电子结构
材料科学
化学物理
原子轨道
电子能带结构
金属有机骨架
纳米技术
金属
过渡金属
带隙
电子组态
计算化学
化学
凝聚态物理
光电子学
电子
离子
物理
物理化学
有机化学
吸附
量子力学
冶金
催化作用
作者
Simone Mearini,Daniel Baranowski,Dominik Brandstetter,Andreas Windischbacher,Iulia Cojocariu,Pierluigi Gargiani,Manuel Valvidares,Luca Schio,Luca Floreano,Peter Puschnig,Vitaliy Feyer,Claus M. Schneider
标识
DOI:10.1002/advs.202404667
摘要
The design of 2D metal-organic frameworks (2D MOFs) takes advantage of the combination of the diverse electronic properties of simple organic ligands with different transition metal (TM) centers. The strong directional nature of the coordinative bonds is the basis for the structural stability and the periodic arrangement of the TM cores in these architectures. Here, direct and clear evidence that 2D MOFs exhibit intriguing energy-dispersive electronic bands with a hybrid character and distinct magnetic properties in the metal cores, resulting from the interactions between the TM electronic levels and the organic ligand π-molecular orbitals, is reported. Importantly, a method to effectively tune both the electronic structure of 2D MOFs and the magnetic properties of the metal cores by exploiting the electronic structure of distinct TMs is presented. Consequently, the ionization potential characteristic of selected TMs, particularly the relative energy position and symmetry of the 3d states, can be used to strategically engineer bands within specific metal-organic frameworks. These findings not only provide a rationale for band structure engineering in 2D MOFs but also offer promising opportunities for advanced material design.
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