Scalable RRAM device architecture for a non-volatile memory device and method

Information

  • Patent Grant
  • 9412790
  • Patent Number
    9,412,790
  • Date Filed
    Tuesday, December 4, 2012
    12 years ago
  • Date Issued
    Tuesday, August 9, 2016
    8 years ago
Abstract
A method for forming a resistive switching device. The method includes providing a substrate having a surface region and forming a first dielectric material overlying the surface region. A first wiring structure is formed overlying the first dielectric material. The method forms one or more first structure comprising a junction material overlying the first wiring structure. A second structure comprising a stack of material is formed overlying the first structure. The second structure includes a resistive switching material, an active conductive material overlying the resistive switching material, and a second wiring material overlying the active conductive material. The second structure is configured such that the resistive switching material is free from a coincident vertical sidewall region with the junction material.
Description
BACKGROUND

The inventor of the present invention has recognized the success of semiconductor devices has been mainly driven by an intensive transistor down-scaling process. However, as field effect transistors (FETs) approach sizes less than 100 nm, physical problems such as short channel effect begin to hinder proper device operation. For transistor based memories, such as those commonly known as Flash memories, other performance degradations or problems may occur as device sizes shrink. With Flash memories, a high voltage is usually required for programming of such memories, however, as device sizes shrink, the high programming voltage can result in dielectric breakdown and other problems. Similar problems can occur with other types of non-volatile memory devices other than Flash memories.


The inventor of the present invention recognizes that many other types of non-volatile random access memory (RAM) devices have been explored as next generation memory devices, such as: ferroelectric RAM (Fe RAM); magneto-resistive RAM (MRAM); organic RAM (ORAM); phase change RAM (PCRAM); and others.


A common drawback with these memory devices include that they often require new materials that are incompatible with typical CMOS manufacturing. As an example of this, Organic RAM or ORAM requires organic chemicals that are currently incompatible with large volume silicon-based fabrication techniques and foundries. As another example of this, Fe-RAM and MRAM devices typically require materials using a high temperature anneal step, and thus such devices cannot be normally be incorporated with large volume silicon-based fabrication techniques.


Additional drawbacks with these devices include that such memory cells often lack one or more key attributes required of non-volatile memories. As an example of this, Fe-RAM and MRAM devices typically have fast switching (e.g. “0” to “1”) characteristics and good programming endurance, however, such memory cells are difficult to scale to small sizes. In another example of this, for ORAM devices reliability of such memories is often poor. As yet another example of this, switching of PCRAM devices typically includes Joules heating and undesirably require high power consumption.


From the above, improved semiconductor memory devices that can scale to smaller dimensions with reduced drawbacks are therefore desirable.


BRIEF SUMMARY OF THE PRESENT INVENTION

The present invention is directed to resistive switching device. More particularly, embodiments according to the present invention provide a device structure and a method to form a resistive switching device. The resistive switching device has been applied in non-volatile memory device. But it should be recognized that embodiment according to the present invention can have a much broader range of applicability.


In a specific embodiment, a method of forming a resistive switching device for a non-volatile memory device is provided. The method includes providing a substrate having a surface region and forming a first dielectric material overlying the surface region of the substrate. A first wiring structure is formed overlying the first dielectric material and a first junction material comprising a p+ polycrystalline silicon material is deposited overlying at least the first wiring structure. In a specific embodiment, the method forms a hardmask overlying the first junction material. The first junction material is subjected to a first patterning and etching process to form one or more first structure overlying a surface region of the first wiring structure using the hardmask as a masking layer. A second dielectric material is formed overlying the one or more first structures and filling a gap region between the one or more first structures. The method includes depositing a resistive switching material overlying the one or more first structures and a second surface region of the second dielectric material. In a specific embodiment, an active conductive material is formed overlying the resistive switching material. A second wiring material is formed overlying the active conductive material. The method subject a stack of material comprising the second wiring material, the active conductive material, and the resistive switching material to a second patterning process to form a second structure comprising the second wiring material, the active conductive material, and the resistive switching material in a specific embodiment. The first structure including the junction material and the second structure including at least the resistive switching material are configured such that the resistive switching material and the junction material do not share a common sidewall region to inhibit electrical connection between the first wiring structure and the second wiring structure.


In a specific embodiment, a device structure is provided. The device includes a substrate having a service region and a first dielectric material overlying the surface region. A first wiring structure overlies the first dielectric material. In a specific embodiment, the device structure includes a first structure comprising a junction material overlying the first wiring structure. The junction material is configured to be in physical and electrical contact with the first wiring structure. The first structure further includes a first vertical sidewall region. The device structure includes a second structure overlying at least the first structure. In a specific embodiment, the second structure includes a stack of material comprising a resistive switching material in physical and electrical contact with the junction material, an active metal material in physical and electrical contact with the resistive switching material, and a second wiring material in physical and electrical contact with the active metal material. The resistive switching material in the second structure includes a second vertical sidewall region free from a coincident region from the first vertical sidewall region in a specific embodiment.


Many benefits can be achieved by ways of present invention over conventional techniques. For example, the present method provides one or more device structures for forming a resistive switching device. These device structures are free from undesirable electrical connection between terminals for improved yield and enhanced device performance. The present device is characterized by low power consumption (operating voltage no greater than about 6 volts), high switching speed (in nanosecond range), and a high on-state current (Ion) to off-state current (Ioff) ratio (Ion to Ioff ratio greater than about 103). These device properties are desirable for current and future demand for high density, high speed application in consumer electronics, and others. More than one device structures can be realized by ways of present invention for process flexibilities and device design flexibilities. Additionally, the present method uses conventional semiconductor processing techniques without modification to the equipments. Depending on the embodiment, one or more of these benefits may be realized.





