 |
20100157651 | Kumar et al. | Jun 2010 | A1 |
20100157710 | Lambertson et al. | Jun 2010 | A1 |
20100163828 | Tu | Jul 2010 | A1 |
20100176368 | Ko et al. | Jul 2010 | A1 |
20100219510 | Scheuerlein et al. | Sep 2010 | A1 |
20100221868 | Sandoval | Sep 2010 | A1 |
20100321095 | Mikawa et al. | Dec 2010 | A1 |
20110006275 | Roelofs et al. | Jan 2011 | A1 |
20110089391 | Mihnea et al. | Apr 2011 | A1 |
20110128779 | Redaelli et al. | Jun 2011 | A1 |
20110133149 | Sonehara | Jun 2011 | A1 |
20110136327 | Han et al. | Jun 2011 | A1 |
20110155991 | Chen | Jun 2011 | A1 |
20110194329 | Ohba et al. | Aug 2011 | A1 |
20110198557 | Rajendran et al. | Aug 2011 | A1 |
20110204312 | Phatak | Aug 2011 | A1 |
20110205782 | Costa et al. | Aug 2011 | A1 |
20110212616 | Seidel et al. | Sep 2011 | A1 |
20110227028 | Sekar et al. | Sep 2011 | A1 |
20110284814 | Zhang | Nov 2011 | A1 |
20110299324 | Li et al. | Dec 2011 | A1 |
20110305064 | Jo et al. | Dec 2011 | A1 |
20110312151 | Herner | Dec 2011 | A1 |
20110317470 | Lu et al. | Dec 2011 | A1 |
20120001146 | Lu et al. | Jan 2012 | A1 |
20120007035 | Jo et al. | Jan 2012 | A1 |
20120008366 | Lu | Jan 2012 | A1 |
20120012806 | Herner | Jan 2012 | A1 |
20120015506 | Jo et al. | Jan 2012 | A1 |
20120025161 | Rathor et al. | Feb 2012 | A1 |
20120033479 | Delucca et al. | Feb 2012 | A1 |
20120043519 | Jo et al. | Feb 2012 | A1 |
20120043520 | Herner et al. | Feb 2012 | A1 |
20120043621 | Herner | Feb 2012 | A1 |
20120043654 | Lu et al. | Feb 2012 | A1 |
20120076203 | Sugimoto et al. | Mar 2012 | A1 |
20120080798 | Harshfield | Apr 2012 | A1 |
20120104351 | Wei et al. | May 2012 | A1 |
20120108030 | Herner | May 2012 | A1 |
20120140816 | Franche et al. | Jun 2012 | A1 |
20120142163 | Herner | Jun 2012 | A1 |
20120145984 | Rabkin et al. | Jun 2012 | A1 |
20120155146 | Ueda et al. | Jun 2012 | A1 |
20120205606 | Lee et al. | Aug 2012 | A1 |
20120220100 | Herner | Aug 2012 | A1 |
20120235112 | Huo et al. | Sep 2012 | A1 |
20120236625 | Ohba et al. | Sep 2012 | A1 |
20120269275 | Hannuksela | Oct 2012 | A1 |
20120305874 | Herner | Dec 2012 | A1 |
20120326265 | Lai et al. | Dec 2012 | A1 |
20130020548 | Clark et al. | Jan 2013 | A1 |
Number | Date | Country |
---|---|---|
2408035 | Jan 2012 | EP |
2405441 | Nov 2012 | EP |
2005-506703 | Mar 2005 | JP |
2006-032951 | Feb 2006 | JP |
2007-067408 | Mar 2007 | JP |
2007-281208 | Oct 2007 | JP |
2007-328857 | Dec 2007 | JP |
10-2011-0014248 | Feb 2011 | KR |
WO 03034498 | Apr 2003 | WO |
WO 2009005699 | Jan 2009 | WO |
Entry |
---|
Office Action for U.S. Appl. No. 13/434,567, dated Feb. 6, 2014. |
Office Action for U.S. Appl. No. 13/620,012, dated Feb. 11, 2014. |
Notice of Allowance for U.S. Appl. No. 13/468,201, dated Feb. 20, 2014. |
Office Action for U.S. Appl. No. 12/625,817, dated Feb. 28, 2014. |
Office Action for U.S. Appl. No. 12/835,704, dated Mar. 14, 2014. |
Office Action for U.S. Appl. No. 13/870,919, Dated Apr. 3, 2014. |
Office Action for U.S. Appl. No. 13/167,920, dated Mar. 12, 2014. |
International Search Report and Written Opinion for PCT/US2013/077628, filed on Dec. 23, 2013. |
Jian Hu et al., “Area-Dependent Switching in Thin Film-Silicon Devices”, Materials Research Society Proceedings, 2003, pp. AI8.3.1-AI8.3.6, vol. 762, No. 1, Cambridge University Press. |
