Exchange Coupling-Induced Giant Spin Splitting in Two-Dimensional M2X3/TMD Heterostructures

被引:0
|
作者
Yan, Jingshen [1 ]
Chen, Kaixuan [1 ,2 ]
Lyu, Shu-Shen [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Mat, Shenzhen Campus, Shenzhen 518107, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Engn Technol Res Ctr, Adv Thermal Control Mat & Syst Integrat ATCMSI, Guangzhou 510275, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 46期
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; ULTRASOFT PSEUDOPOTENTIALS; MAGNETS;
D O I
10.1021/acs.jpcc.4c05339
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-dimensional (2D) magnet-insulator heterostructures have shown potential as promising platforms for tuning valleytronics and spintronics. Thanks to their two-dimensional nature, possible candidates for realizing even richer quantum phases have been extended to a huge family of materials. Targeting the search for heterostructures with better performance, we suggest a Dirac electronic system M2X3 (M = transition metal, X = O/S) coupled with transition metal dichalcogenides (TMDs) as a new heterostructure family. We conduct a systematic first-principles study on electronic band properties and magnetic properties of M2X3/TMD heterostructures. On this ground, we reveal that there exists a giant spin splitting larger than the previously reported Cr-based system and identify the origin of this giant spin splitting as exchange coupling in this heterostructure. The efficient Zeeman field is up to 580 T in Cr2O3/WS2. Our study suggests that M2X3/TMD can be a potential platform for realizing skyrmions. Due to its advantage as a simpler structure and a Dirac electronic system over the reported CrI3 family in realization of such a spin system, M2X3/TMD holds the promise of discovering even richer quantum phases within the system.
引用
收藏
页码:19856 / 19865
页数:10
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