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
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.
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, an Interface Perpendicular Magnetic Anisotropies (IPMA) improved 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 free magnetic layer of the MTJ formation can have a smoothness of approximately 0.2 nm. The IPMA improved MTJ device can further include an optional PMA enhancement layer disposed on the free magnetic layer of the MTJ formation, a first capping layer disposed on the free magnetic layer or the optional PMA enhancement layer, and a second capping layer disposed on the first capping layer.
In one embodiment, a method of manufacturing the IPMA improved MTJ device can include depositing a first intermediate capping layer on the MTJ formation and a second intermediate capping layer on the first intermediate capping layer, wherein the first intermediate capping layer includes Ruthenium (Ru) and the second intermediate capping layer includes Tantalum (Ta). The first and second intermediate capping layers 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 intermediate capping layer. The first and second intermediate capping layers can be etched by a two-step etching process. In addition, at least a portion of the free magnetic layer of the MTJ formation can be subjected to a slow etch portion of the two-step etching process to smooth the surface of the free magnetic layer. An optional PMA enhancement layer can be deposited on the free magnetic layer after the slow etch of the free magnetic layer. The first capping layer can be deposited on the free magnetic layer or the optional PMA enhancement layer, and the second capping layer can be deposited on the first capping layer, wherein the first capping layer includes Ruthenium (Ru) and the second capping layer includes Tantalum (Ta). The two-step etching process and the deposition of the first and second capping layers, and the optional PMA enhancement layer if applicable, can be performed in a second vacuum condition.
In another embodiment, a method of manufacturing the IPMA improved MTJ device can include receiving a wafer including a first intermediate capping layer disposed on a MTJ formation and a second intermediate capping layer disposed on the first intermediate capping layer. The first intermediate capping layer can include Ruthenium (Ru) and the second intermediate capping layer can include Tantalum (Ta). In a two-step etching process, the second intermediate capping layer can be etched with a fast etch of a two-stage etching process. Tt least a portion of the first intermediate capping layer and a portion of a free magnetic layer of the MTJ formation can be etched with a slow etch of the two-stage etching process to smooth the surface of the free magnetic layer as deposited. A first capping layer can be deposited on the free magnetic layer of the MTJ formation after the slow etch of the free magnetic layer. A second capping layer can be deposited on the first capping layer. The first capping layer can include Ruthenium (Ru) and the second capping layer can include Tantalum (Ta).
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.
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:
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
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
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
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
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
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 layers 440, 445 and optionally remove a portion of the free magnetic layer 435 at a second rate. In one implementation, a first etching process of a two-stage etching process can be utilized to remove at least a portion of the second intermediate capping layer 445. For example, the etching process is performed until the Ruthenium (Ru) of the first intermediate capping layer 440 is substantially removed. In one implementation, a second etching process of the two-stage etching process can be utilized to remove at least a remaining portion of the first intermediate capping layer 440. The second etching process can also be continued to remove a portion of the free magnetic layer 435 to smooth the surface of the free magnetic layer 435. For example, 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. Accordingly, the two-stage etching process removes the one or more intermediate capping layers 440, 445, leaving a smoothed surface of the free magnetic layer 435, as illustrated in
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
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
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
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.
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 | Slonczewski | Dec 1997 | A |
5732016 | Chen et al. | Mar 1998 | A |
5751647 | O'Toole | May 1998 | 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 et al. | 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 |
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 |
8747680 | Deshpande | Jun 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 |
9378817 | 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 | Arvin 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 et al. | 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 |
20050276099 | Horng | Dec 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 |
20060245116 | Klostermann | Nov 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 |
20080090307 | Xiao | 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 | Sep 2009 | A1 |
20090256220 | Horng | Oct 2009 | A1 |
20100039136 | Chua-Eoan | Feb 2010 | A1 |
20100065935 | Horng | Mar 2010 | A1 |
20100080040 | Choi | Apr 2010 | A1 |
20100087048 | Izumi et al. | Apr 2010 | A1 |
20100110803 | Arai | May 2010 | A1 |
20100124091 | Cowbum | 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 et al. | Nov 2010 | A1 |
20100304504 | Shinde | Dec 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 |
20120018826 | Lee | Jan 2012 | 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 |
20140087485 | Tomioka | 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 |
20140241047 | Guo | Aug 2014 | A1 |
20140246741 | Guo | Sep 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 |
20150194315 | Ishimaru | Jul 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 |
20150364676 | Guo | Dec 2015 | A1 |
20150378814 | Webb et al. | Dec 2015 | A1 |
20150380088 | Naeimi et al. | Dec 2015 | A1 |
20160027525 | Kim et al. | Jan 2016 | A1 |
20160027999 | Pinarbasi | 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 |
20160085692 | Kwok | Mar 2016 | A1 |
20160086600 | Bauer et al. | Mar 2016 | A1 |
20160087193 | Pinarbasi et al. | 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 |
20160180929 | Kang | 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 |
20160308112 | Tan | Oct 2016 | A1 |
20160315118 | Kardasz et al. | Oct 2016 | A1 |
20160315249 | Kardasz et al. | Oct 2016 | A1 |
20160315259 | Fennimore et al. | Oct 2016 | A1 |
20160351799 | Xue | Dec 2016 | A1 |
20160358778 | Park et al. | Dec 2016 | A1 |
20160372656 | Pinarbasi et al. | 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 |
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 |
20170125668 | Paranjpe | 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 |
20180197914 | Jeong | Jul 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 |
20190067566 | Nagel | Feb 2019 | A1 |
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 |
Entry |
---|
US 7,026,672 B2, 04/2006, Grandis (withdrawn) |
Bhatti Sabpreet et al., “Spintronics Based Raridorn 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 a Perpendicular-to-Plane Polarizer”, Applied Physics Letters, American Insitute of Physics, vol. 86, (2005), pp. 022505-1 to 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-031964 (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. |
Number | Date | Country | |
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20190207095 A1 | Jul 2019 | US |