Andre Dehon, “Array-Based Architecture for FET-Based, Nanoscale Electronics”, IEEE Transactions on Nanotechnology, Mar. 2003, pp. 23-32, vol. 2, No. 1. |
Herb Goronkin et al., “High-Performance Emerging Solid-State Memory Technologies”, MRS Bulletin, Nov. 2004, pp. 805-813, www.mrs.org/publications/bulletin. |
Gerhard Muller et al., “Status and Outlook of Emerging Nonvolatile Memory Technologies”, IEEE, 2004, pp. 567-570. |
A.E. Owen et al., “Memory Switching in Amorphous Silicon Devices”, Journal of Non-Crystalline Solids 59 & 60, 1983, pp. 1273-1280, North-Holland Publishing Company. |
J. Campbell Scott, “Is There an Immortal Memory?”, www.sciencemag.org, Apr. 2, 2004, pp. 62-63, vol. 304, No. 5667. |
S.H. Lee et al., “Full Integration and Cell Characteristics for 64Mb Nonvolatile PRAM”, 2004 Symposium on VLSI Technology Digest of Technical Papers, pp. 20-21, 2004 IEEE. |
Stephen Y. Chou et al., “Imprint Lithography With 25-Nanometer Resolution”, Science, Apr. 5, 1996, pp. 85-87, vol. 272. |
S. Zankovych et al., “Nanoimprint Lithography: Challenges and Prospects”, Institute of Physics Publishing, Nanotechnology 12, 2001, pp. 91-95. |
A. Avila et al., “Switching in Coplanar Amorphous Hydrogenated Silicon Devices”, Solid-State Electronics 44, 2000, pp. 17-27. |
Jian Hu et al., “Switching and Filament Formation in Hot-Wire CVD P-Type A-Si:H Devices”, Science Direct, Thin Solid Films 430, 2003, pp. 249-252, www.sciencedirect.com. |
S. Hudgens et al,. “Overview of Phase-Change Chalcogenide Nonvolatile Memory Technology”, MRS Bulletin, Nov. 2004, pp. 829-832, www.mrs.org/publications/bulletin. |
K. Terabe et al., “Quantized Conductance Atomic Switch”, Nature, vol. 433, Jan. 6, 2005, pp. 47-50, www.nature.com/ nature. |
Michael Kund et al., “Conductive Bridging RAM (CBRAM): An Emerging Non-Volatile Memory Technology Scalable to Sub 20nm”, IEEE, 2005. |
W. Den Boer, “Threshold Switching in Hydrogenated Amorphous Silicon”, American Institute of Physics, 1982, pp. 812-813. |
P.G. Lecomber et al., “The Switching Mechnism in Amorphous Silicon Junctions”, Journal of Non-Crystalline Solids 77 & 78, 1985, pp. 1373-1382, North-Holland, Amsterdam. |
A. E. Owen et al., “Switching in Amorphous Devices”, Int. J. Electronics, 1992, pp. 897-906, vol. 73, No. 5. |
M. Jafar et al., “Switching in Amorphous-Silicon Devices”, The American Physical Society, 1994, pp. 611-615, vol. 49, No. 19. |
Stikeman, Alexandra, “Polymer Memory—The Plastic Path to Beller Data Storage,” Technology Review, Sep. 2002, p. 31, www.technology review.com. |
Yong Chen et al. “Nanoscale molecular-switch crossbar circuits,” Nanotechnology 14, 2003, pp. 462-468, vol. 1.14, Institute of Physics Publishing. |
C.P. Collier et al. “Electronically Configurable Molecular-Based Logic Gates,” Science, Jul. 16, 1999, pp. 391-395, vol. 285, No. 5426. |
Office Action for U.S. Appl. No. 11/875,541, dated Jul. 22, 2010. |
Office Action for U.S. Appl. No. 11/875,541, dated Mar. 30, 2011. |
Office Action for U.S. Appl. No. 11/875,541, dated Oct. 5, 2011. |
Office Action for U.S. Appl. No. 11/875,541, dated Jun. 8, 2012. |
Sung-Hyun Jo et al., “A Silicon-Based Crossbar Ultra-High-Density Non-Volatile Memory”, SSEL Annual Report 2007. |
