| Literature DB >> 33978299 |
Ping Shao1, Wei Zhou2, Qin-Long Hong1, Luocai Yi1, Lirong Zheng3, Wenjing Wang1, Hai-Xia Zhang1, Huabin Zhang4, Jian Zhang1.
Abstract
Fundamental understanding of the dependence between the structure and composition on the electrochemical CO2 reduction reaction (CO2 RR) would guide the rational design of highly efficient and selective electrocatalysts. A major impediment to the deep reduction CO2 to multi-carbon products is the complexity of carbon-carbon bond coupling. The chemically well-defined catalysts with atomically dispersed dual-metal sites are required for these C-C coupling involved processes. Here, we developed a catalyst (BIF-102NSs) that features Cl- bridged dimer copper (Cu2 ) units, which delivers high catalytic activity and selectivity for C2 H4 . Mechanistic investigation verifies that neighboring Cu monomers not only perform as regulator for varying the reaction barrier, but also afford distinct reaction paths compared with isolated monomers, resulting in greatly improved electroreduction performance for CO2 .Entities:
Keywords: CO2 reduction; catalysts; crystal; electrocatalysis; metal-organic frameworks
Year: 2021 PMID: 33978299 DOI: 10.1002/anie.202106004
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336