4.6 Article

Solid-liquid phase transition induced electrocatalytic switching from hydrogen evolution to highly selective CO2 reduction

Journal

NATURE CATALYSIS
Volume 4, Issue 3, Pages 202-211

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41929-021-00576-3

Keywords

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Funding

  1. National Basic Research Program of China [2017YFA0206702]
  2. Natural Science Foundation of China [21925110, 21890751, 91745113, U1832168, 21701164]
  3. National Program for Support of Top-Notch Young Professionals
  4. Fundamental Research Funds for the Central Universities [WK 2060190084]
  5. Anhui Provincial Natural Science Foundation [1808085MB26]
  6. Chinese Academy of Sciences [XDB36000000, XDB22040402]
  7. China Postdoctoral Science Foundation [2018M642523]
  8. National Natural Science Foundation of China [11525211]

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This study found that solid-liquid phase transition of Ga-Sn/Ga-In alloys can lead to instantaneous and drastic changes in their atomic and electronic structures during electrocatalysis, significantly impacting their catalytic properties.
Conventional strategies for modifying electrocatalysts for efficient CO2 reduction are mainly based on doping, defect/morphology engineering, substrate design and so on. In most cases, these methods can only tune their structures, electronic states and thereby catalytic properties in a gradual way. Here we report that the solid-liquid phase transition of Ga-Sn/Ga-In alloys can induce an instant and radical transformation of their atomic and electronic structures during electrocatalysis, which dramatically impacts their catalytic properties. The transition of Sn/In active components from phase-segregated clusters to dispersed single atoms during melting results in a unique electronic structure through further reduction of both metallic Sn/In and Ga. Such atomic/electronic structure transitions can correlate well with suppression of the hydrogen evolution reaction and an enhanced formate Faradaic efficiency from <35% to >95%. This two-state switching strategy may be extended to other catalytic reactions to determine correlations between their structures and catalytic properties.

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