Spin-orbit torque in Van Der Waals heterostructures of magnetic two-dimensional materials
Creators
- 1. Department of Physics & Astronomy, University of Delaware, Newark, DE 19716 (United States)
Description
The bilayer heterostructures composed of an ultrathin ferromagnetic metal (FM) and a nonmagnetic material hosting strong spin-orbit coupling (SOC) are a principal resource for spin-orbit torque (SOT) [1] and spin-to-charge conversion [2] effects in next generation spintronics. The key to understand SOT is current-driven nonequilibrium spin density [3], which generates SOT when it is noncolliner to the direction of local magnetization and can arise due to variety of microscopic mechanisms (including spin-orbit proximity effect, spin Hall effect and interfacial scattering mechanisms). The recently discovered two-dimensional (2D) magnetic materials [4] offer new avenue for highly efficient and tunable SOT in van der Waals (vdW) heterostructures composed of few monolayers of atomically thin materials. Using first-principles quantum transport calculations, which combine nonequilibrium Green functions with noncollinear density functional theory, we predict [5] that injecting unpolarized charge current parallel to the interface of bilayer-CrI3/monolayer-TaSe2 vdW heterostructure will induce SOT driven dynamics of magnetization on the first monolayer of CrI3 that is in direct contact with metallic transition metal dichalcogenide (TMD) TaSe2. By combining calculated complex angular dependence of SOT with the Landau-Lifshitz-Gilbert equation for classical dynamics of magnetization, we find that this can reverse the direction of magnetization on the first monolayer to become parallel to that of the second monolayer, thereby converting bilayer CrI3 from antiferromagnet to ferromagnet (AFM-FM) while not requiring any external magnetic field that was crucial in recent experiments [6] inducing AFM-FM transition via electric field or electrostatic doping. We explain the mechanism of such current-driven nonequilibrium phase transition by showing that first monolayer of CrI3 becomes conducting due to doping by evanescent wavefunctions injected by metallic TaSe2, while concurrently acquiring strong SOC via this proximity effect. Another vdW heterostructure exhibiting SOT is doubly proximitized graphene, which is neither magnetic nor hosts SOC in isolated form, but proximity induced magnetic moments will exhibit SOT in Cr2Ge2Te6/graphene/WS2 vdW heterostructure which can be tuned by two orders of magnitude via the gate voltage [7]. I will also illustrate fundamentals of spin-orbit proximity effect using examples of conventional ferromagnets (such as cobalt) in contact with TMDs (such as MoS2, WSe2 and metallic TaSe2) or topological insulators (such as Bi2Se3) [8].
Additional details
Identifiers
Publishing Information
- Publisher
- JINR
- Imprint Place
- Dubna (Russian Federation)
- Imprint Title
- Low-dimensional materials: theory, modeling, experiment. Book of Abstracts
- Imprint Pagination
- 86 p.
- Journal Page Range
- p. 55-56
- Report number
- INIS-XJ--004
Conference
- Title
- International conference on low-dimensional materials
- Acronym
- LDM 2021
- Dates
- 12-17 Jul 2021
- Place
- Dubna (Russian Federation)
INIS
- Country of Publication
- Joint Institute for Nuclear Research (JINR)
- Country of Input or Organization
- Joint Institute for Nuclear Research (JINR)
- INIS RN
- 53057149
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ATOMIC FORCE MICROSCOPY; CURRENTS; DENSITY FUNCTIONAL METHOD; GRAPHENE; GREEN FUNCTION; LAYERS; L-S COUPLING; MAGNETIC MATERIALS; MAGNETIZATION; SPIN; TORQUE; TWO-DIMENSIONAL SYSTEMS; VAN DER WAALS FORCES
- Descriptors DEC
- ANGULAR MOMENTUM; CALCULATION METHODS; CARBON; COUPLING; CRYSTAL LATTICES; CRYSTAL STRUCTURE; ELEMENTS; FUNCTIONS; INTERMEDIATE COUPLING; MATERIALS; MICROSCOPY; NONMETALS; PARTICLE PROPERTIES; VARIATIONAL METHODS
Optional Information
- Notes
- 8 refs.; https://wiki.physics.udel.edu/qttg