SUMMARY OF THE DRAWINGS

In order to more fully understand the present invention, reference is made to the accompanying drawings. Understanding that these drawings are not to be considered limitations in the scope of the invention, the presently described embodiments and the presently understood best mode of the invention are described with additional detail through use of the accompanying drawings in which:



FIG. 1 is a simplified diagram illustrating a fabrication step according to various embodiments of the present invention;



FIG. 1 is a simplified diagram illustrating a resistive switching device for a non-volatile memory device according to an embodiment of the present invention;



FIGS. 2-16 are simplified diagrams illustrating a method for forming a resistive switching device for a non-volatile memory device according to various embodiments of the present invention;



FIGS. 17-19 are simplified diagrams illustrating various partial device structures according to various embodiments of the present invention; and



FIG. 20 is a simplified diagram illustrating an example of an undesirable device structure.





DETAILED DESCRIPTION OF THE PRESENT INVENTION

The present invention is generally related to resistive switching devices. More particularly, embodiments according to the present invention provide a device structure and a method to improve device performance of a resistive switching device The present invention can be applied to improving data retention characteristic of non-volatile memory devices, but it should be recognized that embodiments according to the present invention can have a much broader range of applicability


Some embodiments of a resistive switching device include a two terminal device including a top electrode, a bottom electrode and a resistive switching material disposed between the top electrode and the bottom electrode. The resistive switching material is characterized by a resistance dependent on an electric field upon an application of a suitable voltage to one of the electrodes. The electric field causes a conductor path to form in the resistive switching material. Depending on the electrode material and the resistive switching material used, the conductor path can be formed from the electrode material or defect path in the presence of the electric field. The conductor path determines the resistance of the resistive switching material. For example, for a metal oxide material as the switching material, the conductor path can form from oxygen deficient sites in the metal oxide. For a silicon material as the switching material, the conductor path can be formed from the electrode material, which comprises an active metal material. The resistive switching material is in a high conductance state. The conductor path is broken or retracts when a reverse bias voltage is applied and causes the resistive switching material to be in a low conductance state. The resistance of the resistive switching material has a resistance depending on the voltage and provide for a multi-level or multi-bit device. Therefore the conductor path structure needs to be stable under selected voltage, forward bias voltage, or reverse bias voltage for proper data retention.


Embodiments according to the present invention provide a device structure and a method for a resistive switching device characterized by a stable conductive path when a pre-determined voltage is applied and a reliable data retention characteristic for the device.



FIG. 1 is a simplified diagram illustrating a resistive switching device 100 according to an embodiment of the present invention. The resistive switching device includes a first electrode 102, a second electrode 106, and a resistive switching material 104 sandwiched between the first electrode and the second electrode.


In various embodiments, resistive switching device 100 is formed upon a semiconductor substrate (not shown). In certain embodiments, the semiconductor substrate can have one or more MOS devices formed thereon. The one or more MOS devices can be controlling circuitry for the resistive memory devices in specific embodiments. In other embodiments, the one or more MOS devices may include other functionality, such as a processor, logic, or the like.


In various embodiments, a processor, or the like, may include resistive memory memories as described herein. Because the resistive state-change memories are relatively non-volatile, the states of devices, such as processors, or the like may be maintained while power is not supplied to the processors. To a user, such capability would greatly enhance the power-on power-off performance of devices including such processors. Additionally, such capability would greatly reduce the power consumption of devices including such processors. In particular, because such resistive memories are non-volatile, the processor need not draw power to refresh the memory states, as is common with CMOS type memories. Accordingly, embodiments of the present invention are directed towards processors or other logic incorporating these memory devices, as described herein, devices (e.g. smart phones, network devices) incorporating such memory devices, and the like.


In various embodiments, in FIG. 1, the first electrode 102 can be a first conductor material. The first electrode 102 can include a first conductive material such as a first metal material and/or a doped semiconductor material 112. In a specific embodiment, the first metal material 102 can be tungsten, aluminum, copper or other suitable metal that are compatible with CMOS fabrication techniques. In additional embodiments, a doped semiconductor material 112 may be p-doped polysilicon, p-doped silicon germanium, or the like. In some embodiments, doped semiconductor material 112 may include a lightly doped silicon containing lower layer that acts as a resistive layer, and a highly doped silicon containing upper layer that acts as a conductive layer. In one example, a p+ doped silicon germanium layer having a thickness of about 10-50 nm, e.g. 40 nm is on top of a p− doped silicon germanium layer having a thickness of about 50-100 nm, e.g. 50 nm. In a specific embodiment, the first electrode is elongated in shape and configured to extend in a first direction 108.


The resistive switching material 104 can include a suitable insulator material having a resistance that can be altered upon application of an electric field to the insulator material. In a specific embodiment, the resistive switching material 104 can include a silicon material. For example, the silicon material can be an amorphous silicon material, a microcrystalline silicon material, a macro crystalline silicon material, a silicon germanium material, a silicon oxide including any combination of these. In a various embodiments, the silicon material includes an amorphous silicon material and a silicon oxide material.


The resistive switching material 104 is characterized by a state, for example, a resistance state dependent on an electric field in the switching material. In a specific embodiment, the switching material is an amorphous silicon material. The amorphous silicon material has essentially intrinsic semiconductor characteristic and is not intentionally doped in a specific embodiment. In various embodiments, the amorphous silicon is also referred to as non-crystalline silicon (nc-Si). nc-Si non-volatile resistive switching devices may be fabricated using existing CMOS technologies. In an exemplary process, a mixture of silane (SiH4)(45 sccm) and Helium (He) (500 sccm) is used to form an a-Si layer with a deposition rate of 80 nm per minute (T=260° C., P=600 mTorr) during PECVD. In another exemplary process, a mixture of silane (SiH4)(190 sccm) and Helium (He) (100 sccm) is used to form an a-Si layer with a deposition rate of 2.8 A per second (T=380° C., P=2.2 Ton) during PECVD. In another exemplary process, silane (SiH4 80 sccm) or disilane is used to form an a-Si layer with a deposition rate of 2.8 mn per minute (T=585° C., P=100 mTorr) during LPCVD. Portions of poly-silicon grains may form during the LPCVD process and result in an amorphous-poly silicon film. In various embodiments, no p-type, n-type, or metallic impurities are intentionally added to the deposition chamber while forming the amorphous silicon material. Accordingly, when deposited, the amorphous silicon material is substantially free of any p-type, n-type or metallic dopants, i.e. the amorphous silicon material is undoped. A thin oxide may be formed above the amorphous silicon material, and be useful for switching purposes.


