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

Author:

Han Shitao12,Xia Wei12,Jia Shuaiqiang12,Yao Ting12,Jiao Jiapeng12,Wang Min12,Dong Xue12,Yang Jiahao12,Zhou Dawei12,He Mingyuan12,Wu Haihong12,Han Buxing123ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes School of Chemistry and Molecular Engineering East China Normal University Shanghai 200062 P. R. China

2. Institute of Eco-Chongming Chenjia Town, Chongming District Shanghai 202162 P. R. China

3. Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Colloid and Interface and Thermodynamics CAS Research/Education Center for Excellence in Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China

Abstract

AbstractThe 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.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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