三元运算
乙烯
催化作用
基质(水族馆)
材料科学
化学工程
碳纤维
纳米技术
无机化学
化学
有机化学
海洋学
复合数
计算机科学
工程类
复合材料
程序设计语言
地质学
作者
Likun Xiong,Xiang Zhang,Hao Yuan,Juan Wang,Xuzhou Yuan,Yuebin Lian,Huidong Jin,Hao Sun,Zhao Deng,Dan Wang,Jiapeng Hu,Huimin Hu,Jin‐Ho Choi,Jiong Li,Yufeng Chen,Jun Zhong,Jun Guo,Mark H. Rümmerli,Lai Xu,Yang Peng
标识
DOI:10.1002/ange.202012631
摘要
Abstract Electrocatalytic conversion of carbon dioxide into high‐value multicarbon (C 2+ ) chemical feedstocks offers a promising avenue to liberate the chemical industry from fossil‐resource dependence and eventually close the anthropogenic carbon cycle but is severely impeded by the lack of high‐performance catalysts. To break the linear scaling relationship of intermediate binding and minimize the kinetic barrier of CO 2 reduction reactions, ternary Cu–Au/Ag nanoframes were fabricated to decouple the functions of CO generation and C−C coupling, whereby the former is promoted by the alloyed Ag/Au substrate and the latter is facilitated by the highly strained and positively charged Cu domains. Thus, C 2 H 4 production in an H‐cell and a flow cell occurred with high Faradic efficiencies of 69±5 and 77±2 %, respectively, as well as good electrocatalytic stability and material durability. In situ IR and DFT calculations unveiled two competing pathways for C 2 H 4 generation, of which direct CO dimerization is energetically favored.
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