In yet another embodiment, the switching material 104, e.g. amorphous silicon material (and/or silicon oxide) 104 may be formed from an upper region of a p+ polycrystalline silicon or p+ silicon germanium bearing layer (e.g. 112) using an Argon, Silicon, Oxygen plasma etch, or the like. For instance, a plasma etch may use a bias power within a range of approximately 30 watts to approximately 120 watts to convert an upper region of the polysilicon or silicon germanium material into a non-conductive amorphous silicon having p-type impurities and/or a native silicon oxide (from the original polycrystalline silicon or silicon germanium bearing layer 112). In some embodiments, the silicon oxide may be SiOx, a sub-oxide. In some embodiments, switching layer may be on the order of 1 to 5 nm, e.g. 4 nm.


The second electrode 106 can be a second conductor material and can have a portion that includes a second metal material. The second metal material can be selected from aluminum, nickel, silver, gold, palladium, platinum, and others. The second metal material may have a suitable diffusivity in the switching material in a specific embodiment. In a specific embodiment, the second electrode is elongated in shape and configured to extend in a second direction 110 orthogonal to the first direction 108. In a specific embodiment, the second metal material includes a silver material.


As mentioned above, in certain embodiments, the resistive switching device 100 can include a contact material (112) disposed between the metal material of the first electrode 102 and the resistive switching layer 104. In some embodiments, the contact material 112 provides a suitable interfacial defect characteristic for desirable switching behavior for the switching device 100. For amorphous silicon material as the switching material 104, the contact material 112 can be p+ polysilicon or p+ silicon germanium material. In certain embodiments, the contact material 112 can be optional.


In various embodiments, additional interposing layer(s) 114 may be disposed between resistive switching material 104 and second electrode 106. The additional layer 114 may include a material that has non-noble metal properties, e.g. the material oxidizes in the presence of oxygen. In some examples, the additional layer 114 may be titanium, titanium nitride, tungsten, tungsten nitride, or the like. In various embodiments, additional layer 114 may serve as an adhesion and/or barrier layer between resistive switching material 104 and second electrode 106. In various embodiments, additional layer(s) 114 may be used to enhance retention, as will be described below. In some examples, the interposing layer is titanium/titanium oxide, and may be on the order of 1 to 5 nm, e.g. 2 nm.


In various embodiments, multiple resistive switching devices 100 can be disposed in an N by M crossbar array to form a high density interconnected array of non-volatile memory cells. A more detailed description of examples of a fabrication process are illustrated below.


As shown in FIG. 2, a semiconductor substrate 202 having a surface region 204 is provided. Semiconductor substrate 202 can be a single crystal silicon wafer, a silicon germanium material, a silicon on insulator (commonly called SOI) depending on the embodiment. In certain embodiments, semiconductor substrate 202 can have one or more MOS devices formed thereon or therein. The one or more MOS devices can be controlling circuitry for the resistive switching device, or the like in some embodiments.


In various embodiments, a processor, or the like, may include resistive memory memories as described herein. Because the resistive state-change memories are relatively non-volatile, the states of devices, such as processors, or the like may be maintained while power is not supplied to the processors. To a user, such capability would greatly enhance the power-on power-off performance of devices including such processors. Additionally, such capability would greatly reduce the power consumption of devices including such processors. In particular, because such resistive memories are non-volatile, the processor need not draw power to refresh the memory states, as is common with CMOS type memories. Accordingly, embodiments of the present invention are directed towards processors or other logic incorporating these memory devices, as described herein, devices (e.g. smart phones, network devices) incorporating such memory devices, and the like. Additionally, in various embodiments, multiple layers of memory cells (e.g. first and second conductors, resistive switching layers, etc. as illustrated in FIG. 1) may be fabricated in various embodiments, greatly increasing memory density for such processors, devices, or the like.


As illustrated in FIG. 3, embodiments of the method include depositing a first dielectric material 302 overlying the semiconductor substrate 202. First dielectric material 302 can be silicon oxide, silicon nitride, a dielectric stack of alternating layers of silicon oxide and silicon nitride (for example, an ONO stack), a low K dielectric, a high K dielectric, or a combination, and others, depending on the application. First dielectric material 302 can be deposited using techniques such as chemical vapor deposition, including low pressure chemical vapor deposition, plasma enhanced chemical vapor deposition, high density plasma chemical vapor deposition, atomic layer deposition (ALD), physical vapor deposition, including any combination of these, and others.


Referring to FIG. 4, embodiments of the method include depositing a first wiring material 402 overlying the first dielectric material. First wiring material 402 can be a suitable metal material including alloy materials, or a semiconductor material having a suitable conductivity characteristic. In some embodiments, the metal material can be tungsten, aluminum, copper or silver, and others. In some embodiments, the first wiring material may be a combination of conductive materials. In various embodiments, these metal materials may be deposited using a physical vapor deposition process, chemical vapor deposition process, electroplating, or electrodeless deposition process, a combinations of these, and others. In some embodiments, the semiconductor material can be, for example, a p-type doped silicon material, a conductive polysilicon, or the like.


In certain embodiments, a first adhesion material 404 is first formed overlying the first dielectric material 402 before deposition of the first wiring material 402 to promote adhesion of the first wiring material 402 to the first dielectric material 302. A diffusion barrier material 406 may also be formed overlying the first wiring material 402 to prevent, for example, the conductive material, the metal material, gasses, oxygen, or the like to contaminate other portions of the device in a specific embodiment.


In FIG. 5, an embodiment of the method subjects the first wiring material (302, 404 and 406) to a first pattern and etching process to form a first wiring structure 502 in a specific embodiment, while exposing a portion 504 of first dielectric material 302. As shown in FIG. 5, the first wiring structure 502 includes a plurality of first elongated structures configured to extend in a first direction 408 (into and out of the page) in a specific embodiment.


