Photo‐Self‐Fenton Reaction Mediated by Silver Single Atom and Cluster Photocatalysts for Highly Selective Generation of Singlet Oxygen Toward Efficient Organic Wastewater Treatment

D Di Luo (Institute of Photochemistry and Photofunctional Materials) H Han Xiao (Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States) Y Yupeng Yang J Jiaxing Li (Institute of Photochemistry and Photofunctional Materials) Y Yixing Wang X Xiaoru Huang (Institute of Photochemistry and Photofunctional Materials) M Mixuan Zhang (Institute of Photochemistry and Photofunctional Materials) L Lihui Wang (Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University) J Jiarui Yang (Department of Chemistry) J Jiangzhi Zi (Institute of Photochemistry and Photofunctional Materials) Z Zichao Lian (Institute of Photochemistry and Photofunctional Materials) G Guisheng Li (School of Materials and Chemistry) H Hexing Li (Chinese Education Ministry Key Lab and Joint International Research Lab of Resource Chemistry, Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science)

Abstract

AbstractThe persistent organic pollutants in wastewater have caused a heavy threat to ecosystems and humans, but selective removal of these pollutants still faces challenges due to low efficiency, extra addition of oxidation agents, and many highly toxic intermediate products. Herein, we report an efficient, fast kinetic conversion via a photo‐self‐Fenton‐like system of *OOH intermediate‐involved oxidation pathway with a high selection generation of singlet oxygen (1O2) from the novel in situ H2O2 heterolytic activation route for the first time. The single‐atom and cluster‐doped zinc oxide (AgSA–AgC/ZnO) was successfully synthesized to achieve the 100% degradation yield and 80% total of carbon (TOC) of the p‐chlorophenol (4‐CP) as the typical pollutant under solar‐light irradiation and exhibit long‐term activity in a self‐designed photo‐Filter reactor for 4‐CP degradation. It was attributed to the accelerated cycles from Aghighδ+ site to Aglowδ+ site in Fenton‐like catalysis, achieving the rapid selection conversion from the H2O2 heterolytic cleavage to ∼100% 1O2 via the intermediate *OOH at the Ag SA sites for ring‐opening reaction and reactive H* at the Ag clusters sites for dechlorination reaction, respectively. This discovery gives the deep understanding of the high‐performance photo‐self‐Fenton reaction through in situ cycles of variable metals for the organic contaminants treatment.

Article Details

Volume / Issue Vol. 64, Issue 23
Published June 02, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

D

Di Luo

Institute of Photochemistry and Photofunctional Materials

H

Han Xiao

Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States

Y

Yupeng Yang

J

Jiaxing Li

Institute of Photochemistry and Photofunctional Materials

Y

Yixing Wang

X

Xiaoru Huang

Institute of Photochemistry and Photofunctional Materials

M

Mixuan Zhang

Institute of Photochemistry and Photofunctional Materials

L

Lihui Wang

Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University

J

Jiarui Yang

Department of Chemistry

J

Jiangzhi Zi

Institute of Photochemistry and Photofunctional Materials

Z

Zichao Lian

Institute of Photochemistry and Photofunctional Materials

G

Guisheng Li

School of Materials and Chemistry

H

Hexing Li

Chinese Education Ministry Key Lab and Joint International Research Lab of Resource Chemistry, Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science