摘要
Comprehending the catalytic reaction implementation for heterostructure photocatalysts is crucial by scrutinizing the spatial separation and transfer process of photoexcited charges at nanoscale junctions. Herein, we fabricated the F-doped TiO 2 /ZnIn 2 S 4 -based S-scheme heterostructure using a direct liquid-assembly method. The optimum hydrogen evolution rate (HER) of ∼ 1.58 mmol g –1 h –1 was acquired for 30-F 3 T@ZIS, which was about 15 and 2 times superior to the pristine F-doped TiO 2 and ZnIn 2 S 4 , respectively. The interaction between F-doped TiO 2 and ZnIn 2 S 4 facilitated the charge transfer from ZIS to F 3 T which was confirmed through XPS. UV–vis spectroscopy and Mott–Schottky validated that F-doped TiO 2 and ZnIn 2 S 4 retain the suitable energy band alignment for the S-scheme heterostructure. In situ, KPFM and EPR analysis revealed that F-doped TiO 2 and ZnIn 2 S 4 possess a spontaneous photoelectrochemical response, and their junction significantly improves the internal electric field by separating photoexcited charge carriers. This work provides a conclusive experimental and theoretical validation for an internal electric field and charge flow direction in non-noble-metal-based heterostructure photocatalysts.
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