Referring to FIG. 6, a second dielectric material 602 is formed overlying the one or more first wiring structure and to fill a gap between the one or more first wiring structures 502 to isolate the one or more first wiring structures 502. Second dielectric material 602 further forms a thickness 604 overlying the first wiring structure 502 in a specific embodiment. Second dielectric material 602 can be silicon oxide, silicon nitride, silicon oxynitride, a high K dielectric, a low K dielectric, or a dielectric stack having alternating layer of silicon oxide and silicon nitride (for example an ONO stack), including any combination of these, and others. Second dielectric material 602 can be deposited using techniques such as chemical vapor deposition, including low pressure chemical vapor deposition, plasma enhanced chemical vapor deposition, high density plasma chemical vapor deposition, atomic layer deposition (ALD), physical vapor deposition, including any combination of these, and others.


In some embodiments, prior to forming second dielectric material 602 a thin layer of material may be deposited to protect the side walls of first wiring structure 502 from contaminants, such as oxygen. In some embodiments, titanium, titanium nitride, silicon nitride, or the like may be used.


In various embodiments, the second dielectric material 604 is subjected to a planarizing process to form a planarized dielectric surface 704 and to expose a surface region 706 of the first wiring structure 502, as shown in FIG. 7. Planarizing process can be a chemical mechanical polishing (CMP) process, or an etch back process, or a combination depending on the embodiment.


In a specific embodiment, a junction material 802 is deposited overlying the exposed surface region of the first wiring structure and the planarized surface of the second dielectric material, as illustrated in FIG. 8. Junction material 802 can be a p-doped silicon material. In a specific embodiment, the p-doped silicon material is a polysilicon having a p+ impurity characteristic. Depending on the application, the p+ impurity can be provided using boron, aluminum, gallium, indium, and other suitable p type impurity species. Again depending on the implementation, the polycrystalline silicon material may be deposited using techniques such as chemical vapor deposition including low pressure chemical vapor deposition, plasma enhanced chemical vapor deposition, atomic layer deposition, and others. Silicon precursors such as silane, a suitable chlorosilane in a presence of a reducing gas (for example, hydrogen) may be used. In other embodiments, the polycrystalline silicon material may be deposited using a physical vapor deposition technique from a suitable silicon target material. The p+ type impurity species can be co-deposited during deposition process (chemical vapor deposition or physical vapor deposition) or using an implantation process after deposition. Junction material 802 can be other suitable semiconductor material in a specific embodiment.


In various embodiments, the junction material 802 can be doped silicon germanium (poly-SiGe) material. In various embodiments, the silicon germanium material can be doped with a suitable impurity species to have a desirable conductivity, e.g. p+. The silicon germanium material can be deposited using a chemical vapor deposition process such as a low pressure chemical vapor deposition process, a plasma enhanced chemical vapor deposition process, atomic layer deposition (ALD) and others. Depending on the application, precursors such as silane and germane in a suitable carrier gas may be used. The silicon germanium material can have a p+ impurity characteristic provided by dopants such as boron, aluminum, gallium, indium, and others. Deposition temperature can range from about 400 Degree Celsius to about 490 Degree Celsius and the as deposited silicon germanium material is crystalline and has a desirable conductivity characteristic, without further anneal. Other deposition methods may also be used depending on the embodiment.


In various embodiments, as mentioned above, the junction material 802 may be composed of two or more layers of material. In one example, a highly doped layer of silicon bearing material may be disposed upon a lightly doped layer of silicon bearing material. These layers may be formed by increasing the dopant concentration during the formation of junction material 802. In some embodiments, an upper region may be a p+ silicon germanium layer, and a lower region may be a p− silicon germanium layer. It is believed that the upper region acts more like a conductor, and the lower region acts more like a resistive layer.


Depending on the application, a seed layer material may be formed overlying the first wiring material before deposition of the junction material. The seed layer material can include a thin layer of silicon material (about 40 Angstrom to about 120 Angstroms) deposited at temperatures no greater than about 430 Degree Celsius (for example, about 250 Degree Celsius to about 450 Degree Celsius) to promote crystallization of junction material 802.


As shown in FIG. 9, a hardmask material 902 is deposited overlying the junction material 802. Hardmask material 902 can be a dielectric material, for example, silicon oxide, silicon nitride, silicon oxynitride, alternating layers of silicon oxide and silicon nitride (for example, ONO) and others. Hardmask material and the junction material are subjected to a pattern and etch process 1000 to form a plurality of first structures 1002 as illustrated in FIG. 10. In various embodiments, each of the plurality of first structures 1002 is configured overlying and in electrical and physical contact with the first wiring structure, as shown.


Referring now to FIG. 11, the method includes depositing a third dielectric material 1102 overlying the plurality of first structures 1002 and filling a gap between each of the plurality of first structures 1002. The third dielectric material may be silicon oxide, silicon nitride, silicon oxynitride, and others. In certain implementations, third dielectric material is silicon oxide deposited using techniques such as chemical vapor deposition process, including plasma enhanced chemical vapor deposition process, low pressure chemical vapor deposition process, sub atmospheric chemical vapor deposition process, and others.


As seen in FIG. 12, in various embodiments, third dielectric material 1102 is then subjected to a planarizing process 1202 to expose a top surface region 1204 of the first structure 1002. Top surface region 1204 includes a top surface region of junction material 802 in a specific embodiment. Depending on the implementation, planarizing process 1202 can remove a portion of junction material 802. In some embodiments, deposition thickness of junction material 802 may have to account for the removal of the top surface region.


In a specific embodiment, the method includes forming a resistive switching material 1302 overlying top surface region of the first structure, including top surface region 1204 of junction material 802 and the exposed surface 1206 of third dielectric material 1102. Depending on the application, the top surface region 1204 of the junction material 802 may be subjecting to a cleaning step to remove contaminants from the planarizing process, and others.


