化学
双金属片
过电位
铋
法拉第效率
电催化剂
格式化
铜
选择性
催化作用
二氧化碳电化学还原
可逆氢电极
无机化学
电极
电化学
工作电极
一氧化碳
有机化学
物理化学
作者
Jia Lin,Hui Yang,Jun Deng,Junmei Chen,Yuan Zhou,Ding Pan,Leigang Li,Ning Han,Yanguang Li
标识
DOI:10.1002/cjoc.201900010
摘要
Summary of main observation and conclusion Electrocatalytic carbon dioxide reduction holds great promise for reducing the atmospheric CO 2 level and alleviating the energy crisis. High‐performance electrocatalysts are often required in order to lower the high overpotential and expedite the sluggish reaction kinetics of CO 2 electroreduction. Copper is a promising candidate metal. However, it usually suffers from the issues of poor stability and low product selectivity. In this work, bimetallic Cu‐Bi is obtained by reducing the microspherical copper bismuthate (CuBi 2 O 4 ) for selectively catalyzing the CO 2 reduction to formate (HCOO – ). The bimetallic Cu‐Bi electrocatalyst exhibits high activity and selectivity with the Faradic efficiency over 90% in a wide potential window. A maximum Faradaic efficiency of ~95% is obtained at –0.93 V versus reversible hydrogen electrode. Furthermore, the catalyst shows high stability over 6 h with Faradaic efficiency of ~95%. This study provides an important clue in designing new functional materials for CO 2 electroreduction with high activity and selectivity.
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