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Electrochemical CO2 reduction to ethylene by ultrathin CuO nanoplate arrays.


ABSTRACT: Electrochemical reduction of CO2 to multi-carbon fuels and chemical feedstocks is an appealing approach to mitigate excessive CO2 emissions. However, the reported catalysts always show either a low Faradaic efficiency of the C2+ product or poor long-term stability. Herein, we report a facile and scalable anodic corrosion method to synthesize oxygen-rich ultrathin CuO nanoplate arrays, which form Cu/Cu2O heterogeneous interfaces through self-evolution during electrocatalysis. The catalyst exhibits a high C2H4 Faradaic efficiency of 84.5%, stable electrolysis for ~55 h in a flow cell using a neutral KCl electrolyte, and a full-cell ethylene energy efficiency of 27.6% at 200 mA cm-2 in a membrane electrode assembly electrolyzer. Mechanism analyses reveal that the stable nanostructures, stable Cu/Cu2O interfaces, and enhanced adsorption of the *OCCOH intermediate preserve selective and prolonged C2H4 production. The robust and scalable produced catalyst coupled with mild electrolytic conditions facilitates the practical application of electrochemical CO2 reduction.

SUBMITTER: Liu W 

PROVIDER: S-EPMC8986799 | biostudies-literature | 2022 Apr

REPOSITORIES: biostudies-literature

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Electrochemical CO<sub>2</sub> reduction to ethylene by ultrathin CuO nanoplate arrays.

Liu Wei W   Zhai Pengbo P   Li Aowen A   Wei Bo B   Si Kunpeng K   Wei Yi Y   Wang Xingguo X   Zhu Guangda G   Chen Qian Q   Gu Xiaokang X   Zhang Ruifeng R   Zhou Wu W   Gong Yongji Y  

Nature communications 20220406 1


Electrochemical reduction of CO<sub>2</sub> to multi-carbon fuels and chemical feedstocks is an appealing approach to mitigate excessive CO<sub>2</sub> emissions. However, the reported catalysts always show either a low Faradaic efficiency of the C<sub>2+</sub> product or poor long-term stability. Herein, we report a facile and scalable anodic corrosion method to synthesize oxygen-rich ultrathin CuO nanoplate arrays, which form Cu/Cu<sub>2</sub>O heterogeneous interfaces through self-evolution d  ...[more]

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