铁磁性
旋转
凝聚态物理
材料科学
实现(概率)
单层
居里温度
磁滞
金属
各向异性
磁矩
化学物理
纳米技术
物理
量子力学
数学
统计
冶金
作者
Jorge Lobo‐Checa,Leyre Hernández-López,M. M. Otrokov,Ignacio Piquero‐Zulaica,Adriana E. Candia,Pierluigi Gargiani,David Serrate,F.S. Delgado,Manuel Valvidares,Jorge I. Cerdá,A. Arnau,F. Bartolomé
标识
DOI:10.1038/s41467-024-46115-z
摘要
Abstract Ferromagnetism is the collective alignment of atomic spins that retain a net magnetic moment below the Curie temperature, even in the absence of external magnetic fields. Reducing this fundamental property into strictly two-dimensions was proposed in metal-organic coordination networks, but thus far has eluded experimental realization. In this work, we demonstrate that extended, cooperative ferromagnetism is feasible in an atomically thin two-dimensional metal-organic coordination network, despite only ≈ 5% of the monolayer being composed of Fe atoms. The resulting ferromagnetic state exhibits an out-of-plane easy-axis square-like hysteresis loop with large coercive fields over 2 Tesla, significant magnetic anisotropy, and persists up to T C ≈ 35 K. These properties are driven by exchange interactions mainly mediated by the molecular linkers. Our findings resolve a two decade search for ferromagnetism in two-dimensional metal-organic coordination networks.
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