摘要
Lattice strain is commonly acknowledged as an effective strategy for tuning the catalytic activity of transition metals, yet its direct impact on Fenton-like reactions remains not fully understood. Herein, we introduce compressive strain into CoMn 2 O 4 via thermal expansion effects in conjunction with a component regulation strategy to enhance peroxymonosulfate (PMS)-based Fenton-like activation. Structural analysis reveals that the compressively strained features enhance metal-oxygen bond coupling and induces the formation of a substantial amount of oxygen vacancies, which promote PMS adsorption and interfacial charge transfer. The obtained CoMn 2 O 4 (2:1)/PMS system demonstrates efficient and stable removal of organic pollutants via dominant nonradical pathways ( 1 O 2 ), and the reaction kinetics was enhanced from 0.078 min −1 to 0.264 min −1 , and the removal rate for sulfadiazine (SD) was as high as 99.8% within 30 min after five cycles. Furthermore, the remarkable feasibility of the CoMn 2 O 4 (2:1)/PMS system for practical wastewater treatment in real river water and pharmaceutical effluents was demonstrated, particularly through the development of a catalytic membrane filtration system and an in-situ floating water treatment device. This study offers new insights into the design of high-performance PMS activation catalysts via lattice strain engineering.
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