International Search Report for PCT/US2009/060023, filed on Oct. 8, 2009. |
Waser, R et al., “Nanoionics-based Resistive Switching Memories”, Nature Materials, Nov. 2007, pp. 833-835, vol. 6. |
Written Opinion of the International Searching Authority for PCT/US2009/060023, filed on Oct. 8, 2009. |
Ex Parte Quayle Action for U.S. Appl. No. 12/826,653, dated May 8, 2012. |
International Search Report for PCT/US2011/040090, filed on Jun. 10, 2011. |
Written Opinion of the International Searching Authority for PCT/US2011/040090, filed on Jun. 10, 2011. |
Notice of Allowability for U.S. Appl. No. 13/158,231, dated Apr. 17, 2012. |
Office Action for U.S. Appl. No. 12/835,704, dated Sep. 21, 2011. |
Office Action for U.S. Appl. No. 12/835,704, dated Mar. 1, 2012. |
Advisory Action for U.S. Appl. No. 12/835,704, dated Jun. 8, 2012. |
International Search Report and Written Opinion for PCT/US2011/046035, filed on Jul. 29, 2011. |
Office Action for U.S. Appl. No. 12/861,650, dated Jan. 25, 2012. |
Notice of Allowability for U.S. Appl. No. 12/861,650, dated Jun. 19, 2012. |
Sung Hyun Jo et al., “Programmable Resistance Switching in Nanoscale Two-Terminal Devices,” Supporting Information, Dec. 29, 2008, pp. 1-4, vol. 9. No. 1, Department of Electrical Engineering and Computer Science, The University of Michigan, Ann Arbor, Michigan. |
Kuk-Hwan Kim et al., “Nanoscale resistive memory with intrinsic diode characteristics and long endurance,” Applied Physics Letters, 2010, pp. 053106-1-053106-3, vol. 96, American Institute of Physics. |
Sung Hyun Jo et al., Si-Based Two-Terminal Resistive Switching Nonvolatile Memory, 2008, IEEE. |
Sung Hyun Jo et al., “Nanoscale Memristor Device as Synapse in Neuromorphic Systems”, Nano Letters, 2010, pp. 1297-1301, pubs.acs.org/NanoLett, A-E, American Chemical Society Publications. |
Wei Lu et al., “Nanoelectronics from the bottom up,” Nature Materials—Review Articles | Insight, www.nature.com/naturematerials, Nov. 2007, pp. 841-850, vol. 6, Nature Publishing Group. |
Sung Hyun Jo et al., “Ag/a-Si:H/c-Si Resistive Switching Nonvolatile Memory Devices,” 2006. |
Sung Hyun Jo et al., “Experimental, Modeling and Simulation Studies of Nanoscale Resistance Switching Devices,” 2009, IEEE. |
Sung Hyun Jo et al., “Nonvolatile Resistive Switching Devices Based on Nanoscale Metal/Amorphous Silicon/Crystalline Silicon Junctions,” Mater. Res. Soc. Symp. Proc., 2007, vol. 997, Materials Research Society. |
Sung Hyun Jo et al., “Si Memristive Devices Applied to Memory and Neuromorphic Circuits.” |
Wei Lu et al., “Supporting Information,” 2008. |
Sung Hyun Jo et al., “High-Density Crossbar Arrays Based on a Si Memristive System,” Nano Letters, 2009, pp. 870-874, vol. 9, No. 2, American Chemical Society Publications. |
Sung Hyun Jo et al., “High-Density Crossbar Arrays Based on a Si Memristive System,” Supporting Information, 2009, pp. 1-4. |
Sung Hyun Jo et al., “Programmable Resistance Switching in Nanoscale TwoTerminal Devices,” Nano Letters, 2009, pp. 496-500, vol. 9, No. 1, American Chemical Society Publications. |
Shubhra Gangopadhyay et al., “Memory Switching in Sputtered Hydrogenated Amorphous Silicon (a-Si:H)”, Japanese Journal of Applied Physics, Short Notes, 1985, pp. 1363-1364, vol. 24, No. 10, JPN. J. Appl. Phys. |
