Abstract
Developing simple ways to control spin states in spintronic devices is a crucial step towards increasing their functionality. MnTe is a room-temperature antiferromagnet with promising spintronic properties, including for thermospintronics and magnon-based devices. Here, we show that, in MnTe, less than 1% Li is sufficient to produce a dramatic spin reorientation as observed by neutron diffraction. The behavior of the 0001 magnetic Bragg peak reveals a significant reorientation of the Mn spins from planar in the pure material to almost completely axial with minimal Li doping. Temperature dependence of the magnetic peaks in Li-doped samples indicates that axial spins shift back to planar suddenly upon approaching the Néel temperature (TN=307 K). Density functional theory calculations support the idea that a shift in the Fermi level caused by doping is responsible for switching the material between two competing magnetic ground states. These results pave the way for developing easy switching of magnetic states in functional materials such as spintronic devices and topological insulators.
Original language | English |
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Article number | 014404 |
Journal | Physical Review Materials |
Volume | 6 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2022 |
Funding
J. Zhang and D. Abernathy are acknowledged for assistance in data acquisition and B. Frandsen and D. Mandrus are acknowledged for helpful discussions. Neutron scattering work by D.H.M. and R.P.H., anisotropy calculations by R.S.F., DFT calculations by D.S.P., and magnetization measurements and sample synthesis by J.Y. and M.A.M. were supported by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES), Materials Sciences and Engineering Division. A portion of this research (Diffraction at HB-2A, conducted with K.M.T. and S.A.C., and INS at ARCS, conducted with D. L. Abernathy) used resources at the High Flux Isotope Reactor and Spallation Neutron Source, supported by DOE, BES, Scientific User Facilities Division. H.Z. acknowledges financial support by the MOST of China (Grant No. 2018YFA0702100). Samples 3 and 4–7 were synthesized by D.V. and H.Z., respectively. D.V. acknowledges funding support by the Air Force Office of Scientific Research (AFOSR) under Contract No. FA9550-19-1-0363 and the National Science Foundation (NSF) under Grant No. ECCS-1711253.
Funders | Funder number |
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National Science Foundation | ECCS-1711253 |
U.S. Department of Energy | |
Air Force Office of Scientific Research | FA9550-19-1-0363 |
Office of Science | |
Basic Energy Sciences | |
Division of Materials Sciences and Engineering | |
Ministry of Science and Technology of the People's Republic of China | 2018YFA0702100 |