Precessional spin current magnetic tunnel junction devices and methods of manufacture

Information

  • Patent Grant
  • 10784439
  • Patent Number
    10,784,439
  • Date Filed
    Friday, December 29, 2017
    7 years ago
  • Date Issued
    Tuesday, September 22, 2020
    4 years ago
Abstract
A Magnetic Tunnel Junction (MTJ) device can include a second Precessional Spin Current (PSC) magnetic layer of Ruthenium (Re) having a predetermined thickness and a predetermined smoothness. An etching process for smoothing the PSC magnetic layer can be performed in-situ with various deposition processes after a high temperature annealing of the MTJ formation.
Description
BACKGROUND OF THE INVENTION

Computing systems have made significant contributions toward the advancement of modern society and are utilized in a number of applications to achieve advantageous results. Numerous devices, such as desktop personal computers (PCs), laptop PCs, tablet PCs, netbooks, smart phones, game consoles, servers, distributed computing systems, and the like have facilitated increased productivity and reduced costs in communicating and analyzing data in most areas of entertainment, education, business, and science. One common aspect of computing systems is the computing device readable memory. Computing devices may include one or more types of memory, such as volatile random-access memory, non-volatile flash memory, and the like.


An emerging non-volatile memory technology is Magnetoresistive Random Access Memory (MRAM). In MRAM devices, data can be stored in the magnetization orientation between ferromagnetic layers of a Magnetic Tunnel Junction (MTJ). Referring to FIGS. 1A and 1B, a simplified diagram of a MTJ, in accordance with the convention art, is shown. The MTJ can include two magnetic layers 110, 120, and a magnetic tunnel barrier layer 130. One of the magnetic layers 110 can have a fixed magnetization polarization 140, while the polarization of the magnetization of the other magnetic layer 120 can switch between opposite directions 150, 160. Typically, if the magnetic layers have the same magnetization polarization 140, 150, the MTJ cell will exhibit a relatively low resistance value corresponding to a ‘1’ bit state; while if the magnetization polarization between the two magnetic layers is antiparallel 140, 160 the MTJ cell will exhibit a relatively high resistance value corresponding to a ‘0’ bit state. Because the data is stored in the magnetic fields, MRAM devices are non-volatile memory devices. The state of a MRAM cell can be read by applying a predetermined current through the cell and measuring the resulting voltage, or by applying a predetermined voltage across the cell and measuring the resulting current. The sensed current or voltage is proportional to the resistance of the cell and can be compared to a reference value to determine the state of the cell.


MRAM devices are characterized by densities similar to Dynamic Random-Access Memory (DRAM), power consumption similar to flash memory, and speed similar to Static Random-Access Memory (SRAM). Although MRAM devices exhibit favorable performance characteristics as compared to other memory technologies, there is a continuing need for improved MRAM devices and methods of manufacture thereof.


SUMMARY OF THE INVENTION

The present technology may best be understood by referring to the following description and accompanying drawings that are used to illustrate embodiments of the present technology directed toward Precessional Spin Current (PSC) Magnetic Tunnel Junction (MTJ) devices, improvement to Magnetic Anisotropies in MTJ devices and method of manufacture thereof.


In one embodiment, a PSC MTJ device can include one or more seed layers disposed on a substrate, a Synthetic Antiferromagnetic (SAF) formation disposed on the one or more seed layers, a MTJ formation disposed on the SAF formation, a PSC coupling layer or Perpendicular Magnetic Anisotropy (PMA) enhancement layer disposed on the MTJ formation, a first PSC magnetic layer disposed on the PSC coupling or PMA enhancement layer, and a second PSC magnetic layer disposed on the first PSC magnetic layer. The second PSC magnetic layer can have a thickness of approximately 1.5 nm and a smoothness of approximately 0.2 nm. The PSC MTJ device can further include a third PSC magnetic layer disposed on the second PSC magnetic layer, and a capping layer disposed on the third PSC magnetic layer.


In one embodiment, a method of fabricating the PSC MTJ device can include depositing the second PSC magnetic layer on the first PSC magnetic layer, wherein the second PSC magnetic layer includes Ruthenium (Ru) and the first PSC magnetic layer includes Iron (Fe). The optional intermediate capping layer can be deposited on the second PSC magnetic layer, wherein the intermediate capping layer includes Tantalum (Ta). The first and second PSC magnetic layers, and the optional intermediate capping layer, can be deposited in a first vacuum condition. Optionally, the MTJ formation can be subject to a high temperature annealing process after deposition of the first and second PSC magnetic layers and the optional intermediate capping layer if applicable. The second PSC magnetic layer, and the optional intermediate capping layer if applicable, can be etched by a two-step etching process. At least a portion of the second PSC magnetic layer can be subjected to a slow etch portion of the two-step etching process to smooth the surface of the second PSC magnetic layer. The third PSC magnetic layer can be deposited on the second PSC magnetic layer after the slow etch of the second PSC magnetic layer, wherein the third PSC magnetic layer includes ferromagnetic materials, for instance one or more of Cobalt (Co), Iron (Fe) and Boron (B). The optional capping layer can be deposited on the third magnetic layer. The two-step etching process and the deposition of the third PSC magnetic layer, and optional capping layer if applicable, can be performed in a second vacuum condition.


In another embodiment, a method of fabricating the PSC MTJ device can include receiving a wafer including a first Precessional Spin Current (PSC) magnetic layer disposed on a MTJ formation and a second PSC magnetic layer disposed on the first PSC magnetic. The first PSC magnetic layer can include Iron (Fe) and the second PSC magnetic layer can include Ruthenium (Ru). In a two-step etching process, at least a first portion of the second PSC magnetic layer can be etched with a fast etch process to remove the first portion of the second PSC magnetic layer. At least a second portion of the second PSC magnetic layer can be etched with a slow etch process to smooth the surface of the Ruthenium (Ru) of the second PSC magnetic layer as deposited. A third PSC magnetic layer can be deposited on the second PSC magnetic layer after the slow etch of the second PSC magnetic layer. The third PSC magnetic layer can include one or more of Cobalt (Co), Iron (Fe) and Boron (B). A capping layer can be deposited on the third magnetic layer.


This Summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter.





BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the present technology are illustrated by way of example and not by way of limitation, in the figures of the accompanying drawings and in which like reference numerals refer to similar elements and in which:



FIGS. 1A and 1B show a simplified diagram of a Magnetic Tunnel Junction (MTJ), in accordance with the convention art.



FIG. 2 shows a block diagram of a Precessional Spin Current (PSC) MTJ device, in accordance with embodiments of the present technology.



FIGS. 3A-3C show a block diagram illustrating fabrication of one or more PSC layers of a MTJ device, in accordance with embodiments of the present technology.



FIG. 4 shows a block diagram of an Interface Perpendicular Magnetic Anisotropies (IMPA) improved MTJ device, in accordance with embodiments of the present technology.



FIGS. 5A-5C show a block diagram illustrating fabrication of an IMPA improved MTJ device, in accordance with embodiments of the present technology.



FIG. 6 shows a block diagram of a Magnetoresistive Random Access Memory (MRAM), in accordance with embodiments of the present technology.



FIG. 7 shows a circuit diagram of a MRAM memory cell array, in accordance with the conventional art.





DETAILED DESCRIPTION OF THE INVENTION

Reference will now be made in detail to the embodiments of the present technology, examples of which are illustrated in the accompanying drawings. While the present technology will be described in conjunction with these embodiments, it will be understood that they are not intended to limit the invention to these embodiments. On the contrary, the invention is intended to cover alternatives, modifications and equivalents, which may be included within the scope of the invention as defined by the appended claims. Furthermore, in the following detailed description of the present technology, numerous specific details are set forth in order to provide a thorough understanding of the present technology. However, it is understood that the present technology may be practiced without these specific details. In other instances, well-known methods, procedures, components, and circuits have not been described in detail as not to unnecessarily obscure aspects of the present technology.


Some embodiments of the present technology which follow are presented in terms of routines, modules, logic blocks, and other symbolic representations of operations on data within one or more electronic devices. The descriptions and representations are the means used by those skilled in the art to most effectively convey the substance of their work to others skilled in the art. A routine, module, logic block and/or the like, is herein, and generally, conceived to be a self-consistent sequence of processes or instructions leading to a desired result. The processes are those including physical manipulations of physical quantities. Usually, though not necessarily, these physical manipulations take the form of electric or magnetic signals capable of being stored, transferred, compared and otherwise manipulated in an electronic device. For reasons of convenience, and with reference to common usage, these signals are referred to as data, bits, values, elements, symbols, characters, terms, numbers, strings, and/or the like with reference to embodiments of the present technology.


