In‐Situ Probing CO Activation in Sulfur‐Enhanced Paired Electrocatalysis for CO <sub>2</sub> ‐to‐C <sub>2+</sub> Conversion with Alcohol Oxidation

F Feng Ming Yap (School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia) S Shaoyu Yuan (College of Energy State Key Laboratory of Physical Chemistry of Solid Surfaces Xiamen University Xiamen 361102 China) J Jian Yiing Loh (School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia) J Jingjuan Wang (New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering) X Xianhai Zeng (College of Energy State Key Laboratory of Physical Chemistry of Solid Surfaces Xiamen University Xiamen 361102 China) W Wee‐Jun Ong (School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia)

Abstract

Abstract In a world striving for sustainable energy, advanced electrocatalysts are pivotal to enabling efficient chemical transformations with minimal energy costs. Herein, we uncover a practical approach for the simultaneous electrochemical CO 2 reduction (CO 2 RR) and alcohol oxidation (AOR), enabling the selective valuable chemicals production. Central to this innovation is a self‐supported electrocatalyst, featuring sulfur‐enhanced CuBi 2 O 4 nanospheres anchored on NrGO nanosheets (SCB/NG), achieved a faradaic efficiency for C 2+ products (FE C2+ ) exceeding 92.4% over 200 h, while demonstrating near‐total selectivity for benzaldehyde and &gt;83% for furfural. Beyond that, in situ Raman spectroscopy and DFT calculations reveal *CO dimerization and the key intermediates coverage, providing deep mechanistic insights into the reaction pathway. Additionally, by being integrated into a solar‐powered platform, the bifunctional system achieves a solar‐to‐fuel conversion efficiency of 16% with over 98% retention, offering a scalable strategy for coupling CO 2 utilization with high‐value chemical production and paving the way toward energy‐efficient, carbon‐neutral technologies.

Article Details

Volume / Issue Vol. 64, Issue 48
Published November 24, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

F

Feng Ming Yap

School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia

S

Shaoyu Yuan

College of Energy State Key Laboratory of Physical Chemistry of Solid Surfaces Xiamen University Xiamen 361102 China

J

Jian Yiing Loh

School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia

J

Jingjuan Wang

New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering

X

Xianhai Zeng

College of Energy State Key Laboratory of Physical Chemistry of Solid Surfaces Xiamen University Xiamen 361102 China

W

Wee‐Jun Ong

School of Energy and Chemical Engineering Xiamen University Malaysia Selangor Darul Ehsan 43900 Malaysia