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具有铁磁半金属性和拓扑狄拉克态的多铁性磷化钒单层

A multiferroic vanadium phosphide monolayer with ferromagnetic half-metallicity and topological Dirac states.

作者信息

Xuan Xiaoyu, Wu Menghao, Zhang Zhuhua, Guo Wanlin

机构信息

State Key Laboratory of Mechanics and Control of Mechanical Structures, Key Laboratory for Intelligent Nano Materials and Devices of Ministry of Education, and Institute for Frontier Science, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China.

School of Physics and Wuhan National High Magnetic Field Center, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Nanoscale Horiz. 2022 Jan 31;7(2):192-197. doi: 10.1039/d1nh00353d.

Abstract

Ferroelasticity, ferromagnetism, half-metallicity, and topological Dirac states are properties highly sought in two-dimensional (2D) materials for advanced device applications. Here, we report first-principles prediction of a dynamically and thermally stable tetragonal vanadium phosphide (t-VP) monolayer that hosts all these desirable properties. This monolayer is substantially ferromagnetic with polarized spins aligned in the in-plane direction a dpd super-exchange coupling mechanism; meanwhile, its tetragonal lattice enables an intrinsic in-plane ferroelasticity with a reversible strain of 23.4%. As a result, the ferroelasticity is strongly coupled with ferromagnetism spinorbit coupling to enable deterministic control over the magnetocrystalline anisotropy by an applied elastic strain. More interestingly, this multiferroic t-VP monolayer possesses half-metallicity with an anisotropic, topological Dirac cone residing in the majority-spin channel. We also predict a multiferroic t-CrN monolayer, whose ferromagnetism features a high Curie temperature of up to 478 K but is weakly coupled to its in-plane ferroelasticity. These results suggest a tetragonal 2D lattice as a robust atomic-scale scaffold on the basis of which fascinating electronic and magnetic properties can be rationally created by a suitable combination of chemical elements.

摘要

铁弹性、铁磁性、半金属性和拓扑狄拉克态是二维(2D)材料中先进器件应用所高度追求的特性。在此,我们报告了一种动态和热稳定的四方磷化钒(t-VP)单层的第一性原理预测,该单层具有所有这些理想特性。这种单层具有显著的铁磁性,其极化自旋在面内方向排列——一种dpd超交换耦合机制;同时,其四方晶格具有23.4%的可逆应变,从而实现了本征面内铁弹性。因此,铁弹性与铁磁性通过自旋轨道耦合强烈耦合,从而能够通过施加弹性应变来确定性地控制磁晶各向异性。更有趣的是,这种多铁性t-VP单层具有半金属性,在多数自旋通道中存在各向异性的拓扑狄拉克锥。我们还预测了一种多铁性t-CrN单层,其铁磁性具有高达478 K的居里温度,但与其面内铁弹性的耦合较弱。这些结果表明四方二维晶格是一种强大的原子尺度支架,在此基础上,通过合适的化学元素组合可以合理地创造出迷人的电子和磁性特性。

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