Light-Controlled Ultrafast Magnetic State Transition in Antiferromagnetic-Ferromagnetic van der Waals Heterostructures

被引:10
|
作者
Li, Shuo [1 ]
Zhou, Liujiang [2 ]
Frauenheim, Thomas [3 ,5 ]
He, Junjie [4 ,6 ]
机构
[1] Chengdu Univ, Inst Adv Study, Chengdu 610100, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Phys, Chengdu 610054, Peoples R China
[3] Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R China
[4] Univ Bremen, Bremen Ctr Computat Mat Sci, D-28359 Bremen, Germany
[5] Shenzhen JL Computat Sci & Appl Res Inst, Shenzhen 518110, Peoples R China
[6] Charles Univ Prague, Fac Sci, Dept Phys & Macromol Chem, Prague 12843, Czech Republic
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2022年 / 13卷 / 26期
关键词
SE;
D O I
10.1021/acs.jpclett.2c01476
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
Manipulating spin in antiferromagnetic (AFM) materials has great potential in AFM opto-spintronics. Laser pulses can induce a transient ferromagnetic (FM) state in AFM metallic systems but have never been proven in two-dimensional (2D) AFM semiconductors and related van der Waals (vdW) heterostructures. Herein, using 2D vdW heterostructures of FM MnS2 and AFM MXenes as prototypes, we investigated optically induced interlayer spin transfer dynamics based on real-time time-dependent density functional theory. We observed that laser pulses induce significant spin injection and interfacial atom-mediated spin transfer from MnS2 to Cr2CCl2. In particular, we first demonstrated the transient FM state in semiconducting AFM-FM heterostructures during photoexcited processes. The proximity magnetism breaks the magnetic symmetry of Cr2CCl2 in heterostructures. Our results provide a microscopic understanding of optically controlled interlayer spin dynamics in 2D magnetic heterostructures and open a new way to manipulate magnetic order in 2D materials for ultrafast opto-spintronics.
引用
收藏
页码:6223 / 6229
页数:7
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