一氧化碳
铜
法拉第效率
电化学
选择性
材料科学
电解质
化学工程
无机化学
电催化剂
化学
二氧化碳电化学还原
电极
冶金
有机化学
催化作用
物理化学
工程类
作者
Wesley Luc,Xianbiao Fu,Jianjian Shi,Jing Lv,Matthew Jouny,Byung Hee Ko,Yaobin Xu,Qing Tu,Xiaobing Hu,Jinsong Wu,Qin Yue,Yuanyue Liu,Feng Jiao,Yijin Kang
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2019-04-08
卷期号:2 (5): 423-430
被引量:444
标识
DOI:10.1038/s41929-019-0269-8
摘要
Upgrading carbon dioxide to high-value multicarbon (C2+) products is one promising avenue for fuel and chemical production. Among all the monometallic catalysts, copper has attracted much attention because of its unique ability to convert CO2 or CO into C2+ products with an appreciable selectivity. Although numerous attempts have been made to synthesize Cu materials that expose the desired facets, it still remains a challenge to obtain high-quality nanostructured Cu catalysts for the electroreduction of CO2/CO. Here we report a facile synthesis of freestanding triangular-shaped two-dimensional Cu nanosheets that selectively expose the (111) surface. In a 2 M KOH electrolyte, the Cu nanosheets exhibit an acetate Faradaic efficiency of 48% with an acetate partial current density up to 131 mA cm−2 in electrochemical CO reduction. Further analysis suggest that the high acetate selectivity is attributed to the suppression of ethylene and ethanol formation, probably due to the reduction of exposed (100) and (110) surfaces. Upgrading CO to high-value multicarbon products is a promising avenue for fuel and chemical feedstock production. Here triangular Cu nanosheets that selectively expose the (111) surface exhibit a high acetate partial current density (131 mA cm–2) and Faradaic efficiency (48%) in CO electroreduction.
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