It should be borne in mind, however, that all of these terms are to be interpreted as referencing physical manipulations and quantities and are merely convenient labels and are to be interpreted further in view of terms commonly used in the art. Unless specifically stated otherwise as apparent from the following discussion, it is understood that through discussions of the present technology, discussions utilizing the terms such as “receiving,” and/or the like, refer to the actions and processes of an electronic device such as an electronic computing device that manipulates and transforms data. The data is represented as physical (e.g., electronic) quantities within the electronic device's logic circuits, registers, memories and/or the like, and is transformed into other data similarly represented as physical quantities within the electronic device.


In this application, the use of the disjunctive is intended to include the conjunctive. The use of definite or indefinite articles is not intended to indicate cardinality. In particular, a reference to “the” object or “a” object is intended to denote also one of a possible plurality of such objects. It is also to be understood that the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting.


Referring to FIG. 2, a block diagram of a Precessional Spin Current (PSC) Magnetic Tunnel Junction (MTJ) device, in accordance with embodiments of the present technology, is shown. The PSC MTJ 200 can include one or more seed layers 205 disposed on a substrate 210. The one or more seed layers 205 can be deposited on the substrate 210 to initiate a predetermined crystalline growth in one or more subsequent deposited layers. In one implementation, the one or more seed layers 205 can include one or more layers of Tantalum (Ta), Tantalum Nitride (TaN), Chromium (Cr), Copper (Cu), Copper Nitride (CuN), Nickel (Ni), Iron (Fe), Platinum (Pt), Cobalt (Co) or alloys thereof with a thickness of approximately 1-20 nanometers (nm).


In one aspect, a Synthetic Antiferromagnetic (SAF) formation 215-225 can be disposed on the one or more seed layers 205. In one implementation, the SAF formation 215-225 can including a first ferromagnetic layer 215 disposed on the one or more seed layers 205, a first non-magnetic layer 220 disposed on the first ferromagnetic layer 215, and a second ferromagnetic layer 225 disposed on the first non-magnetic layer 220. The first ferromagnetic layer 215 can be a Cobalt (Co), Cobalt Nickel (CoNi), or Cobalt Platinum (CoPt) alloy with a thickness of approximately 1-5 nm, the first non-magnetic layer 220 can be a Ruthenium (Ru) metal with a thickness of approximately 0.9 nm the second ferromagnetic layer 225 can be a Cobalt (Co), Cobalt Nickel (CoNi), Cobalt Platinum (CoPt) and/or Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 2.3 nm.


In one aspect, a MTJ formation 225-235 can be disposed on the SAF formation 215-225. In one aspect, the MTJ formation 225-235 can share one or more layers in common with the SAF formation 215-225. In one implementation, the MTJ formation 225-235 can include a reference magnetic layer 225, a non-magnetic tunneling barrier layer 230, and a free magnetic layer 235. The reference magnetic layer 225 and the second ferromagnetic layer 225 can be the same layer of Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 1-5 nm. For ease of explanation, where the second ferromagnetic layer 225 and the reference magnetic layer 225 are the same layer, the combined layer will be referred to as the reference magnetic layer 225. The non-magnetic tunneling barrier layer 230 can be a Magnesium (Mg) oxide of approximately 1-10 nm, and the free magnetic layer 235 can be a Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 2.3 nm. The reference magnetic layer 225 can have its magnetization pinned in a predetermined direction, meaning that the reference magnetic layer 225 has a higher coercivity than other layers and a larger magnetic field or spin-polarized current is needed to change the orientation of its magnetization. The magnetization direction of the free magnetic layer 235 can be changed by a smaller magnetic field or sin-polarized current relative to the reference magnetic layer 225.


In one aspect, the magnetization vector of the first ferromagnetic layer 215 and the reference magnetic layer 225 can be substantially perpendicular (e.g., within several degrees) to a plane of the layers (e.g., along a z-axis). The magnetization vector of the free magnetic layer 235 can also be substantially perpendicular to the plane of the layer (e.g., along a z-axis), but its direction can vary by 180 degrees.


In one aspect, a PSC coupling and/or Perpendicular Magnetic Anisotropy (PMA) enhancement layer 240 can be disposed on the MTJ formation 225-235. One or more PSC magnetic layers 245, 250, 265 can be disposed on the PSC coupling and/or PMA enhancement layer 240. In one implementation, the PSC coupling and/or PMA enhancement layer 240 can be a non-magnetic material such as Ruthenium (Ru), Tantalum (Ta), Tantalum Nitride (TaN), Copper (Cu), Copper Nitride (CuN), or Magnesium Oxide (MgO) with a thickness of approximately 1-10 nm. In one embodiment, the one or more PSC magnetic layers 245, 250 can include a first PSC magnetic layer 245 disposed on the PSC coupling and/or PMA enhancement layer 240, a second PSC magnetic layer 250 disposed on the first PSC magnetic layer 245, and a third PSC magnetic layer 265 disposed on the second PSC magnetic layer 250. In one implementation the first PSC magnetic layer 245 can be iron (Fe) with a thickness of approximately 0.6 nm, the second PSC magnetic layer 250 can be ruthenium (Ru) with a thickness of approximately 1.5 nm, and the third PSC magnetic layer 265 can be a cobalt-iron-boron (Co—Fe—B) alloy with a thickness of approximately 1.85 nm.


In one aspect, the one or more PSC magnetic layers 245, 250, 265 have a low coercivity and therefore are typically manufacture using a very soft magnetic material (e.g., less than fifty (50) Oersteds). In one implementation, the one or more PSC magnetic layers 245, 250, 265 have a magnetization vector having a direction substantially parallel to the plane of the layer (e.g., within a plane of the x-y axes), and orthogonal to the magnetization direction of the free magnetic layer 235. In another implementation, the magnetization direction of the one or more PSC magnetic layers 245, 250, 265 can have a horizontal component X and a perpendicular component Z, such that an angle θ between the plane of the free magnetic layer 235 and the magnetic direction of the one or more PSC magnetic layers 245, 250, 265 can be between 0-90 degrees.


In one aspect, a PSC coupling layer 240 can be configured to promote electromagnetic coupling between the one or more PSC magnetic layers 245, 250, 265 and the free magnetic layer 235, such that the magnetic direction of the one or more PSC magnetic layers 245, 250, 265 follow the precession cycle of the free magnetic layer 235. The PSC coupling layer 240 can also be configured to transmit spin current efficiently from the one or more PSC magnetic layers 245, 250, 265 into the free magnetic layer 235. The PSC coupling layer 240 can also be configured to promote good microstructure and high tunneling magnetoresistance (TMR. In one aspect, the one or more PSC magnetic layers 245, 250, 265 are free to rotate near the same frequency as the precessional motion of the free magnetic layer 235. By having nearly the same frequency of magnetization rotations, the free magnetic layer 235 switching time can be significantly reduced and the thermal distribution of the switching times can be tightened. The one or more PSC magnetic layers 245, 250, 265 can also have a rotational frequency greater than zero. The one or more PSC magnetic layers 245, 250, 265 can also have a circular or near circular shape so that its magnetization direction has substantially no shape induced anisotropy in the plane (e.g., the x-y plane). In one aspect, a PMA enhancement layer 240 can be configured to control magnetic anisotropy and free layer magnetization.


Referring now to FIGS. 3A-3C, a block diagram illustrating fabrication of one or more PSC layers of a Magnetic Tunnel Junction (MTJ), in accordance with embodiments of the present technology, is shown. The processes of forming the seed layer 205 on the substrate 210, the SAF formation 215-225 on the seed layer 205, the MTJ formation 225-235 on the SAF formation 215-225, and the PSC coupling and/or PMA enhancement layer 240 on the MTJ formation 225-235 are well known in the art and are not germane to understanding embodiments of the present technology, and therefore will not be described in further detail herein.


Fabrication of the PSC MTJ after deposition of the PSC coupling and/or PMA enhancement layer 240 can continue with deposition of the first PSC magnetic layer 245. In one aspect, a first PSC magnetic layer 245 of Iron (Fe) can be deposited on the PSC coupling and/or PMA enhancement layer 240. In one implementation, the Iron (Fe) can be deposited using a sputtering, vapor deposition, or similar process. The Iron layer can be deposited to a thickness of approximately 0.6 nm. In one aspect, a second PSC magnetic layer 250 of Ruthenium (Ru) can be deposited on the first PSC magnetic layer 245. In one implementation, the Ruthenium (Ru) can be deposited using a sputtering, vapor deposition, or similar process. The Ruthenium (Ru) can be deposited to a thickness of approximately 2-10 nm. The combination of the PSC coupling and/or PMA enhancement layer 240 and the first and second PSC magnetic layers 245, 250 form and intermediate capping formation. The thickness of the Ruthenium (Ru) can protect the MTJ formation 225-235 from contamination by an ambient environment. In one implementation, the thickness of the Ruthenium (Ru) can protect the MTJ formation 225-235 from oxidation. In one aspect, additional intermediate capping layers 255 can optionally be deposited for additional protection against contamination. In one implementation, an additional intermediate capping layer 255 of Tantalum (Ta) can be deposited on second PSC magnetic layer 250. If the additional intermediate capping layer 255 is used, the thickness of the Ruthenium (Ru) of the second PSC magnetic layer 250 can be reduced to decrease a subsequent etching time. The structure, as fabricate up to this point, can then be exposed to an ambient environment for further processing.


