Issue 36, 2022

Large perpendicular magnetic anisotropy of transition metal dimers driven by polarization switching of a two-dimensional ferroelectric In2Se3 substrate

Abstract

Large perpendicular magnetic anisotropy (MA) is highly desirable for realizing atomic-scale magnetic data storage which represents the ultimate limit of the density of magnetic recording. In this work, we study the MA of transition metal dimers Co–Os, Co–Co and Os–Os adsorbed on two-dimensional ferroelectric In2Se3 (In2Se3-CoOs, In2Se3-OsCo, In2Se3-CoCo and In2Se3-OsOs) using first-principles calculations. We find that the Co–Os dimer in In2Se3-CoOs has a total magnetic anisotropy energy (MAE) of ∼40 meV. The MAE arising from the Os atom in In2Se3-CoOs is up to ∼60 meV. Such large MAE is attributed to the high spin–orbit coupling constant and the onefold coordination of the Os atom. In addition, perpendicular MA can be enhanced in In2Se3-CoOs and induced in In2Se3-OsCo, In2Se3-CoCo and In2Se3-OsOs by the ferroelectric polarization reversal of In2Se3. We demonstrate that the enlargement of exchange splitting of dxy/dx2y2 and dxz/dyz orbitals for Os atoms in In2Se3-OsOs, Co atom in In2Se3-CoOs and Os and Co atoms in In2Se3-OsCo is responsible for the increase of MAE; while, for the upper Co atom in In2Se3-CoCo and the Os atom in In2Se3-CoOs, the energy rise of the dz2 orbital owing to the change of the crystal field effect by the reversal of ferroelectric polarization results in the increase of MAE.

Graphical abstract: Large perpendicular magnetic anisotropy of transition metal dimers driven by polarization switching of a two-dimensional ferroelectric In2Se3 substrate

Supplementary files

Article information

Article type
Paper
Submitted
23 Apr 2022
Accepted
22 Aug 2022
First published
23 Aug 2022

Phys. Chem. Chem. Phys., 2022,24, 21966-21974

Large perpendicular magnetic anisotropy of transition metal dimers driven by polarization switching of a two-dimensional ferroelectric In2Se3 substrate

W. Qiao, D. Jin, W. Mi, D. Wang, S. Yan, X. Xu and T. Zhou, Phys. Chem. Chem. Phys., 2022, 24, 21966 DOI: 10.1039/D2CP01864K

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