凝聚态物理
自旋电子学
磁性
扫描隧道显微镜
范德瓦尔斯力
单层
自旋(空气动力学)
石墨烯
密度泛函理论
双层
自旋极化
双层石墨烯
原子单位
六边形晶格
材料科学
物理
反铁磁性
纳米技术
化学
铁磁性
量子力学
生物化学
膜
热力学
分子
电子
作者
Mao-Peng Miao,Nanshu Liu,Wenhao Zhang,Jian-Wang Zhou,D. S. Wang,Cong Wang,Wei Ji,Ying‐Shuang Fu
标识
DOI:10.1073/pnas.2422868122
摘要
Noncollinear magnetic orders in monolayer van der Waals magnets are crucial for probing delicate magnetic interactions under minimal spatial constraints and advancing miniaturized spintronic devices. Despite their significance, achieving atomic-scale identification remains challenging. In this study, we utilized spin-polarized scanning tunneling microscopy and density functional theory calculations to identify spin-spiral orders in mono- and bilayer NiI 2 , grown on graphene-covered SiC(0001) substrates. We found two distinct spin-spiral states with Q vectors aligning and deviating by 7° from the lattice direction, exhibiting periodicities of 4.54 and 5.01 times the lattice constant, respectively. These findings contrast with bulk properties and align closely with our theoretical calculations. Surprisingly, the nonmultiples of spin spirals within finite-sized magnetic domains induce net magnetic moments, facilitating collective spin switching behavior under magnetic fields. Our research reveals intrinsic noncollinear magnetism at the monolayer limit with atomic-scale resolution, paving the way for exploring spin phenomena.
科研通智能强力驱动
Strongly Powered by AbleSci AI