The integration of inorganic and organic semiconductor components in composites has tremendous potential in photocatalysis, owing to the ultrafast photogenerated exciton dissociation and slow carrier recombination kinetics at their interfaces, which can result in enhanced photocatalytic performances. By exploiting the synergy among morphology modulation, sulfur vacancy (Vs) engineering, and close interface control, a novel inorganic–organic Vs-ZnIn2S4/ tetrakis (4-carboxyphenyl) zinc porphyrin (Zn-TCPP) composite for photocatalytic hydrogen evolution (PHE) was successfully synthesized via microwave-assisted solvothermal and self-assembly methods. The cocatalyst-free PHE rate of Vs-ZnIn2S4/Zn-TCPP (ZZT-20 %) reaches 8.997 mmol h−1 g−1 under visible light irradiation, which is 10.9, 2.2, and 67.1 times that of ZnIn2S4, Vs-ZnIn2S4, and Zn-TCPP, respectively. Moreover, the apparent quantum yield of ZZT-20 % under 420 nm monochromatic light (1.11 %) clearly exceeds that of Vs-ZnIn2S4. Testing experiments and DFT calculations revealed that the significantly enhanced PHE activity can be mainly attributed to the Z-scheme charge transfer mechanism, which greatly improves the visible light response range and redox potentials. Remarkably, Vs sites act as electron traps, inducing the vertical transport of electrons within the bulk phase and their accumulation at the surface Zn–S bonds. Simultaneously, van der Waals forces and weak hydrogen bonds between Vs-ZnIn2S4 and the Zn-TCPP interface cause the rapid migration of photogenerated electrons to Zn-TCPP. This work not only reveals new insights into the structure–property relationships of inorganic–organic Vs-ZnIn2S4 and Zn-TCPP composites, but also provides an appropriate strategy for cleaner water resourcelization and sustainable solar energy conversion.
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