Regulating the properties of heterogeneous catalyst for efficient peroxymonosulfate (PMS) activation to pollutants degradation remains a challenge in photo-assisted Fenton-like reaction (PF) system. In this study, the novel S-scheme MoSe2/Fe2O3 (H-FMS) heterojunction with hollow nanostructure was successfully developed as visible-light-driven PMS activator for removal of ciprofloxacin (CIP). The prepared H-FMS catalyst in PMS/H-FMS/light system exhibits outstanding photocatalytic performance for CIP degradation, achieving 95.92 % removal of 5 mg/L CIP in 30 min with 0.5 mM PMS. The construction of S-scheme heterojunction provides photoinduced carriers with longer lifetime and higher redox abilities, thus sufficient photogenerated carriers are supplied to directly activate PMS. Simultaneously, the hollow nanostructure possessing multiple light reflection and scattering behaviors further facilitates the utilization of visible light. More importantly, high concentration of photoinduced electrons with high reduction ability in MoSe2 is conducive to continuous exposure of Mo4+ active sites for PMS activation through cycling between transition metal valence states. Overall, effectively separated electron-hole pairs and continuously exposed transition metal active sites both contribute to efficient activation of PMS as well as multi-path generation of ROS, leading to significant improvement in CIP degradation. The results of quenching experiment, electron spin resonance (ESR) technology, liquid chromatography-mass spectrometry (LC-MS) and density functional theory (DFT) calculation confirm that both free radicals (SO4∙-, •OH and O2∙-) and non radicals (1O2 and h+) attack the active sites of CIP possessing high Fukui index, thus contributing to CIP degradation. This work would provide a novel insight for future development and application of photocatalytic PMS activation catalysts in water remediation.
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