In one aspect, the PSC MTJ can be subject to a two stage-etching process 260 after deposition of the second PSC magnetic layer 250, and after the optional intermediate capping layer 255 if included, as illustrated in FIG. 3A. The two-stage etching process can include a first etch to remove the intermediate capping layer 255 or a portion thereof if included, and optionally a portion of the second PSC magnetic layer 250 at a first rate. A first etch can be performed using Argon (Ar) or Krypton (Kr) plasma etching at the fast rate of approximately 5-20 sec/nanometer and 100-500 Watts power. A second etch can be used to optionally remove another portion of the intermediate capping layer 255 and remove a portion of the PSC magnetic layer 250 at a second slow rate of approximately 60-120 sec/nanometer and 20-100 Watts, as illustrated in FIG. 3B. In one implementation, the second etching process can be performed until the Ruthenium (Ru) of the second PSC coupling layer 250 is thinned to approximate 1-3 nm. The second etching rate can be slower than the first etching rate. In one implementation, the slower second etching rate can smooth the surface of the second PSC magnetic layer 250 as compared to the surface of the PSC magnetic layer 250 as deposited. Smoothing the surface of the second PSC magnetic layer 250 can improve the Precessional Spin Current (PSC) effect by additional control of the coupling mechanism and spin transport enhancement within PSC layers.


In one aspect, a third PSC magnetic layer 265 of Cobalt-Iron-Boron (Co—Fe—B) can be deposited on the second PSC magnetic layer 250 of Ruthenium (Ru) after the two-stage etching process 260. In one implementation, the Cobalt-Iron-Boron (Co—Fe—B) can be deposited using a sputtering, vapor deposition, or similar process. The Cobalt-Iron-Boron (Co—Fe—B) can be deposited to a thickness of approximately 1.85 nm. In one aspect, one or more capping layers 270 can be deposited on the third PSC magnetic layer 265. In one aspect, the two-stage etching process 260, the third PSC magnetic layer 265 deposition, and the one or more capping layer 270 depositions can be performed in-situ without breaking a vacuum of the fabrication equipment used to perform the etching and deposition processes.


In another embodiment, the PSC MTJ fabricated with the Ruthenium (Ru) second PSC magnetic layer 250 and optional intermediate capping layer 255, can be exposed to an ambient environment for transferring to an annealing process. In one aspect, a high temperature annealing process can be configured to enhance performance of the MTJ formation 225-235. In one implementation, a high temperature annealing process can be performed after deposition of the second PSC magnetic layer 250, and the optional intermediate capping layer 255, if used. The second PSC magnetic layer 250, and the optional intermediate capping layer 255 protect the MTJ formation 225-235 from the ambient prior to, during and after annealing. By being able to perform the high temperature annealing after deposition of the second PSC magnetic layer 250, and the optional intermediate capping layer 255, other materials that may be adversely affected by a high-temperature anneal can be utilized in the third PSC magnetic layer 265, and the one or more capping layers 270. In another implementation, the high temperature annealing process can be performed after deposition of the third PSC magnetic layer 265 and the capping layer 270. In one aspect, the two-step etching process 260, the third PSC magnetic layer 265 and the one or more capping layer 270 may not be sensitive to changes due to high temperature annealing. In such case, the high-temperature annealing process utilized for the SAF formation and/or MTJ formation can be performed after the third PSC magnetic layer 265 and the one or more capping layers 270 are deposited. If, however, the materials of the third PSC magnetic layer 265 and/or the one or more capping layer 270 are sensitive to changes due to high temperature annealing, the annealing can be performed after deposition of the second PSC magnetic layer 250 and intermediary capping layer 255.


In one implementation, one or more seed layers 205, the SAF formation 215-225, the MTJ formation 225-235, the optional PSC coupling layer or PMA enhancement layer 240, the first and second PSC magnetic layers 245, 250, and the optional intermediate capping layer 255 can be manufactured by a first entity. Thereafter, the partially fabricated PSC MTJ device can exposed to an ambient environment for transferring to an annealing process. Fabrication can then proceed with in-situ etching to remove the optional intermediate capping layer 255, smoothing the second PSC magnetic layer 245, and forming the third PSC coupling layer 265 and capping layer 270. In another implementation, the partially fabricated PSC MTJ device can exposed to an ambient environment for transferring to a second entity. The second entity can thereafter, proceed with in-situ etching to remove the optional intermediate capping layer 255, smoothing the second PSC magnetic layer 245, and forming the third PSC coupling layer 265 and capping layer 270. Furthermore, an annealing process can be performed by either entity after formation of the second PSC magnetic layer 250 and the optional intermediate capping layer 255.


Referring now to FIG. 4, a block diagram of an Interface Perpendicular Magnetic Anisotropies (IPMA) improved MTJ device, in accordance with embodiments of the present technology, is shown. The IMPA improved MTJ 400 can include one or more seed layers 405 disposed on a substrate 410. The one or more seed layers 405 can be deposited on the substrate 410 to initiate a predetermined crystalline growth in one or more subsequent deposited layers. In one implementation, the one or more seed layers 405 can include one or more layers of Tantalum (Ta), Tantalum Nitride (TaN), Chromium (Cr), Copper (Cu), Copper Nitride (CuN), Nickel (Ni), Iron (Fe), or alloys thereof with a thickness of approximately ?? nanometers (nm).


In one aspect, a Synthetic Antiferromagnetic (SAF) formation 415-425 can be disposed on the one or more seed layers 405. In one implementation, the SAF formation 415-425 can include a first ferromagnetic layer 415 disposed on the one or more seed layers 405, a first non-magnetic layer 420 disposed on the first ferromagnetic layer 415, and a second ferromagnetic layer 425 disposed on the first non-magnetic layer 420. The first ferromagnetic layer 415 can be a Cobalt (Co), Cobalt Nickel (CoNi), or Cobalt Platinum (CoPt) alloy with a thickness of approximately 1-5 nm, the first non-magnetic layer 420 can be a Ruthenium (Ru) metal with a thickness of approximately 0.90 nm, the second ferromagnetic layer 425 can be a Cobalt (Co), Cobalt Nickel (CoNi), Cobalt Platinum (CoPt) and/or Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 1-5 nm.


In one aspect, a MTJ formation 425-435 can be disposed on the SAF formation 415-425. In one aspect, the MTJ formation 425-435 can share one or more layers in common with the SAF formation 415-425. In one implementation, the MTJ formation 425-435 can include a reference magnetic layer 425, a non-magnetic tunneling barrier layer 430, and a free magnetic layer 435. The reference magnetic layer 425 and the second ferromagnetic layer 425 can be the same layer of Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 2.3 nm. For ease of explanation, where the second ferromagnetic layer 425 and the reference magnetic layer 425 are the same layer, the combined layer will be referred to as the reference magnetic layer 425. The non-magnetic tunneling barrier layer 430 can be a magnesium (Mg) oxide of approximately 1-100 nm, and the free magnetic layer 435 can be a Cobalt-Iron-Boron (Co—Fe—B) alloy with a thickness of approximately 2.3 nm. The reference magnetic layer 425 can have its magnetization pinned in a predetermined direction, meaning that the reference magnetic layer 425 has a higher coercivity than other layers and a larger magnetic field or spin-polarized current is needed to change the orientation of its magnetization. The magnetization direction of the free magnetic layer 435 can be changed by a smaller magnetic field or sin-polarized current relative to the reference magnetic layer 425.


In one aspect, the magnetization vector of the first ferromagnetic layer 415 and the reference magnetic layer 425 can be substantially perpendicular (e.g., within several degrees) to a plane of the layers (e.g., along a z-axis). The magnetization vector of the free magnetic layer 435 can also be substantially perpendicular to the plane of the layer (e.g., along a z-axis), but its direction can vary by 180 degrees.


