首页|Electrochemical CO2 reduction to C2+products over Cu/Zn intermetallic catalysts synthesized by electrodeposition

Electrochemical CO2 reduction to C2+products over Cu/Zn intermetallic catalysts synthesized by electrodeposition

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Electrocatalytic CO2 reduction(ECR)offers an attractive approach to realizing carbon neutrality and producing valuable chemicals and fuels using CO2 as the feedstock.However,the lack of cost-effective electroca-talysts with better performances has seriously hindered its application.Herein,a one-step co-electrodeposition method was used to introduce Zn,a metal with weak*CO binding energy,into Cu to form Cu/Zn intermetallic catalysts(Cu/Zn IMCs).It was shown that,using an H-cell,the high Faradaic efficiency of C2+hydrocarbons/alcohols(FEC2+)could be achieved in ECR by adjusting the surface metal components and the applied potential.In suitable conditions,FEC2+and current density could be as high as 75%and 40 mA/cm2,respectively.Compared with the Cu catalyst,the Cu/Zn IMCs have a lower interfacial charge transfer resistance and a larger electrochemically active surface area(ECSA),which accelerate the reaction.Moreover,the*CO formed on Zn sites can move to Cu sites due to its weak binding with*CO,and thus enhance the C-C coupling on the Cu surface to form C2+products.

carbon dioxide electroreductionelectrochemistryco-electrodepositionintermetallic catalystsvalue-added chemicals

Ting DENG、Shuaiqiang JIA、Shitao HAN、Jianxin ZHAI、Jiapeng JIAO、Xiao CHEN、Cheng XUE、Xueqing XING、Wei XIA、Haihong WU、Mingyuan HE、Buxing HAN

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School of Chemistry and Molecular Engineering,East China Normal University,Shanghai 200062,China

Institute of Eco-Chongming,Shanghai 202162,China

Institute of High Energy Physics,Chinese Academy of Sciences,Beijing 100049,China

Institute of Chemistry,Chinese Academy of Sciences,Beijing 100190,China

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国家重点研发计划中国博士后科学基金国家自然科学基金国家自然科学基金国家自然科学基金Research Funds of Happiness Flower ECNU

2020YFA07102012023M7310962202230722121002218907612020ST2203

2024

能源前沿
高等教育出版社

能源前沿

CSTPCDEI
影响因子:0.2
ISSN:2095-1701
年,卷(期):2024.18(1)
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