S. K. Dey, “Electrothermal model of switching in amorphous silicon films”, J. Vac. Sci. Technol., Jan./Feb.1980, pp. 445-448, vol. 17, No. 1, American Vacuum Society. |
J. Hajto et al., “The Programmability of Amorphous Silicon Analogue Memory Elements”, Mat. Res. Soc. Symp. Proc., 1990, pp. 405-410, vol. 192, Materials Research Society. |
M. J. Rose et al., “Amorphous Silicon Analogue Memory Devices”, Journal of Non-Crystalline Solids 115, 1989, pp. 168-170, Elsevier Science Publishers B.V., North-Holland. |
A. Moopenn et al., “Programmable Synaptic Devices for Electronic Neural Nets”, Control and Computers, 1990, pp. 37-40, vol. 18, No. 2. |
P.G. Le Comber, “Present and Future Applications of Amorphous Silicon and Its Alloys”, Journal of Non-Crystalline Solids 115, 1989, pp. 1-13, Elsevier Science Publishers B.V., North-Holland. |
Hu, J., et. al. “AC Characteristics of Cr/p/sup +/ A-Si:HIV Analog Switching Devices.” IEEE Transactions on Electron Devices, Sep. 2000, pp. 1751-1757, vol. 47, No. 9. |
Owen, A.E. et al., “New amorphous-silicon electrically programmable nonvolatile switching device,” Solid-State and Electron Devices, IEEE Proceedings I, Apr. 1982, pp. 51-54, vol. 129, No. 2. |
J. Hajto et al., “Amorphous & Microcrystalline Semiconductor Devices: vol. 2, Materials and Device Physics”, Mar. 1, 2004, pp. 640-700, Artech House Publishers. |
J. Hajto et al., “Analogue memory and ballistic electron effects in metal-amorphous silicon structures,” Philosophical Magazine B, 1991, pp. 349-369, vol. 63, No. 1, Taylor & Francis Ltd. |
A. J. Holmes et al., “Design of Analogue Synapse Circuits using Non-Volatile a-Si:H Memory Devices”, Proceedings of ISCAS, 1994, pp. 351-354. |
Dong, Y., et al., “Si/a-Si Core/Shell Nanowires as Nonvolatile Crossbar Switches”, Nano Letters, Jan. 2008, pp. 386-391, vol. 8, No. 2. |
European Search Report for Application No. EP 09 81 9890.6 of Mar. 27, 2012. |
D. A. Muller, et al., “The Electronic Structure at the Atomic Scale of Ultrathin Gate Oxides”, Nature, Jun. 1998, pp. 758-761, vol. 399, No. 24. |
Sune, J. et al., “Nondestructive Multiple Breakdown Events in Very Thin SiO2 Films.” Applied Physics Letters, 1989, vol. 55 No. 128. |
Herve Marand, “Materials Engineering Science”, MESc 5025, Chapter 7, University of Vermont, http://www.files.chem.vt.edu/chemdeptimarand/MEScchap6-1 c.pdf. |
Owen, A.E. et al., “Electronic switching in amorphouse silicon devices: properties of the conducting filament”, Proceedings of the 5th International Conference on Solid-State and Integrated Circuit Technology, 1998, pp. 830-833. |
Jo, Sung Hyun, “Nanoscale Memristive Devices for Memory and Logic Applications”, Thesis, University of Michigan, 2010. |
Office Action for U.S. Appl. 12/894,098, dated Aug. 1, 2012. |
Sung Hyun Jo et al., “CMOS Compatible Nanoscale Nonvolatile Resistance Switching Memory,” Nano Letters, 2008, pp. 392-397, vol. 8, No. 2, American Chemical Society Publications. |
Office Action for U.S. Appl. No. 12/582,086, dated Apr. 19, 2011. |
Office Action for U.S. Appl. No. 12/582,086, dated Sep. 6, 2011. |
Notice of Allowance for U.S. Appl. No. 12/582,086, dated Oct. 21, 2011. |
