Amorphization Strategy to Circumvent the Oxo Wall for Generating Active Co(IV)═O Species in Fenton‐Like Reactions

P Peigen Liu (National Synchrotron Radiation Laboratory) J Junsheng Song (CAS Key Laboratory of Urban Pollutant Conversion Department of Environmental Science and Engineering University of Science and Technology of China Hefei Anhui 230026 P.R. China) S Shaokang Yang Z Zixiang Huang (National Synchrotron Radiation Laboratory (NSRL)) Y Yu Bai Q Qichen Liu R Rongao Zhang (National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei Anhui 230029 P.R. China) H Hongliang Li (Hefei National Research Center for Physical Sciences at the Microscale) X Xun Hong (Hefei National Research Center for Physical Sciences at the Microscale, Department of Applied Chemistry) D Dingsheng Wang (Department of Chemistry) X Xusheng Zheng (National Synchrotron Radiation Laboratory)

Abstract

Abstract High‐valent Co(IV)═O species have garnered significant attention as a promising non‐radical reactive species. However, their selective generation encounters substantial challenges due to the oxo wall rule that emphasizes intrinsic instability of the terminal metal–oxygen (M─O) bond. Here, we propose an amorphization strategy for TiO 2 support to circumvent the limitation of oxo wall, favoring the formation of high‐valent Co(IV)═O species. The advantages of Co(IV)═O species in terms of oxidative activity, durability, and environmental tolerance were investigated by Fenton‐like catalysis. Mechanistic studies revealed that amorphous TiO 2 endowed Co single atoms with a Co‐O 4 tetrahedral structure and a high‐spin state of 3 d electron, leading to strong Co 3 d ‐O 2 p interactions that promote peroxymonosulfate (PMS) activation. Notably, the produced Co(IV)═O species adopted a trigonal‐bipyramidal‐like configuration, which mitigated the electron occupation in the antibonding orbitals of terminal M─O bond, thus bypassing the oxo wall. This work enhances the understanding of the mechanism underlying heterogeneous Co(IV)═O formation and broadens strategies for preparing efficient catalysts for critical oxidation reactions.

Article Details

Volume / Issue Vol. 65, Issue 6
Published February 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

P

Peigen Liu

National Synchrotron Radiation Laboratory

J

Junsheng Song

CAS Key Laboratory of Urban Pollutant Conversion Department of Environmental Science and Engineering University of Science and Technology of China Hefei Anhui 230026 P.R. China

S

Shaokang Yang

Z

Zixiang Huang

National Synchrotron Radiation Laboratory (NSRL)

Y

Yu Bai

Q

Qichen Liu

R

Rongao Zhang

National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei Anhui 230029 P.R. China

H

Hongliang Li

Hefei National Research Center for Physical Sciences at the Microscale

X

Xun Hong

Hefei National Research Center for Physical Sciences at the Microscale, Department of Applied Chemistry

D

Dingsheng Wang

Department of Chemistry

X

Xusheng Zheng

National Synchrotron Radiation Laboratory