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Keeping sight of copper in single-atom catalysts for electrochemical carbon dioxide reduction

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  • Charles E. Creissen

    (Collège de France)

  • Marc Fontecave

    (Collège de France)

Abstract

Carbon dioxide can be electrochemically converted into valuable multi-carbon products using Cu-based single-atom catalysts. However, transient cluster formation, which is undetectable using ex-situ techniques, may be responsible for C2+ products. Here we discuss these observations to highlight the need for operando characterisation when defining active sites.

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  • Charles E. Creissen & Marc Fontecave, 2022. "Keeping sight of copper in single-atom catalysts for electrochemical carbon dioxide reduction," Nature Communications, Nature, vol. 13(1), pages 1-4, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30027-x
    DOI: 10.1038/s41467-022-30027-x
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    1. Jiqing Jiao & Qing Yuan & Meijie Tan & Xiaoqian Han & Mingbin Gao & Chao Zhang & Xuan Yang & Zhaolin Shi & Yanbin Ma & Hai Xiao & Jiangwei Zhang & Tongbu Lu, 2023. "Constructing asymmetric double-atomic sites for synergistic catalysis of electrochemical CO2 reduction," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Yizhou Dai & Huan Li & Chuanhao Wang & Weiqing Xue & Menglu Zhang & Donghao Zhao & Jing Xue & Jiawei Li & Laihao Luo & Chunxiao Liu & Xu Li & Peixin Cui & Qiu Jiang & Tingting Zheng & Songqi Gu & Yao , 2023. "Manipulating local coordination of copper single atom catalyst enables efficient CO2-to-CH4 conversion," Nature Communications, Nature, vol. 14(1), pages 1-12, December.

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