International Search Report for PCT/US2009/061249, filed on Oct. 20, 2009. |
Written Opinion of the International Searching Authority for PCT/US2009/061249, filed on Oct. 20, 2009. |
Office Action for U.S. Appl. No. 12/861,650, dated Oct. 16, 2012. |
Notice of Allowance for U.S. Appl. No. 12/894,087, dated Oct. 25, 2012. |
Notice of Allowance for U.S. Appl. No. 13/149,807, dated Oct. 29, 2012. |
Notice of Allowance for U.S. Appl. No. 12/861,666, dated Nov. 14, 2012. |
Office Action for U.S. Appl. No. 13/156,232, dated Nov. 26, 2012. |
Notice of Allowance for U.S. Appl. No. 13/290,024, dated Nov. 28, 2012. |
Notice of Allowance for U.S. Appl. No. 12/814,410, dated Jan. 8, 2013. |
Corrected Notice of Allowance for U.S. Appl. No. 12/861,666, dated Jan. 11, 2013. |
Supplemental Notice of Allowance for U.S. Appl. No. 12/894,087, dated Jan. 11, 2013. |
Notice of Allowance for U.S. Appl. No. 13/314,513, dated Jan. 24, 2013. |
Notice of Allowance for U.S. Appl. No. 13/118,258, dated Feb. 6, 2013. |
International Search Report and Written Opinion for PCT/US2012/040242, filed May 31, 2012. |
Office Action for U.S. Appl. No. 13/174,264, dated Mar. 6, 2013. |
Office Action for U.S. Appl. No. 13/679,976, dated Mar. 6, 2013. |
Notice of Allowance for U.S. Appl. No. 12/894,098, dated Mar. 15, 2013. |
Office Action for U.S. Appl. No. 13/465,188, dated Mar. 19, 2013. |
Office Action for U.S. Appl. No. 12/861,432, dated Mar. 29, 2013. |
Notice of Allowance for U.S. Appl. No. 13/748,490, dated Apr. 9, 2013. |
Office Action for U.S. Appl. No. 13/725,331, dated May 20, 2013. |
International Search Report and Written Opinion for PCT/US2012/045312, filed on Jul. 2, 2012. |
Office Action for U.S. Appl. No. 13/466,008, dated Jul. 29, 2013. |
Russo, Ugo et al., “Self-Accelerated Thermal Dissolution Model for Reset Programming in Unipolar Resistive-Switching Memory (RRAM) Devices”, IEEE Transactions on Electron Devices, Feb. 2009, pp. 193-200, vol. 56, No. 2. |
Cagli, C. et al., “Evidence for threshold switching in the set process of NiO-based RRAM and physical modeling for set, reset, retention and disturb prediction”, IEEE International Electron Devices Meeting, Dec. 15-17, 2008, pp. 1-4, San Francisco, CA. |
Office Action for U.S. Appl. No. 13/077,941, dated Aug. 12, 2013. |
Office Action for U.S. Appl. No. 13/436,714, dated Aug. 27, 2013. |
Notice of Allowance for U.S. Appl. No. 13/679,976, dated Sep. 17, 2013. |
Office Action for U.S. Appl. No. 13/189,401, dated Sep. 30, 2013. |
Office Action for U.S. Appl. No. 13/462,653, dated Sep. 30, 2013. |
Corrected Notice of Allowance for U.S. Appl. No. 13/733,828, dated Oct. 1, 2013. |
Notice of Allowance for U.S. Appl. No. 13/733,828, dated Aug. 8, 2013. |
Office Action for U.S. Appl. No. 13/594,665, dated Aug. 2, 2013. |
Notice of Allowance for U.S. Appl. No. 13/769,152, dated Oct. 8, 2013. |
Notice of Allowance for U.S. Appl. No. 13/905,074, dated Oct. 8, 2013. |
Notice of Allowance for U.S. Appl. No. 13/452,657, dated Oct. 10, 2013. |
Notice of Allowance for U.S. Appl. No. 13/174,264, dated Oct. 16, 2013. |
Notice of Allowance for U.S. Appl. No. 13/417,135, dated Oct. 23, 2013. |
Notice of Allowance for U.S. Appl. No. 13/725,331, dated Jan. 17, 2014. |
