CO2 Electroreduction to C2+ Products over Cu-Pb Heterojunction Catalyst

被引:4
|
作者
Han, Shitao [1 ,2 ]
Xia, Wei [1 ,2 ]
Jia, Shuaiqiang [1 ,2 ]
Yao, Ting [1 ,2 ]
Jiao, Jiapeng [1 ,2 ]
Wang, Min [1 ,2 ]
Dong, Xue [1 ,2 ]
Yang, Jiahao [1 ,2 ]
Zhou, Dawei [1 ,2 ]
He, Mingyuan [1 ,2 ]
Wu, Haihong [1 ,2 ]
Han, Buxing [1 ,2 ,3 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[2] Inst Ecochongming, Shanghai 202162, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Key Lab Colloid & Interface & Thermodynam, CAS Res Educ Ctr Excellence Mol Sci,Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2 Reduction Reaction; Cu-based catalyst; Heterojunction Catalyst; Pb; Multicarbon Products; REDUCTION;
D O I
10.1002/cctc.202300918
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical CO2 reduction reaction (CO2RR) presents a promising approach for producing valuable chemicals and fuels, offering a dual benefit in terms of environmental preservation and the efficient utilization of carbon resources. In this work, we proposed a stepwise electrodeposition method to prepare Cu-Pb bimetallic heterojunction catalyst on polyaniline-modified carbon paper (PANI-CuPb-x), where x is the electrodeposition times(min). Among the studied catalysts, the electrode electrodeposited for 2 min (PANI-CuPb-2) exhibited a remarkable performance during the electrocatalysis CO2 to multicarbon (C2+) products process, achieving a Faraday efficiency (FE) of 81.46 % and a partial current density of 15.41 mA cm(-2) at -1.2 V (vs. RHE) in an H-type cell. The detailed study demonstrated that introducing Pb could effectively improve the formation of COOH*inhibit hydrogen evolution reaction (HER). Furthermore, the heterojunction structure in the catalysts facilitated C-C coupling of the generated C1 intermediate species, which enhanced the CO2 to C2+ reaction.
引用
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页数:7
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