Photocatalytic technology holds significant importance and feasibility in bacterial inactivation and antibiotic degradation. This study successfully fabricated a hierarchical inorganic BiOCl0.7I0.3-P/TiO2 (BOCI-P/TH) S-scheme heterojunction by in-situ growth of BiOCl0.7I0.3-P (BOCI-P) nanosheets on TiO2 hollow spheres (TH), which was capable of suppressing charge carrier recombination and enhancing oxidative-reductive capability. The charge transfer mechanism of the hierarchical BOCI-P/TH composite was elucidated by radical-trapping electron paramagnetic resonance and X-ray photoelectron spectroscopy analysis, revealing the mechanism behind high activities of the BOCI-P/TH photocatalysts in antibacterial and degradation. It was found that the multiple light-scattering in hierarchical structure enhanced the light absorption, tight contacted interface decreased electron transfer distance, and S-scheme charge transfer inhibited charge recombination. As a result, electrons and holes with strong redox ability were generated, resulting the formation of abundant ·O2- and ·OH radicals, achieving efficient sterilization and antibiotic degradation. The BOCI-P/TH catalysts exhibited outstanding photocatalytic activity and photostability for deactivating Staphylococcus aureus (99.99%) and degrading Rhodamine B (99.98%), tetracycline hydrochloride (84.81%), and ofloxacin (99.95%). This research provided valuable insights into the multi-strategy design of photocatalysts and the application of dual-functional catalysts in various environments.
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