In one aspect, an IMPA enhancement layer 455 can be disposed on the MTJ formation 425-435. The PMA enhancement layer 240 can be configured to control perpendicular magnetic anisotropy and free layer magnetization. In one aspect, one or more capping layers 460, 465 can be disposed on the IMPA enhancement layer 455. In one implementation, the one or more capping layer 460, 465 can include non-magnetic materials such as ruthenium (Ru) and tantalum (Ta). In one embodiment, the one or more capping layers 460, 465 can include a first capping layer 460 disposed on the IMPA enhancement layer 455, and a second capping layer 465 disposed on the first capping layer 460. In one implementation the first capping layer 455 can be Ruthenium (Ru) with a thickness of approximately 2-3 nm, and the second capping layer 465 can be Tantalum (a) with a thickness of approximately 3 nm.


Referring now to FIGS. 5A-5C, a block diagram illustrating fabrication of an IMPA improved MTJ device, in accordance with embodiments of the present technology, is shown. The processes of forming the seed layer 405 on the substrate 410, the SAF formation 415-425 on the seed layer 405, and the MTJ formation 425-435 on the SAF formation 415-425 are well known in the art and are not germane to understanding embodiments of the present technology, and therefore will not be described in further detail herein.


Fabrication of the IMPA improved MTJ after deposition of the MTJ formation 425-435 can continue with deposition of one or more intermediate capping layers 440, 445. In one aspect, a first intermediate capping layer 440 of Ruthenium (Ru) can be deposited on the MTJ formation 425-435, and a second intermediate capping layer 445 of Tantalum (Ta) can be deposited on the first intermediate capping layer 440. In one implementation, the Ruthenium (Ru) can be deposited using a sputtering, vapor deposition, or similar process. The Ruthenium (Ru) can be deposited to a thickness of approximately 2-5 nm. The Tantalum (Ta) can be deposited using a sputtering, vapor deposition, or similar process. The Tantalum (Ta) can be deposited to a thickness of approximately 3 nm.


In one aspect, the IPMA improved MTJ can be subject to a two-stage etching process 450 after deposition of the one or more intermediate capping layers 440, 445. The two-stage etching process 450 can include a first etch used to remove at least a portion of the one or more intermediate capping layers 440, 445. A second etch can be used to optionally remove another portion of the one or more intermediate capping layer 440, 445 and optionally remove a portion of the free magnetic layer 435 at a second rate. In one implementation, the etching process is performed until the Ruthenium (Ru) of the first intermediate capping layer 440 is substantially removed. The second etching rate can be slower than the first etching rate and used to remove any remaining Ruthenium (Ru) of the first intermediate capping layer 440. In one implementation, the slower second etching rate can also smooth the surface of the fee magnetic layer 435 as compared to the surface of the free magnetic layer 435 as deposited. Smoothing the surface of the free magnetic layer 435 can improve Interface Perpendicular Magnetic Anisotropies (IPMA) of the free magnetic layer 435. The two-stage etching process 450 can also allows for deposition of additional enhancement layers on top of the free magnetic layer 435 to control perpendicular anisotropy and free layer magnetization.


In one aspect, a PMA enhancement layer 455 includes one or more of Cobalt (Co), Iron (Fe), Boron (B) and/or Tantalum Nitride (TaN) can be deposited on the free magnetic layer 435 after the two-stage etching process 450. In one implementation, the Tantalum Nitride (TaN) can be deposited using a sputtering, vapor deposition, or similar process. The Tantalum Nitride (TaN) can be deposited to a thickness of approximately 2.0 nm. In one aspect, one or more capping layers 460, 465 can be deposited on the IPMA enhancement layer 455. In one instance, a first capping layer of Ruthenium (Ru) can be deposited on the MTJ formation 425-535, and a second capping layer 465 of Tantalum (Ta) can be deposited on the first capping layer 460. In one implementation, the Ruthenium (Ru) can be deposited using a sputtering, vapor deposition, or similar process. The Ruthenium (Ru) can be deposited to a thickness of approximately 2-5 nm. The Tantalum (Ta) can be deposited using a sputtering, vapor deposition, or similar process. The Tantalum (Ta) can be deposited to a thickness of approximately 3 nm.


In one aspect, the two-stage etching process 450, the IPMA enhancement layer 455 deposition, and the one or more capping layer 460, 465 depositions can be performed in-situ without breaking a vacuum of the fabrication equipment used to perform the etching and deposition processes. In aspect, the IPMA improved MTJ fabricated with the one or more intermediate capping layers 440, 445 can be exposed to an ambient environment for transferring to an annealing process. In one aspect, a high temperature annealing process can be configured to enhance performance of the MTJ formation 425-435. In one implementation, a high temperature annealing process can be performed after deposition of the one or more intermediate capping layers 440, 445. The one or more intermediate capping layers 440, 445 can protect the MTJ formation 425-435 from the ambient prior to, during and after annealing. By being able to perform the high temperature annealing after deposition of the one or more intermediate capping layers 440, 445, other materials that may be adversely affected by a high-temperature anneal can be utilized in the PMA enhancement layer 455, and the one or more capping layers 460, 465. In another implementation, the high temperature annealing process can be performed after deposition of the IPMA enhancement layer 455 and the one or more capping layer 460, 465. In one aspect, the two-step etching process 450, the PMA enhancement layer 455 and the one or more capping layer 460, 465 may not be sensitive to changes due to high temperature annealing. In such case, the high-temperature annealing process utilized for the SAF formation 415-425 and/or MTJ formation 425-435 can be performed after the PMA enhancement layer 455 and the one or more capping layers 460, 465 are deposited. If, however, the materials of the PMA enhancement layer 455 and/or the one or more capping layer 460, 465 are sensitive to changes due to high temperature annealing, the annealing can be performed after deposition of the one or more intermediary capping layers 440, 445.


In one implementation, the one or more seed layers 405, the SAF formation 415-425, the MTJ formation 425-435, and the first and second intermediate capping layers 440, 445 can be manufactured by a first entity. Thereafter, the partially fabricated IMPA improved MTJ device can exposed to an ambient environment for transferring to an annealing process. Fabrication can then proceed with in-situ etching to remove the first and second intermediate capping layers 440, 445, smoothing the free magnetic layer 435, and forming the optional PMA enhancement layer 455, and forming the first and second capping layers 460, 465. In another implementation, the partially fabricated IMPA improved MTJ device can exposed to an ambient environment for transferring to a second entity. The second entity can thereafter, proceed with in-situ etching to remove the first and second intermediate capping layers 440, 445, smoothing the free magnetic layer 435, and forming the optional PMA enhancement layer 455 and first and second capping layers 460, 465. Furthermore, an annealing process can be performed by either entity after formation of the first and second intermediate capping layers 440, 445.


Referring now to FIG. 6, a block diagram of a Magnetoresistive Random Access Memory (MRAM), in accordance with embodiments of the present technology, is shown. The MRAM 600 can include a memory cell array 610, an address decoder circuit 620, a word line driver circuit 630, a bit line and source line driver circuit 640, a sense circuit 650, and control circuit 660. The MRAM 600 can include other well-known circuits that are not necessary for an understanding of the present technology and therefore are not discussed herein.


The memory cell array 610 can include a plurality of memory cells organized in rows and columns, with sets of word lines, source lines and bit lines spanning the array of cells throughout the chip. In one embodiment, the memory cells can be PSC MTJ cells as described above with reference to FIGS. 2 and 3A-3C. In another embodiment, the memory cells can be IPMA improved MTJ cells as described above with reference to FIGS. 4 and 5A-5C. The address decoder 620 can map a given memory address to a particular row of MTJ memory cells in the array. The output of the address decoder 620 can be input to the word line driver 630. The output of the word line driver 630 can drive the word lines to select a given word line of the array. The bit line and source line driver 640 and the sense circuit 650 utilize the source lines and bit lines of the array to read from and write to memory cells of a selected word line of the array.


In one aspect, the control circuit 660 can be configured to cause the bit line and source line driver circuit 640 to apply appropriate write voltages to bit lines, source lines and word lines to write data to cells in a selected word. The magnetic polarity, and corresponding logic state, of the free layer of the MTJ can be changed to one of two states depending upon the direction of current flowing through the MTJ. For read operations, the control circuit 660 can be configured to cause the bit line and source line driver circuit 640 to apply appropriate read voltages to the bit lines, sources lines and word lines to cause a current to flow in the source lines that can be sensed by the sense circuit 650 to read data from cells in a selected word.


Referring now to FIG. 7, a circuit diagram of a MRAM memory cell array, in accordance with the conventional art, is shown. Again, the memory cell array 700 can include a plurality of MTJ memory cells 705, a plurality of word lines 710-720, a plurality of bit lines 725-735 and a plurality of source lines 740-750. The word lines 710-720 of the memory cell array 700 can be organized along columns of the array. The bit lines 725-735 and source lines 740-750 can be organized along rows of the array. Each memory cell 705 can comprise a MTJ cell and an access transistor. The gates of the access transistors arranged along columns of the array can be coupled to respective word lines 710-720. The sources of the access transistors arranged along rows of the array can be coupled to respective source lines 740-750. The free magnetic layer of the MTJ cells arranged along rows of the array can be coupled to a respective bit line 725-735.


