过电位
选择性
材料科学
纳米线
催化作用
电解质
化学工程
电催化剂
法拉第效率
吸附
纳米技术
无机化学
电化学
化学
电极
物理化学
有机化学
工程类
作者
Jinze Liu,Yating Wang,Hao Jiang,Haibo Jiang,Xiaodong Zhou,Yuhang Li,Chunzhong Li
标识
DOI:10.1002/asia.201901550
摘要
Abstract Electrochemical reduction of carbon dioxide (CO2) to CO is regarded as an efficient method to utilize the greenhouse gas CO2, because the CO product can be further converted into high value‐added chemicals via the Fisher–Tropsch process. Among all electrocatalysts used for CO2‐to‐CO reduction, Au‐based catalysts have been demonstrated to possess high selectivity, but their precious price limits their future large‐scale applications. Thus, simultaneously achieving high selectivity and reasonable price is of great importance for the development of Au‐based catalysts. Here, we report Ag@Au core–shell nanowires as electrocatalyst for CO2 reduction, in which a nanometer‐thick Au film is uniformly deposited on the core Ag nanowire. Importantly, the Ag@Au catalyst with a relative low Au content can drive CO generation with nearly 100 % Faraday efficiency in 0.1 m KCl electrolyte at an overpotential of ca. −1.0 V. This high selectivity of CO2 reduction could be attributed to a suitable adsorption strength for the key intermediate on Au film together with the synergistic effects between the Au shell and Ag core and the strong interaction between CO2 and Cl− ions in the electrolyte, which may further pave the way for the development of high‐efficiency electrocatalysts for CO2 reduction.
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