In various embodiments, the resistive switching material 1302 includes an amorphous silicon material having an intrinsic semiconductor characteristic. The amorphous silicon material can be formed using a chemical vapor deposition process such as low pressure chemical vapor deposition process, plasma enhanced chemical vapor deposition process, and others. The chemical vapor deposition process can use silicon precursor such as silane, a suitable chlorosilane in presence of a reducing species (for example, hydrogen), and others. In some embodiments, the deposited amorphous silicon is not intentionally doped to maintain the intrinsic semiconductor characteristic during deposition or after deposition in a specific embodiment. Deposition temperature ranges from about 250 Degree Celsius to about 400 Degree Celsius depending on the implementation.


In other embodiments, as mentioned above, the top surface region 1204 of junction material 802 may be subject to a plasma cleaning/etching process using Argon, oxygen, or the like, for example. In some embodiments, this process may be useful for removing contaminants from the planarization process 1202. In some embodiments, the process also amorphizes an upper region of junction material 802. For example, the process changes a portion of a p+ silicon germanium region to a non-conductive amorphous region, including silicon, p type impurities, germanium, oxygen, and the like. In some examples, a silicon sub-oxide is formed. In some embodiments, this non-conductive amorphized layer may serve as the resistive switching material 1302. In various embodiments, the resistive switching material 1302 may only be formed overlying junction material 802.


Referring to FIG. 14, the method includes depositing an active metal material 1402 overlying the resistive switching material 1302. In various embodiments, when resistive switching material 1302 is amorphous silicon material, or the amorphized layer formed above, active metal material 1402 can be selected from silver, gold, palladium, platinum, aluminum, chromium, vanadium, and others. In some embodiments, the active metal material is selected to have a desirable diffusivity characteristic in resistive switching material 1302 in a presence of a suitable electric field.


In some embodiments, the active metal material 1402 is silver. Silver is sometimes deposited at a temperature no greater than about 250 Degree Celsius to inhibit mass diffusion of silver into the resistive switching material 1302. In some embodiments, a layer of titanium is deposited above resistive switching material 1302, prior to depositing active metal material 1402. In some embodiments, active metal material 1402 helps to protect resistive switching material 1302 from subsequent processing steps, or other variation.


In a specific embodiment, in operation, when a positive voltage greater than a threshold voltage applied to the active metal material 1402 with respect to the first wiring structure 502 causes the active metal material to migrate into a portion of the resistive switching layer 1302 to cause the material to change from a high resistance state into a low resistance state (or on state) and an on-state current flows.


As shown in FIG. 15, the method includes forming a second wiring material 1502 overlying active metal material 1402. Second wiring material 1502 can be copper, tungsten, or aluminum depending on the application. Depending on the implementation, the active metal material 1402 (for example, silver) may also serve as the second wiring material 1502. The second wiring material 1502 can further include one or more diffusion barrier layer material and/or adhesion materials to promote adhesion of the second wiring material 1502 to the second dielectric material 1206 and the active metal material 1402. The one or more diffusion barrier material and/or adhesion materials may further inhibit diffusion of the active metal material 1402 (e.g. silver) to prevent contamination to other parts of the device. Again depending on the implementation, the one or more diffusion barrier and/or adhesion materials can include titanium, titanium nitride, tungsten, titanium tungsten, tungsten, or a combination, and others.


In various embodiments, a diffusion barrier and/or adhesion material layer 1504 may be formed immediately after active metal material 1402 is deposited. This may be done, for example, in situ—within the same chamber, after active metal material 1402 (e.g. silver) is deposited, layer 1504 (e.g. titanium) is then deposited. Such embodiments may be useful to reduce the active metal material 1402 from contaminating subsequent processes, and/or may be useful to reduce undesirable changes to resistive switching material 1302. In some embodiments, this may be combined with a titanium layer (for example) being deposited immediately or close in time after resistive switching material 1302 is formed, and before active metal material 1402 is deposited.


In a specific embodiment, the method subjects a stack of material including the resistive switching material 1302, active metal material 1402, and second wiring material 1502 (including barrier and/or adhesion layers) to a third pattern and etch process 1602 to form a plurality of second structures 1604. Second structures 1604 including resistive switching material 1302, active metal material 1402, and second wiring material 1502 are typically configured to spatially extend in a second direction orthogonal to the first direction in certain embodiments.


In some embodiments wherein resistive switching material 1302 is formed as a result of an amorphizing etch (e.g. argon, oxygen), resistive switching material may be located at the intersections of second structures 1604 and first wiring structures 502.



FIGS. 17-20 illustrate various embodiments of a width of resistive switching material 1302 relative to pillar-like structure 1002, and for with regards to active metal material 1402. Briefly, in FIG. 17, a width of resistive switching material 1302 may be substantially similar to a width of active metal material 1402 and second wiring material 1502; in FIG. 18, a width of resistive switching material 1302 may be between a width of active metal material 1402 and a width of pillar-like structure 1002; in FIG. 19, a width of resistive switching material 1302 and a width of active metal material 1402 may be substantially similar but different from a width of pillar-like structure 1002; and in FIG. 20, a width of resistive switching material 1302 may be substantially similar to a width of pillar-like structure 1002. In light of the present disclosure, one of ordinary skill in the art will recognize that in other embodiments, other combinations and permutation of widths are also taught. In FIGS. 17-20, like references are used in the following and throughout the present disclosure and should not be construed to be limiting.


Referring to FIG. 17, a partial view of a resistive switching device 1700 according to various embodiments of the present invention is illustrated. Resistive switching device 1700 can be fabricated according to process steps as illustrated in FIGS. 2-16. As shown, resistive switching device 1700 includes first pillar-like structure 1002 comprising the junction material (for example, p+ polysilicon material; p+ polysilicon germanium material, or p+ SiGe/p-SiGe). First structure includes a first vertical region 1704. Resistive switching device 1700 further includes a second structure 1604. Second structure 1604 includes the resistive switching material 1302, active metal material 1402, and second wiring material configured as a stack of material, as shown. Second structure 1604 includes a common second vertical sidewall region 1702. As shown, first vertical sidewall region 1704 and second vertical sidewall region 1702 are free of a common vertical sidewall or a coincident vertical sidewall region. Contaminants 1706, especially conductive contaminants, on first vertical sidewall region 1704 or second vertical sidewall region 1702 may prevent an appropriate electrical connection between active metal material 1402 and the first wiring structure.