In one example, to read data from a given MTJ cell 705, the respective bit line BL(m) 730 can be biased at a bit line read potential (e.g., VBLR) and the respective source line SL(m) 745 can be biased at ground (e.g., 0). When the respective word line WL(n) 715 is biased at a word line read voltage potential (e.g., VWLR) a current proportional to the resistance of the MTJ of the cell 705 will flow from the respective bit line BL(m) 730 to the respective source line SL(m) 745. In such case, the current sensed on the respective bit line BL(m) 730 can indicate the state of the selected cell 705.


To write a logic ‘0’ state to the given memory cell 705, the respective bit line BL(m) 730 can be biased at a bit line write potential (e.g., VBLW) and the respective source line SL(m) 745 can be biased at ground (e.g., 0). When the respective word line WL(n) 715 is biased at a word line write potential (e.g., VWLW) a resulting current flowing through the MTJ of the cell 705 in a first direction will cause the free magnetic layer into a state corresponding to a logic ‘0’ state. To write a logic ‘1’ state to the given memory cell 705, the respective bit line BL(m) 730 can be biased at ground (e.g., 0) and the respective source line SL(m) 745 can be biased at a source line write potential (e.g., VSLW). When the respective word line WL(n) 715 is biased at a word line write potential (e.g., VWLW) a resulting current flowing through the MTJ of the cell 705 in a second direction will cause the free magnetic layer into a state corresponding to a logic ‘1’ state.


In another example, to read data from a given memory cell 705, the respective bit line BL(m) 730 can be biased at ground (e.g., 0) and the respective source line SL(m) 745 can be biased at a bit line read potential (e.g., VBLR). When the respective word line WL(n) 715 is biased at a word line read potential (e.g., VWRL) a current proportional to the resistance of the MTJ of the given cell 705 will flow. In such case, the current sensed on the respective source line SL(m) 745 can indicate the state of the selected cell 705.


To write a logic ‘0’ state to the given memory cell 705, the respective bit line BL(m) 730 can be biased at a bit line write potential (e.g., VBLW) and the respective source line SL(m) 745 can be biased at ground (e.g., 0). When the respective word line WL(n) 715 is biased at a word line write potential (e.g., VWLW) a resulting current flowing through the MTJ of the cell 705 in a first direction will cause the free magnetic layer into a logic ‘0’ state. To write a logic ‘1’ state to a given memory cell 705, the respective bit line BL(m) 730 can be biased at ground (e.g., 0) and the respective source line SL(m) 745 can be biased at a source line write potential (e.g., VSLW). When the respective word line WL(n) 715 is biased at a word line write state (e.g., VWLW) a resulting current flowing through the MTJ of the cell 705 in a second direction will cause the free magnetic layer into a logic ‘1’ state.


The foregoing descriptions of specific embodiments of the present technology have been presented for purposes of illustration and description. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed, and obviously many modifications and variations are possible in light of the above teaching. The embodiments were chosen and described in order to best explain the principles of the present technology and its practical application, to thereby enable others skilled in the art to best utilize the present technology and various embodiments with various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the claims appended hereto and their equivalents.

