Applied Catalysis2022,Vol.30512.DOI:10.1016/j.apcatb.2022.121082

Anode-cathode interchangeable strategy for in situ reviving electrocatalysts’ critical active sites for highly stable methanol upgrading and hydrogen evolution reactions

Zhao B. Liu J. Wang L. Luo J.-L. Fu X.-Z. Xu C. Shakouri M. Feng R. Zhang Y. Zhang J.
Applied Catalysis2022,Vol.30512.DOI:10.1016/j.apcatb.2022.121082

Anode-cathode interchangeable strategy for in situ reviving electrocatalysts’ critical active sites for highly stable methanol upgrading and hydrogen evolution reactions

Zhao B. 1Liu J. 1Wang L. 1Luo J.-L. 1Fu X.-Z. 1Xu C. 2Shakouri M. 3Feng R. 3Zhang Y. 4Zhang J.5
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作者信息

  • 1. Shenzhen Key Laboratory of Polymer Science and Technology Guangdong Research Center for Interfacial Engineering of Functional Materials College of Materials Science and Engineering Shenzhen University Shenzhen
  • 2. Department of Chemical and Materials Engineering University of Alberta
  • 3. Canadian Light Source Inc.
  • 4. Instrumental Analysis Center of Shenzhen University(Lihu Campus) Shenzhen University
  • 5. Institute for Sustainable Energy College of Sciences Shanghai University
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Abstract

? 2022 Elsevier B.V.Surface re-construction was a common phenomenon for non-oxide compound electrocatalysts in anodic oxidation reaction in alkaline electrolyte but surface deactivation arising from excessive oxidation/hydroxylation was critical hindrance to the long-term stability. Herein, a unique anode-cathode interchangeable electrocatalysis strategy is proposed for methanol upgrading reaction (MUR) and hydrogen co-generation in membrane-free electrolyzer. A periodical electrolysis is taken place for the Ni3S2/CNTs electrode at positive/negative currents over time. Compared with the traditional chronopotentiometry mode, the MUR-HER coupled reactions by periodically switching anode/cathode per hour present an excellent long-term stability at high current densities of ± 100 mA cm?2, in which the Faradaic efficiencies for both H2 and value-added formate are greater than 95%. Substantial experimental results and deep theoretical DFT studies signify that the successful application of this strategy is mainly due to the reversible modulation of oxidation/hydroxylation status on Ni3S2 surface, which effectively prevent the surface active structures of electrocatalysts from over-oxidation.

Key words

Active sites recovery/Anode-cathode exchange/Hydrogen generation/Nickel sulfide/Stable electrocatalysis

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出版年

2022
Applied Catalysis

Applied Catalysis

ISSN:0926-3373
被引量17
参考文献量53
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