Amorphization Strategy to Circumvent the Oxo Wall for Generating Active Co(IV)═O Species in Fenton‐Like Reactions
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
Authors (11)
Peigen Liu
National Synchrotron Radiation Laboratory
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
Shaokang Yang
Zixiang Huang
National Synchrotron Radiation Laboratory (NSRL)
Yu Bai
Qichen Liu
Rongao Zhang
National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei Anhui 230029 P.R. China
Hongliang Li
Hefei National Research Center for Physical Sciences at the Microscale
Xun Hong
Hefei National Research Center for Physical Sciences at the Microscale, Department of Applied Chemistry
Dingsheng Wang
Department of Chemistry
Xusheng Zheng
National Synchrotron Radiation Laboratory