摘要
In this work, S-scheme Ti-MOF/Cs 2 AgBiBr 6 heterojunction photocatalysts were developed via an in situ self-assembly strategy, achieving satisfactory interfacial contact, matched band alignment, enhanced charge separation, and redox activity. The optimized Ti-MOF/Cs 2 AgBiBr 6 composite exhibited remarkable photocatalytic performance toward benzyl alcohol oxidation under visible light, achieving > 99 % conversion and selectivity without external oxidants and sacrificial agents. It represents a fourfold enhancement over individual components, while maintaining broad substrate applicability and excellent cycling stability. The S-scheme configuration ensures sufficient oxidation potential compared with conventional Type-II systems. This work addresses challenges of limited bandgap tunability and inefficient carrier transport in selective aromatic alcohol oxidation, establishing a promising strategy for designing efficient lead-free perovskite photocatalysts toward sustainable organic transformations.
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