Doping engineering of Cu-based catalysts for electrocatalytic CO2 reduction to multi-carbon products

The electrocatalytic carbon dioxide reduction reaction (CO2RR) is a promising technology that uses renewable energy sources to convert excess atmospheric CO2 into high-value multi-carbon (C2+) products. In the CO2RR mechanism, adsorbed *CO is recognized as a crucial intermediate, playing a pivotal r...

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Published inEnergy & environmental science Vol. 17; no. 16; pp. 5795 - 5818
Main Authors You, Shiya, Xiao, Jiewen, Liang, Shuyu, Xie, Wenfu, Zhang, Tianyu, Li, Min, Zhong, Ziyi, Wang, Qiang, He, Hong
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 13.08.2024
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Summary:The electrocatalytic carbon dioxide reduction reaction (CO2RR) is a promising technology that uses renewable energy sources to convert excess atmospheric CO2 into high-value multi-carbon (C2+) products. In the CO2RR mechanism, adsorbed *CO is recognized as a crucial intermediate, playing a pivotal role in facilitating the formation of C2+ products. Currently, Cu-based materials are the most effective catalysts in producing *CO and further coupling it to form C2+ products. However, mono-component Cu catalysts still face some challenges, such as low activity, selectivity, and poor stability. Doping engineering has emerged as a valuable strategy for enhancing the performance of Cu-based catalysts in CO2 electroreduction into C2+ products. This comprehensive review presents the recent advancements in CO2 electroreduction into C2+ products over heteroatom-doped Cu-based catalysts, encompassing metallic heteroatoms such as Pd, Au and Ag, as well as non-metallic heteroatoms like P, B and F. The mechanism of enhanced performance through heteroatom doping is specifically highlighted, providing helpful guidance and avenues for the rational design of Cu-based catalysts. Additionally, the review discusses the challenges and prospects associated with the CO2RR into C2+ products, offering a nuanced perspective on this subject.
ISSN:1754-5692
1754-5706
DOI:10.1039/d4ee01325e