催化作用
聚苯胺
选择性
法拉第效率
材料科学
铜
化学工程
过渡金属
二氧化碳电化学还原
电化学
涂层
无机化学
基质(水族馆)
乙烯
氧化还原
化学
一氧化碳
纳米技术
聚合物
有机化学
电极
冶金
物理化学
复合材料
地质学
聚合
海洋学
工程类
作者
Wei Xing,Zhenglei Yin,Kangjie Lyu,Zhen Li,Jun Gong,Gongwei Wang,Li Xiao,Juntao Lu,Lin Zhuang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-03-05
卷期号:10 (7): 4103-4111
被引量:289
标识
DOI:10.1021/acscatal.0c00049
摘要
Electrochemical reduction of carbon dioxide (CO2RR) to liquid fuels and valued chemicals is a meaningful approach to decreasing CO2 emissions and alleviating the energy crisis. In particular, the conversion of CO2 into multicarbon products is of technological significance. Cu is the only transition metal that is able to catalyze the CO2RR to produce C2+ hydrocarbons, but the catalytic selectivity of pristine Cu is low. Herein we report a facile method to largely enhance the C2+ selectivity of polycrystalline Cu toward the CO2RR. By coating the Cu surface with a 50 nm thick film of polyaniline (PANI), the faradaic efficiency (FE) of C2+ hydrocarbons was increased from ca. 15% to 60% at −1.1 VRHE in KHCO3 solutions. When applying the PANI coating onto Cu nanoparticles, the FE of C2+ hydrocarbons can even reach 80%, with the FE of ethylene over 40%. Such performance remained stable in a test period of 20 h. The superiority of the Cu/PANI interface is not due to the change in the morphology or the electronic properties of the Cu substrate but instead is due to an improvement in the coverage and interaction of the CO intermediate, which facilitates the CO–CO coupling, as revealed by in situ infrared spectroscopy. This study opens an avenue to tuning the catalytic activity and selectivity of Cu toward the CO2RR, not through the structure of the catalyst but through the environment above the surface.
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