Claims
  • 1. A method of fabricating a Magnetic Tunnel Junction (MTJ) device comprising: depositing a first Precessional Spin Current (PSC) magnetic layer on a MTJ formation, wherein the first PSC magnetic layer includes Iron (Fe);depositing a second PSC magnetic layer on the first PSC magnetic layer, wherein the second PSC magnetic layer includes Ruthenium (Ru);etching at least a portion of the second PSC magnetic layer with a first etch process to smooth the surface of the Ruthenium (Ru) of the second PSC magnetic layer as deposited;depositing a third PSC magnetic layer on the second PSC magnetic layer after the first etch of the second PSC magnetic layer, wherein the third PSC magnetic layer includes one or more of Cobalt (Co), Iron (Fe) and Boron (B); anddepositing a capping layer on the third magnetic layer.
  • 2. The method of fabricating the MTJ device according to claim 1, wherein: the first PSC magnetic layer has a deposited thickness of approximately 0.4-1.0 nanometers (nm);the second PSC magnetic layer has a deposited thickness of approximately 0.5-3.0 nm after the first etch of the second PSC magnetic layer; andthe third PSC magnetic layer has a deposited thickness of approximately 1-5 nm.
  • 3. The method of fabricating the MTJ device according to claim 1, wherein: the first and second PSC magnetic layers are deposited in a first vacuum instance; andthe second PSC magnetic layer is etched and the third PSC magnetic layer and the capping layer are deposited in a second vacuum instance.
  • 4. The method of fabricating the MTJ device according to claim 3, further comprising: annealing the MTJ formation after depositing the first and second PSC magnetic layers and before etching the second PSC magnetic layer.
  • 5. The method of fabricating the MTJ device according to claim 4, further comprising: depositing an intermediate capping layer on the second PSC magnetic layer in the first vacuum instance; andetching the intermediate capping layer with a second etch in the second vacuum instance, wherein the second etch and the first etch comprise a two-step etching process where the second etch is faster than the first etch.
  • 6. The method of fabricating the MTJ device according to claim 3, further comprising: depositing a PSC coupling layer in the first vacuum instance, wherein the PSC coupling layer is disposed between the first PSC magnetic layer and the MTJ formation.
  • 7. The method of fabricating the MTJ device according to claim 3, further comprising: depositing a Perpendicular Magnetic Anisotropy (PMA) enhancement layer in the first vacuum instance, wherein the PMA enhancement layer is disposed between the first PSC magnetic layer and the MTJ formation.
  • 8. The method of fabricating the MTJ device according to claim 6, further comprising: depositing a reference magnetic layer of the MTJ formation in the first vacuum instance, wherein the reference magnetic layer is disposed on a substrate;depositing a non-magnetic tunneling barrier layer of the MTJ formation in the first vacuum instance, wherein the non-magnetic tunneling barrier layer is disposed on the reference magnetic layer; anddepositing a free magnetic layer of the MTJ formation in the first vacuum instance, wherein the free magnetic layer is disposed on the non-magnetic tunneling barrier layer.
  • 9. The method of fabricating the MTJ device according to claim 8, wherein: the reference magnetic layer includes one or more of Cobalt (Co), Iron (Fe), Boron (B), Cobalt Nickel (CoNi), Cobalt Platinum (CoPt), and has a deposited thickness of approximately 1-5 nanometers (nm);the non-magnetic tunneling barrier layer includes Magnesium (Mg) oxide, and has a deposited thickness of approximately 1-10 nm; andthe free magnetic layer includes one or more of Cobalt (Co), Iron (Fe) and Boron (B), and has a deposited thickness of approximately 1-3 nm.
  • 10. The method of fabricating the MTJ device according to claim 8, further comprising: depositing a first ferromagnetic layer of a Synthetic Antiferromagnetic (SAF) formation in the first vacuum instance, wherein the first ferromagnetic layer is disposed on the substrate; anddepositing a first non-magnetic layer of the SAF formation in the first vacuum instance, wherein the first non-magnetic layer is disposed between the first ferromagnetic layer and the reference magnetic layer.
  • 11. The method of fabricating the MTJ device according to claim 10, wherein the first ferromagnetic layer includes one or more of Cobalt (Co), Cobalt Nickel (CoNi) and Cobalt Platinum (CoPt), and has a deposited thickness of approximately 1-5 nm; andthe first non-magnetic layer includes Ruthenium (Ru), and has a deposited thickness of approximately 0.9 nm.
  • 12. The method of fabricating the MTJ device according to claim 11, further comprising: depositing a seed layer in the first vacuum instance, wherein the seed layer is disposed between the substrate and the first ferromagnetic layer.
  • 13. The method of fabricating the MTJ device according to claim 1, wherein the MTJ device comprises a Magnetoresistive Random Access Memory (MRAM).
  • 14. A method of fabricating a Magnetic Tunnel Junction (MTJ) device comprising: receiving a wafer including a first Precessional Spin Current (PSC) magnetic layer disposed on a MTJ formation and a second PSC magnetic layer disposed on the first PSC magnetic, wherein the first PSC magnetic layer includes Iron (Fe) and the second PSC magnetic layer includes Ruthenium (Ru);etching at least a first portion of the second PSC magnetic layer with a first etch process to remove the first portion of the second PSC magnetic layer;etching at least a second portion of the second PSC magnetic layer with a second etch process to smooth the surface of the Ruthenium (Ru) of the second PSC magnetic layer as deposited, wherein the second etch process is slower than the first etch process;depositing a third PSC magnetic layer on the second PSC magnetic layer after the second etch of the second PSC magnetic layer, wherein the third PSC magnetic layer includes one or more of Cobalt (Co), Iron (Fe) and Boron (B); anddepositing a capping layer on the third magnetic layer.
  • 15. The method of fabricating the MTJ device according to claim 14, further comprising: annealing the wafer before etching at least the first portion of the second PSC magnetic layer.
  • 16. The method of fabricating the MTJ device according to claim 14, wherein: the first PSC magnetic layer has a deposited thickness of approximately 0.4-1.0 nanometers (nm);the second PSC magnetic layer has a deposited thickness of approximately 0.5-3.0 nm after the second etch of the second PSC magnetic layer; andthe third PSC magnetic layer has a deposited thickness of approximately 1-5 nm.
US Referenced Citations (443)
Number Name Date Kind
4597487 Crosby et al. Jul 1986 A
5541868 Prinz Jul 1996 A
5559952 Fujimoto Sep 1996 A
5629549 Johnson May 1997 A
5640343 Gallagher et al. Jun 1997 A
5654566 Johnson Aug 1997 A
5691936 Sakakima et al. Nov 1997 A
5695846 Lange et al. Dec 1997 A
5695864 Zlonczewski Dec 1997 A
5732016 Chen et al. Mar 1998 A
5751647 O'Toole May 1998 A
5856397 Mauri Jan 1999 A
5856897 Mauri Jan 1999 A
5896252 Kanai Apr 1999 A
5966323 Chen et al. Oct 1999 A
6016269 Peterson et al. Jan 2000 A
6055179 Koganei et al. Apr 2000 A
6064948 West May 2000 A
6075941 Itoh Jun 2000 A
6097579 Gill Aug 2000 A
6112295 Bhamidipati et al. Aug 2000 A
6124711 Tanaka et al. Sep 2000 A
6134138 Lu et al. Oct 2000 A
6140838 Johnson Oct 2000 A
6154139 Kanai et al. Nov 2000 A
6154349 Kanai et al. Nov 2000 A
6172902 Wegrowe et al. Jan 2001 B1
6233172 Chen et al. May 2001 B1
6233690 Choi et al. May 2001 B1
6243288 Ishikawa et al. Jun 2001 B1
6252798 Satoh et al. Jun 2001 B1
6256223 Sun Jul 2001 B1
6292389 Chen et al. Sep 2001 B1