Depending on the implementation, there can be other variations. As shown in FIG. 18, the resistive switching material 1302 can form a resistive switching element 1802 overlying the first structure 1002. Resistive switching element 1802 is configured such that a second vertical side wall region 1804 is free from a common vertical side wall region with the first vertical side wall region 1704 associated with the junction material. Depending on the implementation, resistive switching element 1802 can be configured as a pillar structure having a cross sectional area no less than a cross sectional area of first structure 1704, as illustrated. Alternatively, resistive switching element 1802 can have a cross sectional area no greater than a cross sectional area of the first structure 1002. The method can form a dielectric material overlying resistive switching element 1802 to isolate the resistive switching elements 1802 in a specific embodiment. An active metal material 1402 is deposited overlying resistive switching material 1802 and a wiring material 1302 is deposited overlying the active metal material 1402. The method can form a structure from a second stack of material 1806 including the active metal material 1402 and the second wiring material 1502 in certain embodiments.


As shown in FIG. 19, the method can from a third structure 1904 including resistive switching material 1302 and active metal material 1402 overlying first structure 1002 associated with the junction material in another implementation. Third structure 1904 can be configured as a pillar structure in certain implementation. Again third structure 1904 is configured such that resistive switching material 1302 and junction material 1002 do not share a common side wall region or a coincident region, as shown in FIG. 19.


In a specific embodiment, a resistive switching device for a non-volatile memory device is provided. The resistive switching device includes a substrate having a surface region. In certain embodiments, the substrate can include one or more transistor device formed thereon. The one or more transistor device provides a circuitry for controlling operations of the resistive switching device. The resistive switching device includes a first dielectric material overlying the substrate and a first wiring structure overlying the first dielectric material. The first wiring structure can include a metal material or a semiconductor material configured to spatially extend in a first direction. The resistive switching device includes a first structure comprising a junction material overlying and in physical and electrical contact with the first wiring structure. In a specific embodiment, the first structure is configured as a pillar structure. The resistive switching device includes a second dielectric material filling the gaps between the first structures and isolate each of the first structures in certain implementation. The resistive switching device includes a second structure overlying the first structure. The second structure includes a stack of materials comprising a resistive switching material, an active metal material, and a second wiring material. In certain implementations, the first structure and the second structure are each elongated in shape and spatially configured perpendicular to each other. The active metal material, the resistive switching material, and the junction material form a resistive switching device in a specific embodiment. In certain implementation, the junction material includes a p+ polycrystalline silicon material. In another implementation, the junction material includes a p+ polycrystalline silicon germanium material. The resistive switching material includes an amorphous silicon material having an intrinsic semiconductor characteristic in a specific embodiment. For amorphous silicon as the resistive switching material, the active metal material can be selected from silver, gold, palladium, nickel, copper, aluminum, and others. The first structure and the second structure are configured such that the junction material and the resistive switching material are free from a common vertical side wall region. Depending on the application, the first wiring material and the second wiring material can each include a metal material and one or more diffusion barrier material. Alternatively, the first wiring material and the second wiring material can each include a doped semiconductor material.


Depending on the implementation, various device structures may be realized. For example, an alternative device structure can have a third structure including the resistive switching material overlying the first structure. The third structure and the first structure are free from a common vertical sidewall region, as shown in FIG. 18.


Yet alternatively, a fourth structure including the resistive switching material and the active metal material may be disposed overlying the first structure, wherein the resistive switching material and the junction material are free from a common sidewall region, as shown in FIG. 19. The second wiring structure is configured in a second direction orthogonal to the first direction of the first wiring structure.



FIG. 20 illustrates a resistive switching device where first side wall region 1702 associated with the resistive switching material 1302 shares a common side wall region with second sidewall region 1704 associated with junction material 1002. Contaminant material 2002 would cause electrical connection between second electrode 1402 and first electrodes 502 (not shown) rendering the device defective.


Though the present invention has been exemplified in various embodiments, it is to be understood that the examples and embodiment described herein are for illustrative purpose only and that various modifications or alternatives in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims.

