Abstract
Construction of metal–organic cages (MOCs) with internal modifications is a promising avenue to build enzyme‐like cavities and unlocking the mystery of highly catalytic activity and selectivity of enzymes. However, current interests are mainly focused on single‐metal‐node cages, little achievement has been expended to metalloclusters‐based architectures, and the in situ endogenous generation of metal clusters. Herein, based on the hard‐soft‐acids‐bases (HSAB), the metalloclusters‐based heterometallic MOC (Cu3VMOP) constructed of [Cu3OPz3]+ and [V6O6(OCH3)9(SO4)(CO2)3]2– clusters was obtained by one‐pot method. In addition, Cu4I4 was generated in situ in the cage to form Cu4I4@Cu3VMOP by the coordination‐driven hierarchical self‐assembly strategy. As catalysts for CO2 reduction, Cu3VMOP produces HCOOH and CH3COOH as the main reduction product with yield of CH3COOH up to 0.9 mmol g–1, ranking among the highest value of reported materials, whereas Cu4I4@Cu3VMOP exhibited targeted CO2‐to‐HCOOH conversion with 100% formic acid selectivity and the yield outperforms that of Cu3VMOP by 5 fold. Theoretical calculations and femtosecond time‐resolved transient absorption reveal that endogenous Cu4I4 not only regulates orbital arrangements and enhances localized electron states to generate a long‐lived charge‐separated state, but also raises *CO coupling energy barrier, resulting in the targeted conversion of CO2 to formic acid.
Published Version
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