Office Action for U.S. Appl. No. 13/739,283, dated Jan. 16, 2014. |
Office Action for U.S. Appl. No. 13/920,021, dated Jan. 10, 2014. |
Office Action for U.S. Appl. No. 12/861,432, dated Jan. 8, 2014. |
Office Action for U.S. Appl. No. 13/586,815, dated Jan. 29, 2014. |
International Search Report and Written Opinion for PCT/US2013/061244, filed on Sep. 23, 2013. |
Office Action for U.S. Appl. No. 12/835,699, dated Aug. 24, 2011. |
Notice of Allowance for U.S. Appl. No. 12/835,699, dated Feb. 6, 2012. |
Office Action for U.S. Appl. No. 12/833,898, dated Apr. 5, 2012. |
European Search Report for Application No. EP 1100 5207.3 of Oct. 12, 2011. |
Notice of Allowance for U.S. Appl. No. 12/833,898, dated May 30, 2012. |
Notice of Allowance for U.S. Appl. No. 12/939,824, dated May 11, 2012. |
Notice of Allowance for U.S. Appl. No. 12/940,920, dated Oct. 5, 2011. |
Office Action for U.S. Appl. No. 13/314,513, dated Mar. 27, 2012. |
Shong Yin, “Solution Processed Silver Sulfide Thin Films for Filament Memory Applications”, Technical Report No. UCB/EECS-2010-166, http://www.eecs.berkeley.edu/Pubs/TechRpts/2010/EECS-2010-166.html, Dec. 17, 2010, Electrical Engineering and Computer Sciences, University of California at Berkeley. |
Office Action for U.S. Appl. No. 13/149,653, dated Apr. 25, 2012. |
International Search Report for PCT/US2011/045124, filed on Jul. 22, 2011. |
Written Opinion of the international Searching Authority for PCT/US2011/045124, filed on Jul. 22, 2011. |
Peng-Heng Chang et al., “Aluminum spiking at contact windows in Al/Ti—W/Si”, Appl. Phys. Let., Jan. 25, 1988, pp. 272-274, vol. 52 No. 4, American Institute of Physics. |
J. Del Alamo et al., “Operating limits of Al-alloyed high-low junction for BSF solar cells”, Solid-State Electronics, 1981, pp. 415-420, vol. 24, Pergamon Press Ltd., Great Britain. |
Hao-Chih Yuan et al., “Silicon Solar Cells with Front Hetero-Contact and Aluminum Alloy Back Junction”, NREL Conference Paper CP-520-42566, 33rd IEEE Photovoltaic Specialists Conference, May 11-16, 2008, National Renewable Energy Laboratory, San Diego, California. |
Notice of Allowance for U.S. Appl. No. 12/939,824 dated Jul. 24, 2012. |
Office Action for Application No. EP 1100 5207.3 mailed Aug. 8, 2012. |
Office Action for U.S. Appl. No. 13/417,135, dated Oct. 9, 2012. |
Notice of Allowance for U.S. Appl. No. 13/532,019, dated Nov. 14, 2012. |
Office Action for U.S. Appl. No. 13/149,653, dated Nov. 20, 2012. |
Office Action of U.S. Appl. No. 13/436,714, dated Dec. 7, 2012. |
Choi, Jang Wook, Bistable [2]Rotaxane Based Molecular Electronics: Fundamentals and Applications, Dissertation, May 17, 2007, pp. 79-124, California Institute of Technology, Pasadena, California. |
Office Action for U.S. Appl. No. 13/143,047, dated Apr. 11, 2014. |
Office Action for U.S. Appl. No. 13/761,132, dated Apr. 25, 2014. |
Office Action for U.S. Appl. No. 14/072,657, dated Jun. 17, 2014. |
Number | Date | Country | |
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20140054539 A1 | Feb 2014 | US |
Number | Date | Country | |
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Parent | 13725331 | Dec 2012 | US |
Child | 14072657 | US | |
Parent | 12833898 | Jul 2010 | US |
Child | 13725331 | US |