摘要
Reactive oxygen species (ROS)-mediated sterilization typically relies on continuous light irradiation or exogenous H 2 O 2 addition, limiting their practical utility under dark or resource-limited conditions. Herein, we rationally design an S-scheme MIL-100(Fe)/Zn 3 In 2 S 6 heterojunction (M 5 Z 1 –1@ZIS2) by in-situ growing Zn-doped MIL-100(Fe) on Zn 3 In 2 S 6 , achieving synergistic light-harvesting and ROS self-supply capabilities. The incorporation of Zn 3 In 2 S 6 enhances electron density around Fe 2+ sites while modulating Fe 3+ states, significantly improving O₂ activation and H 2 O 2 affinity. This unique electronic regulation enables the heterojunction to generate superoxide radical(·O₂ − )-dominated ROS even in the dark. Notably, visible-light pretreatment induces active In sites in Zn 3 In 2 S 6 to produce H 2 O 2 , which accumulates and sustains the FeII/FeIII redox cycle in the absence of light, driving continuous hydroxyl radical(·OH)-dominated ROS generation. Combined characterizations including X-ray photoelectron spectroscopy (XPS) and Electron Paramagnetic Resonance (EPR) confirm H₂O₂-mediated Fe 2+ regeneration and ROS persistence. The M 5 Z 1 –1@ZIS2 heterojunction exhibits exceptional antibacterial performance, achieving ≥99.9% inactivation of Escherichia coli ( E. coli ) within 1.5 h in the dark and 40 min under visible light. This work provides a strategy for designing self-sustaining catalytic systems that leverage light-driven H₂O₂ supply to enable day-night ROS functionality. Furthermore, M 5 Z 1 –1@ZIS2 loaded on polyvinylidene fluoride (PVDF) film can achieve an efficiency of over 99% for particulate matter (PM) pollutants at the wind speeds of 1.5 m/s and 0.5 m/s and reach a maximum adsorption efficiency of 99.5% for formaldehyde within 19 min, highlighting its potential for all-weather air purification via ROS-mediated environmental remediation.
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