Suppr超能文献

范德华单分子层中自旋手性驱动的多铁性

Spin-Chirality-Driven Multiferroicity in van der Waals Monolayers.

作者信息

Liu Chao, Ren Wei, Picozzi Silvia

机构信息

Institute for Quantum Science and Technology, International Centre of Quantum and Molecular Structures, State Key Laboratory of Advanced Special Steel, Shanghai Key Laboratory of High Temperature Superconductors, Physics Department, Shanghai University, Shanghai 200444, China.

Consiglio Nazionale delle Ricerche (CNR-SPIN), Unità di Ricerca presso Terzo di Chieti, c/o Università G. D'Annunzio, I-66100 Chieti, Italy.

出版信息

Phys Rev Lett. 2024 Feb 23;132(8):086802. doi: 10.1103/PhysRevLett.132.086802.

Abstract

Driven by the expected contribution of two-dimensional multiferroic systems with strong magnetoelectric coupling to the development of multifunctional nanodevices, here we propose, by means of first-principles calculations, vanadium-halide monolayers as a new class of spin-chirality-driven van der Waals multiferroics. The frustrated 120-deg magnetic structure in the triangular lattice induces a ferroelectric polarization perpendicular to the spin-spiral plane, whose sign is switched by a spin-chirality change. It follows that, in the presence of an applied electric field perpendicular to the monolayers, one magnetic chirality can be stabilized over the other, thereby allowing the long-sought electrical control of spin textures. Moreover, we demonstrate the remarkable role of spin-lattice coupling on magnetoelectricity, which adds to the expected contribution of spin-orbit interaction determined by an anion. Indeed, such compounds exhibit sizeable spin-driven structural distortions, thereby promoting the investigation of multifunctional spin-electric-lattice couplings.

摘要

受二维多铁性系统通过强磁电耦合对多功能纳米器件发展的预期贡献驱动,在此我们通过第一性原理计算提出,卤化钒单层作为一类新型的自旋手性驱动的范德华多铁性材料。三角晶格中受挫的120度磁结构会诱导出垂直于自旋螺旋平面的铁电极化,其符号会通过自旋手性的改变而切换。由此可知,在存在垂直于单层施加的电场时,一种磁手性可以比另一种更稳定,从而实现长期以来寻求的对自旋纹理的电控制。此外,我们证明了自旋 - 晶格耦合对磁电效应的显著作用,这补充了由阴离子决定的自旋 - 轨道相互作用的预期贡献。实际上,这类化合物表现出相当大的自旋驱动结构畸变,从而推动了对多功能自旋 - 电 - 晶格耦合的研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验