材料科学
磁性
铁磁性
自旋电子学
离子键合
磁晶各向异性
中子衍射
范德瓦尔斯力
化学物理
凝聚态物理
离子
居里温度
结晶学
磁化学
过渡金属
硫代磷酸盐
反铁磁性
铜
磁各向异性
石墨烯
铁磁性
磁矩
简并能级
抗磁性
四极分裂
各向异性
磁性结构
作者
Ruichen Xie,Zhongchong Lin,Yan Cao,Chao Yun,Zhi Zhang,Shaohua Fan,Yuxuan Peng,Xiaobai Ma,K. Li,Caijuan Shi,Dong Zhou,Rui Han,H P Du,Xiaoxi Liu,Zhaochu Luo,Jinbo Yang,Wenyun Yang
标识
DOI:10.1002/adma.202520850
摘要
ABSTRACT Two‐dimensional (2D) van der Waals (vdW) magnets offer a versatile platform to explore fundamental physics and low‐dimensional functionalities. Metal thiophosphates (MTPs) with mobile Cu + ions exhibit a ferroionic state, where polarization arises from ionic redistribution among multiple nearly degenerate sites. CuVP 2 S 6 uniquely combines intrinsic ferromagnetism from the V sublattice with Cu + ‐driven ferroionic configurational freedom, enabling direct exploration of how ionic dynamics influence magnetic interactions. Herein, high‐quality CuVP 2 S 6 single crystals are synthesized, and their structural and physical properties are systematically investigated. Temperature‐dependent neutron diffraction elucidates a ferroionic structure with dynamic distributions of copper ions across multiple crystallographic sites. The versatile occupations are driven by local symmetry‐controlled orbital interactions between copper ions and surrounding ligands through a second‐order Jahn–Teller mechanism. Magnetic measurements identify a ferromagnetic (FM) transition below 3.3 K. The pressure‐controlled magnetocrystalline anisotropy and interlayer exchange interactions mediated by Cu + migration are demonstrated, boosting the Curie temperature remarkably by over 60% and inducing a soft‐to‐hard FM transition unparalleled within the MTP family. These results demonstrate that ionic configurational freedom provides an efficient route to control magnetism, opening new possibilities for spintronic applications.
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