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Unveiling hydrocerussite as an electrochemically stable active phase for efficient carbon dioxide electroreduction to formate.


ABSTRACT: For most metal-containing CO2 reduction reaction (CO2RR) electrocatalysts, the unavoidable self-reduction to zero-valence metal will promote hydrogen evolution, hence lowering the CO2RR selectivity. Thus it is challenging to design a stable phase with resistance to electrochemical self-reduction as well as high CO2RR activity. Herein, we report a scenario to develop hydrocerussite as a stable and active electrocatalyst via in situ conversion of a complex precursor, tannin-lead(II) (TA-Pb) complex. A comprehensive characterization reveals the in situ transformation of TA-Pb to cerussite (PbCO3), and sequentially to hydrocerussite (Pb3(CO3)2(OH)2), which finally serves as a stable and active phase under CO2RR condition. Both experiments and theoretical calculations confirm the high activity and selectivity over hydrocerussite. This work not only offers a new approach of enhancing the selectivity in CO2RR by suppressing the self-reduction of electrode materials, but also provides a strategy for studying the reaction mechanism and active phases of electrocatalysts.

SUBMITTER: Shi Y 

PROVIDER: S-EPMC7343827 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Unveiling hydrocerussite as an electrochemically stable active phase for efficient carbon dioxide electroreduction to formate.

Shi Yanmei Y   Ji Yan Y   Long Jun J   Liang Yu Y   Liu Yang Y   Yu Yifu Y   Xiao Jianping J   Zhang Bin B  

Nature communications 20200708 1


For most metal-containing CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) electrocatalysts, the unavoidable self-reduction to zero-valence metal will promote hydrogen evolution, hence lowering the CO<sub>2</sub>RR selectivity. Thus it is challenging to design a stable phase with resistance to electrochemical self-reduction as well as high CO<sub>2</sub>RR activity. Herein, we report a scenario to develop hydrocerussite as a stable and active electrocatalyst via in situ conversion of a compl  ...[more]

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