Claims
  • 1. A method for forming a resistive switching device for a non-volatile memory device, comprising: providing a substrate having a surface region;forming a first dielectric layer overlying the surface region of the substrate;forming a first wiring structure comprising a first wiring material overlying the first dielectric layer;depositing a first junction material layer comprising a p+ polycrystalline silicon germanium containing material overlying at least the first wiring structure;depositing a hardmask material layer overlying the first junction material layer;subjecting the hardmask material layer and the first junction material layer to a first patterning and etching process to form one or more first structures overlying a surface region of the first wiring structure;forming a second dielectric layer to fill a gap region between the one or more first structures;forming a resistive switching material layer overlying the one or more first structures that comprises SiOx;depositing an active conductive material layer overlying the resistive switching material layer, wherein the resistive switching material layer is at least in part permeable to particles of the active conductive material layer that, in response to an electric field, facilitate formation of a conductive path through the resistive switching material layer;forming a second structure, overlying a first structure of the one or more first structures, from the resistive switching material layer and the active conductive material layer with one or more second patterning processes,wherein a first width of any two opposite first vertical sidewalls of the resistive switching material layer in the second structure is greater than a second width of any two opposite second vertical sidewalls of the first structure.
  • 2. The method of claim 1, wherein the first width of the resistive switching material layer in the second structure is substantially equal to a third width of two opposite third vertical sidewalls of the active conductive material layer in the second structure.
  • 3. The method of claim 1, wherein the first width of the resistive switching material layer in the second structure is less than a third width of two opposite third vertical sidewalls of the active conductive material layer in the second structure.
  • 4. The method of claim 3, wherein the resistive switching material layer in the second structure has a first vertical sidewall that is not coplanar with any third vertical sidewalls of the active conductive material layer in the second structure.
  • 5. The method of claim 1, wherein the resistive switching material layer in the second structure has a first vertical sidewall that is not coplanar with any second vertical sidewalls of the first structure.
  • 6. The method of claim 1, further comprising forming a second wiring structure comprising a second wiring material overlying the active conductive material layer; wherein a third width of two opposite third vertical sidewalls of the active conductive material layer in the second structure is less than a fourth width of two opposite fourth vertical sidewalls of the second wiring structure.
  • 7. The method of claim 1, further comprising depositing a barrier material layer overlying the active conductive material.
  • 8. The method of claim 7, wherein the barrier material layer is adjacent to the active conductive material layer.
  • 9. The method of claim 8, wherein the barrier material layer is selected from a group consisting of: titanium containing material, titanium nitride, titanium tungsten, titanium, tantalum, tantalum nitride, and tungsten nitride.
  • 10. The method of claim 8, wherein the barrier material layer comprises a metal material comprising copper.
  • 11. The method of claim 1, wherein the active conductive material layer is selected from a group consisting of: silver, gold, and aluminum.
  • 12. A method for forming a semiconductor device, comprising: providing a substrate;forming a first dielectric layer overlying the substrate;forming a first wiring structure comprising a first wiring metal overlying the first dielectric layer;forming a second dielectric layer overlying filling gaps in the surface region of the first wiring structure while leaving a first surface region of the first wiring structure exposed;forming a structure comprising a junction material layer overlying the first surface region of the first wiring structure;forming a resistive switching material layer overlying at least a portion of the second dielectric layer and the structure, wherein the resistive switching material comprises a silicon sub-oxide; anddepositing an active conductive material layer overlying the resistive switching material layer, wherein the active conductive material layer is configured to provide particles that form a conductive path through at least a portion of the resistive switching material layer in response to an electric field;patterning the active conductive material layer and the resistive switching material layer to form a pillar-like memory stack overlying the structure, wherein a first width of any two opposite first vertical sidewalls of the pillar-like memory stack is greater than a second width of any two opposite second vertical sidewalls of the structure; andforming a second wiring structure comprising a second wiring metal overlying the pillar-like memory stack.
  • 13. The method of claim 12, wherein the active conductive material layer is selected from a group consisting of: silver, gold and aluminum.
  • 14. The method of claim 12, wherein the second wiring metal is selected from a group consisting of: copper, tungsten, and aluminum.
  • 15. The method of claim 14, further comprising depositing a barrier material layer overlying the active conductive material layer, wherein the barrier material layer is selected from a group consisting of: titanium containing material, titanium nitride, titanium tungsten, titanium, tantalum, tantalum nitride, and tungsten nitride.
  • 16. The method of claim 12, wherein the junction material layer comprises a doped polycrystalline silicon germanium material.
  • 17. The method of claim 12, wherein a third width of two opposite third vertical sidewalls of the resistive switching material layer in the pillar-like memory stack is substantially equal to a fourth width of two opposite fourth vertical sidewalls of the active conductive material layer in the second structure.
  • 18. The method of claim 12, wherein a third width of two opposite third vertical sidewalls of the resistive switching material layer in the pillar-like memory stack is less than a fourth width of two opposite fourth vertical sidewalls of the active conductive material layer in the second structure.
  • 19. The method of claim 12, wherein the pillar-like memory stack comprises a resistive switching device; andwherein the substrate includes one or more MOS devices; andwherein the one or more MOS devices are selected from a group consisting: processing circuitry, control circuitry for the resistive switching device, and logic circuitry.
  • 20. The method of claim 19, wherein at least one of the one or more MOS devices are coupled to the resistive switching device.
US Referenced Citations (249)
Number Name Date Kind
680652 Elden Aug 1901 A
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
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
8004882 Katti et al. Aug 2011 B2
8018760 Muraoka et al. Sep 2011 B2
8021897 Sills et al. Sep 2011 B2
8030634 Lung et al. Oct 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
8207064 Bandyopadhyay et al. Jun 2012 B2
8227787 Kumar et al. Jul 2012 B2
8233308 Schricker et al. Jul 2012 B2
8237146 Kreupl et al. Aug 2012 B2
8265136 Hong et al. Sep 2012 B2
8374018 Lu Feb 2013 B2
8385100 Kau et al. Feb 2013 B2
8394670 Herner Mar 2013 B2
8467227 Jo Jun 2013 B1