6347049 Childress et al. Feb 2002 B1
6376260 Chen et al. Apr 2002 B1
6385082 Abraham et al. May 2002 B1
6436526 Odagawa et al. Aug 2002 B1
6442681 Ryan et al. Aug 2002 B1
6458603 Kersch et al. Oct 2002 B1
6493197 Ito et al. Dec 2002 B2
6522137 Sun et al. Feb 2003 B1
6532164 Redon et al. Mar 2003 B2
6538918 Swanson et al. Mar 2003 B2
6545903 Savtchenko et al. Apr 2003 B1
6545906 Savtchenko et al. Apr 2003 B1
6563681 Sasaki et al. May 2003 B1
6566246 deFelipe et al. May 2003 B1
6603677 Redon et al. Aug 2003 B2
6653153 Doan et al. Nov 2003 B2
6654278 Engel et al. Nov 2003 B1
6677165 Lu et al. Jan 2004 B1
6710984 Yuasa et al. Mar 2004 B1
6713195 Wang et al. Mar 2004 B2
6714444 Huai et al. Mar 2004 B2
6731537 Kanamori May 2004 B2
6744086 Daughton et al. Jun 2004 B2
6750491 Sharma et al. Jun 2004 B2
6765824 Kishi et al. Jul 2004 B2
6772036 Eryurek et al. Aug 2004 B2
6773515 Li et al. Aug 2004 B2
6777730 Daughton et al. Aug 2004 B2
6785159 Tuttle Aug 2004 B2
6812437 Levy Nov 2004 B2
6829161 Huai et al. Dec 2004 B2
6835423 Chen et al. Dec 2004 B2
6838740 Huai et al. Jan 2005 B2
6839821 Estakhri Jan 2005 B2
6842317 Sugita et al. Jan 2005 B2
6847547 Albert et al. Jan 2005 B2
6887719 Lu et al. May 2005 B2
6888742 Nguyen et al. May 2005 B1
6902807 Argoitia et al. Jun 2005 B1
6906369 Ross et al. Jun 2005 B2
6920063 Huai et al. Jul 2005 B2
6933155 Albert et al. Aug 2005 B2
6938142 Pawlowski Aug 2005 B2
6958927 Nguyen et al. Oct 2005 B1
6967863 Huai Nov 2005 B2
6980469 Kent et al. Dec 2005 B2
6985385 Nguyen et al. Jan 2006 B2
6992359 Nguyen et al. Jan 2006 B2
6995962 Saito et al. Feb 2006 B2
7002839 Kawabata et al. Feb 2006 B2
7005958 Wan Feb 2006 B2
7006371 Matsuoka Feb 2006 B2
7006375 Covington Feb 2006 B2
7009377 Huai et al. Mar 2006 B2
7009877 Huai et al. Mar 2006 B1
7041598 Sharma May 2006 B2
7045368 Hong et al. May 2006 B2
7057922 Fukumoto Jun 2006 B2
7170778 Kent et al. Jan 2007 B2
7187577 Wang Mar 2007 B1
7190611 Nguyen et al. Mar 2007 B2
7203129 Lin et al. Apr 2007 B2
7227773 Nguyen et al. Jun 2007 B1
7262941 Li et al. Aug 2007 B2
7307876 Kent et al. Dec 2007 B2
7324387 Bergemont et al. Jan 2008 B1
7335960 Han et al. Feb 2008 B2
7351594 Bae et al. Apr 2008 B2
7352021 Bae et al. Apr 2008 B2
7372722 Jeong May 2008 B2
7376006 Bednorz et al. May 2008 B2
7386765 Ellis Jun 2008 B2
7436699 Tanizaki Oct 2008 B2
7449345 Horng et al. Nov 2008 B2
7453719 Sakimura Nov 2008 B2
7476919 Hong et al. Jan 2009 B2
7502249 Ding Mar 2009 B1
7573737 Kent et al. Aug 2009 B2
7598555 Papworth-Parkin Oct 2009 B1
7619431 DeWilde et al. Nov 2009 B2
7642612 Izumi et al. Jan 2010 B2
7660161 Van Tran Feb 2010 B2
7733699 Roohparvar Jun 2010 B2
7773439 Do et al. Aug 2010 B2
7776665 Izumi et al. Aug 2010 B2
7852662 Yang Dec 2010 B2
7881095 Lu Feb 2011 B2
7911832 Kent et al. Mar 2011 B2
7936595 Han et al. May 2011 B2
7986544 Kent et al. Jul 2011 B2
8080365 Nozaki Dec 2011 B2
8088556 Nozaki Jan 2012 B2
8094480 Tonomura Jan 2012 B2
8144509 Jung Mar 2012 B2
8148970 Fuse Apr 2012 B2
8255742 Ipek Aug 2012 B2
8278996 Miki Oct 2012 B2
8279666 Dieny et al. Oct 2012 B2
8334213 Mao Dec 2012 B2
8349536 Nozaki Jan 2013 B2
8363465 Kent et al. Jan 2013 B2
8386836 Burger Feb 2013 B2
8432727 Ryu Apr 2013 B2
8441844 El Baraji May 2013 B2
8456883 Liu Jun 2013 B1
8456926 Ong Jun 2013 B2
8492881 Kuroiwa et al. Jul 2013 B2
8535952 Ranjan et al. Sep 2013 B2
8539303 Lu Sep 2013 B2
8549303 Fifield et al. Oct 2013 B2
8574928 Satoh et al. Nov 2013 B2
8582353 Lee Nov 2013 B2
8593868 Park Nov 2013 B2
8617408 Balamane Dec 2013 B2
8625339 Ong Jan 2014 B2
8634232 Oh Jan 2014 B2
8716817 Saida May 2014 B2
8737137 Choy et al. May 2014 B1
8780617 Kang Jul 2014 B2
8792269 Abedifard Jul 2014 B1
8852760 Wang et al. Oct 2014 B2
8902628 Ha Dec 2014 B2
8966345 Wilkerson Feb 2015 B2
9019754 Bedeschi Apr 2015 B1
9026888 Kwok May 2015 B2
9043674 Wu May 2015 B2
9082888 Kent et al. Jul 2015 B2
9104595 Sah Aug 2015 B2
9140747 Kim Sep 2015 B2
9165629 Chih Oct 2015 B2
9166155 Deshpande Oct 2015 B2
9229853 Khan Jan 2016 B2
9245608 Chen et al. Jan 2016 B2
9250990 Motwani Feb 2016 B2
9263667 Pinarbasi Feb 2016 B1
9298552 Leem Mar 2016 B2
9299412 Naeimi Mar 2016 B2
9317429 Ramanujan Apr 2016 B2
9337412 Pinarbasi et al. May 2016 B2
9362486 Kim et al. Jun 2016 B2
9378317 Kawai Jun 2016 B2
9396991 Arvin et al. Jul 2016 B2
9401336 Arvin et al. Jul 2016 B2
9406876 Pinarbasi Aug 2016 B2
9418721 Bose Aug 2016 B2
9449720 Lung Sep 2016 B1
9450180 Annunziata Sep 2016 B1
9455013 Kim Sep 2016 B2
9472282 Lee Oct 2016 B2
9472748 Kuo et al. Oct 2016 B2
9484527 Han et al. Nov 2016 B2
9488416 Fujita et al. Nov 2016 B2
9508456 Shim Nov 2016 B1
9548445 Lee et al. Jan 2017 B2
9553102 Wang Jan 2017 B2
9583167 Chung Feb 2017 B2
9728712 Kardasz et al. Aug 2017 B2
9741926 Pinarbasi et al. Aug 2017 B1
9772555 Park et al. Sep 2017 B2
9773974 Pinarbasi et al. Sep 2017 B2
9853006 Avin et al. Dec 2017 B2
9853206 Pinarbasi et al. Dec 2017 B2
9853292 Loveridge et al. Dec 2017 B2
9865806 Choi et al. Jan 2018 B2
10026609 Sreenivasan et al. Jul 2018 B2
10043851 Shen Aug 2018 B1
10115446 Louie et al. Oct 2018 B1
10163479 Yoha Dec 2018 B2
20020057593 Hidaka May 2002 A1
20020090533 Zhang et al. Jul 2002 A1
20020105823 Redon et al. Aug 2002 A1
20020132140 Igarashi et al. Sep 2002 A1
20030085186 Fujioka May 2003 A1
20030117840 Sharma et al. Jun 2003 A1
20030151944 Saito Aug 2003 A1
20030197984 Inomata et al. Oct 2003 A1
20030218903 Luo Nov 2003 A1
20040012994 Slaughter et al. Jan 2004 A1
20040026369 Ying Feb 2004 A1
20040047179 Chan Mar 2004 A1
20040061154 Huai et al. Apr 2004 A1
20040094785 Zhu et al. May 2004 A1
20040130936 Nguyen et al. Jul 2004 A1
20040173315 Leung Sep 2004 A1
20040197174 Van Den Berg Oct 2004 A1
20040221030 Huras Nov 2004 A1
20040257717 Sharma et al. Dec 2004 A1
20050022746 Lampe Feb 2005 A1
20050029551 Atwood et al. Feb 2005 A1
20050041342 Huai et al. Feb 2005 A1
20050051820 Stojakovic et al. Mar 2005 A1
20050063222 Huai et al. Mar 2005 A1
20050104101 Sun et al. May 2005 A1
20050128842 Wei Jun 2005 A1
20050136600 Huai Jun 2005 A1
20050158881 Sharma Jul 2005 A1
20050160205 Kuo Jul 2005 A1
20050174702 Gill Aug 2005 A1
20050180202 Huai et al. Aug 2005 A1
20050184839 Nguyen et al. Aug 2005 A1
20050201023 Huai et al. Sep 2005 A1
20050237787 Huai et al. Oct 2005 A1
20050251628 Jarvis et al. Nov 2005 A1
20050280058 Pakala et al. Dec 2005 A1
20050285176 Kim Dec 2005 A1
20060018057 Huai Jan 2006 A1
20060049472 Diao et al. Mar 2006 A1
20060077734 Fong Apr 2006 A1
20060087880 Mancoff et al. Apr 2006 A1
20060092696 Bessho May 2006 A1
20060132990 Morise et al. Jun 2006 A1
20060198202 Erez Sep 2006 A1
20060227465 Inokuchi et al. Oct 2006 A1
20060271755 Miura Nov 2006 A1
20060284183 Izumi et al. Dec 2006 A1
20060291305 Suzuki et al. Dec 2006 A1
20070019337 Apalkov et al. Jan 2007 A1
20070094573 Chen Apr 2007 A1
20070096229 Yoshikawa May 2007 A1
20070220935 Cernea Sep 2007 A1
20070226592 Radke Sep 2007 A1
20070242501 Hung et al. Oct 2007 A1
20070283313 Ogawa Dec 2007 A1
20070285972 Horii Dec 2007 A1
20080049487 Yoshimura Feb 2008 A1
20080049488 Rizzo Feb 2008 A1
20080079530 Weidman et al. Apr 2008 A1
20080112094 Kent et al. May 2008 A1
20080144376 Lee Jun 2008 A1
20080151614 Guo Jun 2008 A1
20080181009 Arai Jul 2008 A1
20080259508 Kent et al. Oct 2008 A2
20080294938 Kondo Nov 2008 A1
20080297292 Viala et al. Dec 2008 A1
20090040825 Adusumilli et al. Feb 2009 A1
20090046501 Ranjan et al. Feb 2009 A1
20090072185 Raksha et al. Mar 2009 A1
20090078927 Xiao Mar 2009 A1
20090080267 Bedeschi Mar 2009 A1
20090091037 Assefa et al. Apr 2009 A1
20090098413 Kanegae Apr 2009 A1
20090130779 Li May 2009 A1
20090146231 Kuper et al. Jun 2009 A1
20090161421 Cho et al. Jun 2009 A1
20090209102 Zhong et al. Aug 2009 A1
20090231909 Dieny et al. Sep 2009 A1
20100039136 Chua-Eoan Feb 2010 A1
20100080040 Choi Apr 2010 A1
20100087048 Izumi et al. Apr 2010 A1
