Defects Induced in Situ Reconstruction of CdS with Oxygen‐Tolerance Up to 23% in the Photocatalytic CO <sub>2</sub> Reduction

X Xiaoyu Liang (Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering) P Pengcheng Feng (State Key Laboratory of Coal Conversion Institute of Coal Chemistry Chinese Academy of Sciences Taiyuan Shanxi P.O. Box 165 030001 China) X Xinxin Zhang (Center for Ultrafast Science and Technology, State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, Zhang Jiang Institute for Advanced Study) Y Yan Liang (State Key Laboratory of Fine Chemicals, School of Chemistry) M Min Ji M Mei Dong (State Key Laboratory of Coal Conversion) S Shengyang Tao (State Key Laboratory of Fine Chemicals School of Chemistry Dalian University of Technology Dalian Liaoning 116024 China) X Xinkui Wang (State Key Laboratory of Fine Chemicals School of Chemistry Dalian University of Technology Dalian Liaoning China) M Min Wang

Abstract

Abstract Direct driving the photocatalytic reduction of CO 2 from air or flue gas to produce value‐added chemicals and fuels is very challenging due to the suppressing effect of the more favorable thermodynamically oxygen reduction reaction (ORR). Herein, we presented a novel oxygen‐involved reconstruction pathway on a unique defective CdS‐D in the photocatalytic reduction of CO 2 . The material is highly tolerant to O 2 and generates 2766.7 µmol g −1 h −1 of CO under visible light irradiation in the presence of up to 23% content of O 2 . Intriguingly, instead of inhibiting the performance of CO 2 reduction, the presence of oxygen positively promotes it, CO generation rate is up to 5124 µmol g −1 h −1 after multiple experimental cycles. The meticulously structural analysis reveals that the CdS‐D with abundant defects tended to accumulate photogenerated holes, and S 2− is oxidized to SO 4 2− in the presence of oxygen to produce Cd 2 SO 4 (OH) 2 as the active center for preferable CO 2 adsorption and inhibit the O 2 adsorption, which is the root cause for the high tolerance of oxygen in CO 2 reduction (CO 2 RR). This work reveals a unique reconstruction process of sulfides photo corrosion, which provides a new idea for realizing the direct conversion of low‐concentration CO 2 by omitting expensive carbon capture or purification in industrial carbon resource utilization.

Article Details

Volume / Issue Vol. 64, Issue 47
Published November 17, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

X

Xiaoyu Liang

Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering

P

Pengcheng Feng

State Key Laboratory of Coal Conversion Institute of Coal Chemistry Chinese Academy of Sciences Taiyuan Shanxi P.O. Box 165 030001 China

X

Xinxin Zhang

Center for Ultrafast Science and Technology, State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, Zhang Jiang Institute for Advanced Study

Y

Yan Liang

State Key Laboratory of Fine Chemicals, School of Chemistry

M

Min Ji

M

Mei Dong

State Key Laboratory of Coal Conversion

S

Shengyang Tao

State Key Laboratory of Fine Chemicals School of Chemistry Dalian University of Technology Dalian Liaoning 116024 China

X

Xinkui Wang

State Key Laboratory of Fine Chemicals School of Chemistry Dalian University of Technology Dalian Liaoning China

M

Min Wang