催化作用
咪唑酯
二聚体
铜
沸石咪唑盐骨架
纳米片
单体
碳纤维
无机化学
化学
选择性
硼
材料科学
电化学
乙烯
金属
金属有机骨架
纳米技术
电极
吸附
有机化学
物理化学
聚合物
复合数
复合材料
作者
Ping Shao,Wei Zhou,Qin‐Long Hong,Luocai Yi,Lirong Zheng,Wenjing Wang,Hai‐Xia Zhang,Huabin Zhang,Jian Zhang
标识
DOI:10.1002/anie.202106004
摘要
Abstract Fundamental understanding of the dependence between the structure and composition on the electrochemical CO 2 reduction reaction (CO 2 RR) would guide the rational design of highly efficient and selective electrocatalysts. A major impediment to the deep reduction CO 2 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 (Cu 2 ) units, which delivers high catalytic activity and selectivity for C 2 H 4 . 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 CO 2 .
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