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Optimizing C─C Coupling on Cu0/Cu+/Ga Interfaces by Enhancing Active Hydrogen Absorption for Excellent CO2-to-C2+ Electrosynthesis

  • Xiaoshuang Qi
  • , Yikai Yang
  • , Yupeng Lan
  • , Xiuming Bu*
  • , Siwei Yang
  • , Di Yin
  • , Hongwen Huang*
  • , Johnny C. Ho*
  • , Xianying Wang*
  • *Corresponding author for this work
  • Hunan University
  • CAS - Shanghai Institute of Ceramics
  • CAS - Shanghai Institute of Microsystem and Information Technology
  • City University of Hong Kong

Research output: Contribution to journalArticlepeer-review

Abstract

The electrocatalytic reduction of CO2 (CO2RR) to high-value chemicals and fuels offers a promising route for a clean carbon cycle. However, it often suffers from low catalytic activity and poor selectivity. Heterostructure construction has been shown to be an effective strategy for producing multi-carbon products, but the synergistic mechanisms between multiple active sites resulting from the reconstruction process remain unclear. In this study, a Ga2O3/CuO heterostructure is established via a simple sol–gel method to produce C2+ products. Experimental results demonstrate that Ga2O3 stabilizes Cu+ to form Cu0/Cu+/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C─C coupling reaction pathway from *OCCO to the asymmetric *OCCHO coupling path with a lower energy barrier. As a result, the catalysts exhibit superior CO2RR performance, achieving a 70.1% C2+ Faradaic efficiency at −1.2 VRHE in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.

Original languageEnglish
Article number2500538
JournalSmall
Volume21
Issue number15
DOIs
StatePublished - 16 Apr 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Cu/Cu
  • asymmetric coupling
  • electrocatalytic CO reduction
  • ethylene

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