自旋电子学
价电子
电子
密度泛函理论
价(化学)
电子结构
材料科学
凝聚态物理
赫巴德模型
化学物理
化学
物理
计算化学
铁磁性
量子力学
超导电性
作者
Dhaneesh Kumar,Jack Hellerstedt,B.O. Field,Benjamin Löwe,Yuefeng Yin,Nikhil V. Medhekar,Agustin Schiffrin
标识
DOI:10.1002/adfm.202106474
摘要
Abstract 2D and layered electronic materials characterized by a kagome lattice, whose valence band structure includes two Dirac bands and one flat band, can host a wide range of tunable topological and strongly correlated electronic phases. While strong electron correlations have been observed in inorganic kagome crystals, they remain elusive in organic systems, which benefit from versatile synthesis protocols via molecular self‐assembly and metal‐ligand coordination. Here, direct experimental evidence of local magnetic moments resulting from strong electron–electron Coulomb interactions in a 2D metal–organic framework (MOF) is reported. The latter consists of di‐cyano‐anthracene (DCA) molecules arranged in a kagome structure via coordination with copper (Cu) atoms on a silver surface [Ag(111)]. Temperature‐dependent scanning tunneling spectroscopy reveals magnetic moments spatially confined to DCA and Cu sites of the MOF, and Kondo screened by the Ag(111) conduction electrons. By density functional theory and mean‐field Hubbard modeling, it is shown that these magnetic moments are the direct consequence of strong Coulomb interactions between electrons within the kagome MOF. The findings pave the way for nanoelectronics and spintronics technologies based on controllable correlated electron phases in 2D organic materials.
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