A Bismuth‐Based Zeolitic Organic Framework with Coordination‐Linked Metal Cages for Efficient Electrocatalytic CO₂ Reduction to HCOOH

Abstract

Zeolitic metal-organic frameworks (ZMOFs) have emerged as one of the most promsing catalysts for energy conversion, but they suffer from either weak bonding between metal-organic cubes (MOCs) that decrease their stability during catalysis processes or low activity due to inadequate active sites. In this work, through ligand-directing strategy, we successfully obtain an unprecedented bismuth-based ZMOF (Bi-ZMOF) featuring a ACO topological crystal structure with strong coordination bonding between the Bi-based cages. As a result, it enables efficient reduction of CO₂ to formic acid (HCOOH) with Faradaic efficiency as high as 91 %. A combination of in situ surface-enhanced infrared absorption spectroscopy and density functional theory calculation reveals that the Bi-N coordination contributes to facilitating charge transfer from N to Bi atoms, which stabilize the intermediate to boost the reduction efficiency of CO₂ to HCOOH. This finding highlights the importance of the coordination environment of metal active sites on electrocatalytic CO₂ reduction. We believe that this work will offer a new clue to rationally design zeolitic MOFs for catalytic reaction.