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
20040202041 Hidenori Oct 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
20060134837 Subramanian et al. Jun 2006 A1
20060246606 Hsu et al. Nov 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
20100032637 Kinoshita et al. Feb 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
20110186797 Herner Aug 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
20120170359 Wu et al. Jul 2012 A1
20120205606 Lee et al. Aug 2012 A1
20120220100 Herner Aug 2012 A1
20120235106 Tang Sep 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
20130134383 Hwang et al. May 2013 A1
Foreign Referenced Citations (8)
Number Date Country
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
1020110014248 Feb 2011 KR
WO 03034498 Apr 2003 WO
WO 2009005699 Jan 2009 WO
Non-Patent Literature Citations (152)
Entry
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. 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.
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.
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.
Jian Hu et al., “Area-Dependent Switching in Thin Film-Silicon Devices”, Materials Research Society, Mal. Res. Soc. Symp Proc., 2003, pp. A18.3.1-A18.3.6, vol. 762.
Andrédehon, “Array-Based Architecture for FET-Based, Nanoscale Electronics”, IEEE Transactions on Nanotechnology, Mar. 2003, pp. 23-32, vol. 2, No. 1, IEEE.
Herb Goronkin et al., “High-Performance Emerging Solid-State Memory Technologies”, MRS Bulletin, www.mrs.org/publications/bulletin, Nov. 2004, pp. 805-813.
Gerhard Müller 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/Physical Society of Japan.
J. Campbell Scott, “Is There an Immortal Memory?”, www.sciencemag.org, Apr. 2, 2004, pp. 62-63, vol. 304 No. 5667, American Association for the Advancement of Science.
S.H. Lee et al., “Full Integration and Cell Characteristics for 64Mb Nonvolatile PRAM”, 2004 Symposium on VLSI Technology Digest of Technical Papers, IEEE, 2004, pp. 20-21.
Stephen Y. Chou et al., “Imprint Lithography With 25-Nanometer Resolution”, Science, Apr. 5, 1996, pp. 85-87, vol. 272, American Association for the Advancement of Science.
S. Zankovych et al., “Nanoimprint Lithography: challenges and prospects”, Nanotechnology, 2001, pp. 91-95, vol. 12, Institute of Physics Publishing.
A. Avila et al., “Switching in coplanar amorphous hydrogenated silicon devices”, Solid-State Electronics, 2000, pp. 17-27, vol. 44, Elsevier Science Ltd.
Jian Hu et al., “Switching and filament formation in hot-wire CVD p-type a-Si:H devices”, Thin Solid Films, Science Direct, www.sciencedirect.com, 2003, pp. 249-252, vol. 430, Elsevier Science B.V.
S. Hudgens et al., “Overview of Phase-Change Chalcogenide Nonvolatile Memory Technology”, MRS Bulletin, www.mrs.org/publications/bulletin, Nov. 2004, pp. 829-832.
K. Terabe et al., “Quantized conductance atomic switch”, Nature, www.nature.com/nature, Jan. 6, 2005, pp. 47-50, vol. 433, Nature Publishing Group.
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”, Appl. Phys. Letter, 1982, pp. 812-813, vol. 40, American Institute of Physics.
P.G. Lecomber et al., “The Switching Mechanism in Amorphous Silicon Junctions”, Journal of Non-Crystalline Solids, 1985, pp. 1373-1382, vol. 77 & 78, Elsevier Science Publishers B.V., North Holland Physics Publishing Division, North-Holland, Amsterdam.
A. E. Owen et al., “Switching in amorphous devices”, Int. J. Electronics, 1992, pp. 897-906, vol. 73, No. 5, Taylor and Francis Ltd.
M. Jafar et al., “Switching in amorphous-silicon devices”, Physical Review B, May 15, 1994, pp. 611-615, vol. 49, No. 19, The American Physical Society.
Alexandra Stikeman, “Polymer Memory—The plastic path to better data storage”, Technology Review, www.technologyreview.com, Sep. 2002, pp. 31.
Yong Chen et al., “Nanoscale molecular-switch crossbar circuits”, Nanotechnology, 2003, pp. 462-468, vol. 14, Institute of Physics Publishing Ltd.
C. P. Collier et al., “Electronically Configurable Molecular-Based Logic Gates”, Science Jul. 16, 1999, pp. 391-395, vol. 285, No. 5426, American Association for the Advancement of Science.
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.
Jang Wook Choi, “Bistable [2]Rotaxane Based Molecular Electronics: Fundamentals and Applications”, Dissertation, Chapter 3, <http://resolver.caltech.edu/CaltechETD:etd-05242007-194737> 2007, pp. 79-120, California Institute of Technology, Pasadena.
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.
Rainer Waser et al., “Nanoionics-based resistive switching memories”, Nature Materials, Nov. 2007, pp. 833-835, vol. 6, Nature Publishing Group.
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 Allowance 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 Allowance 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”, IEEE, 2008.
Sung Hyun Jo et al., “Nanoscale Memristor Device as Synapse in Neuromorphic Systems”, Nano Letters, 10, 1297-1301, 2010, pubs.acs.org/NanoLett, A-E, American Chemical Society Publications.
Wei Lu et al., “Nanoelectronics from the bottom up”, Nature Materials, 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”, Nanotechnology Materials and Devices Conference, IEEE, 2006, pp. 116-117, vol. 1.
Sung Hyun Jo et al., “Experimental, Modeling and Simulation Studies of Nanoscale Resistance Switching Devices”, 9th Conference on Nanotechnology, IEEE, 2009, pp. 493-495.
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”, Proceedings of 2010 IEEE International Symposium on Circuits and Systems, 2010, pp. 13-16.
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 Two-Terminal 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.
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, 1989, pp. 168-170, vol. 115, Elsevier Science Publishers B.V., North-Holland.
A. Moopenn et al., “Programmable Synaptic Devices for Electronic Neural Nets”, Control and Computers, 1990, pp. 37-41, vol. 18 No. 2.
P.G. Le Comber, “Present and Future Applications of Amorphous Silicon and Its Alloys”, Journal of Non-Crystalline Solids, 1989, pp. 1-13, vol. 115, Elsevier Science Publishers B.V., North-Holland.
J. Hu, et al., “AC Characteristics of Cr/p+a-Si:H/V Analog Switching Devices”, IEEE Transactions on Electron Devices, Sep. 2000, pp. 1751-1757, vol. 47 No. 9, IEEE.
A.E. Owen et al., “New amorphous-silicon electrically programmable nonvolatile switching device”, Solid-State and Electron Devices, IEEE Proceedings, Apr. 1982, pp. 51-54, vol. 129, Pt. I., 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.
Yajie Dong et al., “Si/a-Si Core/Shell Nanowires as Nonvolatile Crossbar Switches”, Nano Letters, Jan. 2008, pp. 386-391, vol. 8 No. 2, American Chemical Society.
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. 24, 1999, pp. 758-761, vol. 399.
J. Suñéet al., “Nondestructive multiple breakdown events in very thin SiO2 films”, Applied Physics Letters, 1989, pp. 128-130, vol. 55.
Herve Marand et al., MESc. 5025 lecture notes: Chapter 7. Diffusion, University of Vermont, http://www.files.chem.vt.edu/chem-dept/marand/MEScchap6-1c.pdf.
A. E. Owen et al., “Electronic Switching in Amorphous Silicon Devices: Properties of the Conducting Filament”, Proceedings of 5th International Conference on Solid-State and Integrated Circuit Technology, IEEE, 1998, pp. 830-833.
Sung Hyun Jo, “Nanoscale Memristive Devices for Memory and Logic Applications”, Ph. D dissertation, University of Michigan, 2010.
Office Action for U.S. Appl. No. 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.
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.
Office Action for U.S. Appl. No. 12/814,410 dated Apr. 17, 2012.
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. Lett., 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 Junctions 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 dated 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.