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Regulating facet exposure and sulfur vacancy in magnetic greigite nanosheet for boosting heterogeneous Fenton-like reaction towards efficient degradation of metronidazole under visible light irradiation:Synergistic enhancement effect,DFT calculations and mechanism insight

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摘要 Environmentally friendly iron catalysts have attracted widespread attention in the heterogeneous Fenton-like reaction based on peroxymonosulfate(PMS)for the degradation of emerging pollutants in water,while it has always suffered from the disadvantage of low catalytic activity.Herein,we successfully pre-pared the magnetic greigite(Fe3 S4)nanosheet with the exposed{011}facet and rich sulfur vacancies(FS-1)through a simple solvothermal method.The degradation rate of metronidazole by the FS-1 acti-vating PMS under visible light irradiation was 2.93,and 4.48 more than those of the Fe3 S4 nanosheet with the exposed{011}facet and poor sulfur vacancies,and Fe3 S4 nanobulk with the exposed{112}facet,respectively.The result of electrochemical analysis and theoretical calculation indicated that the exposed{011}facet of prepared FS-1 offered more active sites to adsorb PMS,and the rich sulfur va-cancies on the surface accelerated the electron transfer between oxidants and catalyst.This collaborative effect significantly lowered the energy barrier associated with PMS activation,leading to an increased generation of singlet oxygen.Additionally,the degradation mechanism and pathway of metronidazole,including hydroxyethyl cracking,denitrification,and hydroxylation,were explored in detail through theoretical calculations and high-performance liquid chromatography-mass spectrometry,respectively.This work offers insight into boosting the catalytic performance of environmentally friendly iron-based catalysts.
出处 《Journal of Materials Science & Technology》 2025年第13期27-37,共11页 材料科学技术(英文版)
基金 supported by the National Natural Science Foun-dation of China(NSFC No.22176151) the Wuhan University of Technology Independent Innovation Research Fund Graduate Free Exploration Project(No.104972024JYS0005).
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