摘要
While photocatalytic oxidation of 5-hydroxymethylfurfural (HMF) into valuable chemicals represents a crucial strategy for advancing carbon neutrality, low conversion rates and poor product selectivity hinder commercialization. In this study, a dual-sulfur-vacancy (S v )-mediated Cu 2 ZnSnS 4− x /ZnIn 2 S 4− x all-multinary-sulfide p-n heterojunction was designed for high-efficiency photocatalysis. Specifically, S v introduction significantly enhanced light absorption, photothermal properties, and interfacial electric fields (IEF). Consequently, the Cu 2 ZnSnS 4− x /ZnIn 2 S 4− x heterostructure achieved outstanding photothermal-assisted photocatalytic oxidation of HMF to 2,5-diformylfuran (DFF), with an oxidation rate of 94.1%, which was 9.1 and 4.0 times higher than that of Cu 2 ZnSnS 4 and ZnIn 2 S 4 , respectively. The selectivity of DFF reached 92.8%. Additionally, mechanistic analysis identified primary active species and possible reaction pathways. This study provides a potential strategy for the design of photocatalytic systems for efficient HMF oxidation.
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