In Situ DXAFS Reveals Active Cu δ+ Intermediates of F-CuO Enhancing CO 2 -to-C 2+ Electrocatalysis
Year: 2026
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Electrochemical CO 2 reduction reaction (CO 2 RR) represents a promising strategy for converting CO 2 into value-added chemicals and fuels, contributing to carbon neutrality. Copper (Cu)-based catalysts hold particular promise in this field due to their capability of producing multicarbon (C 2+ ) products. However, copper-based catalysts still suffer from structural instability and unclear dynamic evolution under operating conditions. This study elucidates the crucial role of fluorine (F) doping in enhancing the structural stability of copper oxide (CuO) during the electrocatalytic CO 2 RR. Using in situ dispersive X-ray absorption fine structure (DXAFS) coupled with unsupervised machine learning analysis, we directly observed the formation and stabilization of a Cu δ + intermediate phase (0 < δ < 2) in the F-CuO catalyst under applied potential. In contrast, undoped CuO underwent a rapid and direct transformation to metallic Cu 0 under identical conditions, with no detectable intermediate state. This study establishes anionic doping as an effective strategy to modulate the electronic structure of copper catalysts, thereby stabilizing critical reaction intermediates and enabling highly efficient and stable CO 2 -to-C 2+ conversion.
Source: Photon Science
Authors: Longfei Hu, Tiantian Li, Dan Wu, Hui Huang, Yuanhua Sun, Mengyuan Liu, Airong Xu, Qiquan Luo, Tao Ding, Xiaokang Liu, Tao Yao
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid:
Funders: Salt Science Research Foundation, National Natural Science Foundation of China, Chinese Academy of Sciences, China Postdoctoral Science Foundation, Youth Innovation Promotion Association of the Chinese Academy of Sciences, University of Science and Technology of China, National Synchrotron Radiation Laboratory, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Youth Innovation Promotion Association
OpenAlex ID: W7128928740