20100110803 Arai May 2010 A1
20100124091 Cowburn May 2010 A1
20100162065 Norman Jun 2010 A1
20100193891 Wang et al. Aug 2010 A1
20100195362 Norman Aug 2010 A1
20100195401 Jeong et al. Aug 2010 A1
20100227275 Nozaki Sep 2010 A1
20100232206 Li Sep 2010 A1
20100246254 Prejbeanu et al. Sep 2010 A1
20100248154 Nozaki Sep 2010 A1
20100254181 Chung Oct 2010 A1
20100271090 Rasmussen Oct 2010 A1
20100271870 Zheng et al. Oct 2010 A1
20100277976 Oh Nov 2010 A1
20100290275 Park Nov 2010 A1
20100311243 Mao Dec 2010 A1
20110001108 Greene Jan 2011 A1
20110032645 Noel et al. Feb 2011 A1
20110058412 Zheng et al. Mar 2011 A1
20110061786 Mason Mar 2011 A1
20110076620 Nozaki Mar 2011 A1
20110089511 Keshtbod et al. Apr 2011 A1
20110133298 Chen et al. Jun 2011 A1
20110283135 Burger Nov 2011 A1
20110310691 Zhou et al. Dec 2011 A1
20110320696 Fee et al. Dec 2011 A1
20120028373 Belen Feb 2012 A1
20120052258 Op DeBeeck et al. Mar 2012 A1
20120069649 Ranjan et al. Mar 2012 A1
20120127804 Ong et al. May 2012 A1
20120155158 Higo Jun 2012 A1
20120163113 Hatano et al. Jun 2012 A1
20120280336 Watts Jun 2012 A1
20120181642 Prejbeanu et al. Jul 2012 A1
20120188818 Ranjan et al. Jul 2012 A1
20120221905 Burger Aug 2012 A1
20120228728 Ueki et al. Sep 2012 A1
20120239969 Dickens Sep 2012 A1
20120254636 Tsukamoto et al. Oct 2012 A1
20120280339 Zhang et al. Nov 2012 A1
20120294078 Kent et al. Nov 2012 A1
20120299133 Son et al. Nov 2012 A1
20120324274 Hori Dec 2012 A1
20130001506 Sato et al. Jan 2013 A1
20130001652 Yoshikawa et al. Jan 2013 A1
20130021841 Zhou et al. Jan 2013 A1
20130039119 Rao Feb 2013 A1
20130044537 Ishigaki Feb 2013 A1
20130075845 Chen et al. Mar 2013 A1
20130107633 Kim May 2013 A1
20130244344 Malmhall Sep 2013 A1
20130267042 Satoh et al. Oct 2013 A1
20130270523 Wang et al. Oct 2013 A1
20130270661 Yi et al. Oct 2013 A1
20130275691 Chew Oct 2013 A1
20130307097 Yi et al. Nov 2013 A1
20130341801 Satoh et al. Dec 2013 A1
20140009994 Parkin et al. Jan 2014 A1
20140036573 Ishihara Feb 2014 A1
20140042571 Gan et al. Feb 2014 A1
20140048896 Huang et al. Feb 2014 A1
20140063949 Tokiwa Mar 2014 A1
20140070341 Beach et al. Mar 2014 A1
20140089762 Pangal et al. Mar 2014 A1
20140103469 Jan Apr 2014 A1
20140103472 Kent et al. Apr 2014 A1
20140136870 Breternitz et al. May 2014 A1
20140149827 Kim et al. May 2014 A1
20140151837 Ryu Jun 2014 A1
20140169085 Wang et al. Jun 2014 A1
20140177316 Otsuka et al. Jun 2014 A1
20140217531 Jan Aug 2014 A1
20140219034 Gomez et al. Aug 2014 A1
20140252439 Guo Sep 2014 A1
20140264671 Chepulskyy et al. Sep 2014 A1
20140269005 Kang Sep 2014 A1
20140281284 Block et al. Sep 2014 A1
20140289358 Lindamood Sep 2014 A1
20140321196 Ikeda Oct 2014 A1
20150056368 Wang et al. Feb 2015 A1
20150098287 Lee Apr 2015 A1
20150100848 Kalamatianos Apr 2015 A1
20150135039 Mekhanik et al. May 2015 A1
20150143343 Weiss May 2015 A1
20150154116 Dittrich Jun 2015 A1
20150171316 Park et al. Jun 2015 A1
20150206568 Bose et al. Jul 2015 A1
20150206569 Bose et al. Jul 2015 A1
20150242269 Pelley et al. Aug 2015 A1
20150262701 Takizawa Sep 2015 A1
20150278011 Keppel et al. Oct 2015 A1
20150279904 Pinarbasi et al. Oct 2015 A1
20150378814 Webb et al. Dec 2015 A1
20150380088 Naeimi et al. Dec 2015 A1
20160027525 Kim et al. Jan 2016 A1
20160027999 Pinarhasi Jan 2016 A1
20160043304 Chen Feb 2016 A1
20160056072 Arvin et al. Feb 2016 A1
20160085443 Tomishima et al. Mar 2016 A1
20160085621 Motwani Mar 2016 A1
20160086600 Bauer et al. Mar 2016 A1
20160087193 Yoha Mar 2016 A1
20160093798 Kim et al. Mar 2016 A1
20160111634 Lee et al. Apr 2016 A1
20160118249 Sreenivasan et al. Apr 2016 A1
20160124299 Yu et al. May 2016 A1
20160126201 Arvin et al. May 2016 A1
20160126452 Kuo et al. May 2016 A1
20160126453 Chen et al. May 2016 A1
20160148685 Roy May 2016 A1
20160163965 Han et al. Jun 2016 A1
20160163973 Pinarbasi Jun 2016 A1
20160181508 Lee et al. Jun 2016 A1
20160218278 Pinarbasi et al. Jul 2016 A1
20160260486 Tani Sep 2016 A1
20160268499 You Sep 2016 A1
20160283385 Boyd et al. Sep 2016 A1
20160284762 Wang et al. Sep 2016 A1
20160300615 Lee Oct 2016 A1
20160307860 Arvin et al. Oct 2016 A1
20160315118 Kardasz et al. Oct 2016 A1
20160315249 Kardasz et al. Oct 2016 A1
20160315259 Fennimore et al. Oct 2016 A1
20160085692 Kwok Dec 2016 A1
20160358778 Park et al. Dec 2016 A1
20160372656 Pinarbasi Dec 2016 A1
20160378592 Ikegami et al. Dec 2016 A1
20170025472 Kim et al. Jan 2017 A1
20170033156 Gan et al. Feb 2017 A1
20170033283 Pinarbasi et al. Feb 2017 A1
20170047107 Berger et al. Feb 2017 A1
20170062705 Yamakawa Mar 2017 A1
20170062712 Choi et al. Mar 2017 A1
20170069837 Choi et al. Mar 2017 A1
20170084826 Zhou et al. Mar 2017 A1
20170123991 Sela et al. May 2017 A1
20170133104 Darbari et al. May 2017 A1
20170199459 Ryu et al. Jul 2017 A1
20170222132 Pinarbasi et al. Aug 2017 A1
20170270988 Ikegami Sep 2017 A1
20180018134 Kang Jan 2018 A1
20180019343 Asami Jan 2018 A1
20180033957 Zhang Feb 2018 A1
20180097175 Chuang Apr 2018 A1
20180114589 El-Baraji et al. Apr 2018 A1
20180119278 Kornmeyer May 2018 A1
20180121117 Berger et al. May 2018 A1
20180121355 Berger et al. May 2018 A1
20180121361 Berger et al. May 2018 A1
20180122446 Berger et al. May 2018 A1
20180122447 Berger et al. May 2018 A1
20180122448 Berger et al. May 2018 A1
20180122449 Berger et al. May 2018 A1
20180122450 Berger et al. May 2018 A1
20180130945 Choi et al. May 2018 A1
20180211821 Kogler Jul 2018 A1
20180233362 Glodde Aug 2018 A1
20180233363 Glodde Aug 2018 A1
20180248110 Kardasz et al. Aug 2018 A1
20180248113 Pinarbasi et al. Aug 2018 A1
20180331279 Shen Nov 2018 A1
Foreign Referenced Citations (27)
Number Date Country
2766141 Jan 2011 CA
105706259 Jun 2016 CN
1345277 Sep 2003 EP
2817998 Jun 2002 FR
2832542 May 2003 FR
2910716 Jun 2008 FR
H10-004012 Jan 1998 JP
H11-120758 Apr 1999 JP
H11-352867 Dec 1999 JP
2001-195878 Jul 2001 JP
2002-261352 Sep 2002 JP
2002-357489 Dec 2002 JP
2003-318461 Nov 2003 JP
2005-044848 Feb 2005 JP
2005-150482 Jun 2005 JP
2005-535111 Nov 2005 JP
2006128579 May 2006 JP
2008-524830 Jul 2008 JP
2009-027177 Feb 2009 JP
2013-012546 Jan 2013 JP
2014-039061 Feb 2014 JP
5635666 Dec 2014 JP
2015-002352 Jan 2015 JP
10-2014-015246 Sep 2014 KR
2009-080636 Jul 2009 WO
2011-005484 Jan 2011 WO
2014-062681 Apr 2014 WO
Non-Patent Literature Citations (11)
Entry
US 7,026,672 B2, 04/2006, Grandis (withdrawn)
US 2016/0218273 A1, 06/2016, Pinarbasi (withdrawn)
Bhatti Sabpreet et al., “Spintronics Based Random Access Memory: a Review,” Material Today, Nov. 2107, pp. 530-548, vol. 20, No. 9, Elsevier.
Helia Naeimi, et al., “STTRAM Scaling and Retention Failure,” Intel Technology Journal, vol. 17, issue 1, 2013, pp. 54-75 (22 pages).
S. Ikeda, et al., “A Perpendicular-Anisotropy CoFeB—MgO Magnetic Tunnel Junction”, Nature Materials, vol. 9, Sep. 2010, pp. 721-724 (4 pages).
R.H. Kock, et al., “Thermally Assisted Magnetization Reversal in Submicron-Sized Magnetic Thin Films”, Physical Review Letters, The American Physical Society, vol. 84, No. 23, Jun. 5, 2000, pp. 5419-5422 (4 pages).
K.J. Lee, et al., “Analytical Investigation of Spin-Transfer Dynamics Using Perpendicular-to-Plane Polarizer”, Applied Physics Letters, American Insitute of Physics, vol. 86, (2005), pp, 022505-1-022505-3 (3 pages).
Kirsten Martens, et al., “Thermally Induced Magnetic Switching in Thin Ferromagnetic Annuli”, NSF grants PHY-0351964 (DLS), 2005, 11 pages.
Kristen Martens, et al., “Magnetic Reversal in Nanoscropic Ferromagnetic Rings”, NSF grants PHY-0351964 (DLS) 2006, 23 pages.
“Magnetic Technology Spintronics, Media and Interface”, Data Storage Institute, R&D Highlights, Sep. 2010, 3 pages.
Daniel Scott Matic, “A Magnetic Tunnel Junction Compact Model for STT-RAM and MeRAM”, Master Thesis University of California, Los Angeles, 2013, pp. 43.
Related Publications (1)
Number Date Country
20190207097 A1 Jul 2019 US