范德瓦尔斯力
凝聚态物理
激子
物理
联轴节(管道)
磁电机
范德瓦尔斯株
感应耦合
材料科学
范德瓦尔斯半径
量子力学
分子
功率(物理)
冶金
作者
Jia Shi,Hui‐Tian Wang,Nai Jiang,Zhiduo Xin,Houzhi Zheng,Chao Shen,Xinping Zhang,Xinfeng Liu
标识
DOI:10.48550/arxiv.2409.18437
摘要
Controlling magnetic order via external fields or heterostructures enables precise manipulation and tracking of spin and exciton information, facilitating the development of high-performance optical spin valves. However, the weak magneto-optical signals and instability of two dimensional (2D) antiferromagnetic (AFM) materials have hindered comprehensive studies on the complex coupling between magnetic order and excitons in bulk-like systems. Here, we leverage magneto-optical spectroscopy to reveal the impact of magnetic order on exciton-phonon coupling and exciton-magnetic order coupling which remains robust even under non-extreme temperature conditions (80 K) in thick layered CrSBr. A 0.425T in-plane magnetic field is sufficient to induce spin flipping and transition from AFM to ferromagnetic (FM) magnetic order in CrSBr, while magnetic circular dichroism (MCD) spectroscopy under an out-of-plane magnetic field provides direct insight into the complex spin canting behavior in thicker layers. Theoretical calculations reveal that the strong coupling between excitons and magnetic order, especially the 32 meV exciton energy shift during magnetic transitions, stems from the hybridization of Cr and S orbitals and the larger exciton wavefunction radius of higher-energy B excitons. These findings offer new opportunities and a solid foundation for future exploration of 2D AFM materials in magneto-optical sensors and quantum communication using excitons as spin carriers.
科研通智能强力驱动
Strongly Powered by AbleSci AI