摘要
ABSTRACT Photocatalytic water splitting to produce H 2 using semiconductor photocatalysts is a reliable approach to alleviating energy shortages and environmental pollution. However, the inadequate light-harvesting ability, rapid photogenerated carrier recombination, and inferior redox capacity of the individual photocatalysts restrict their photocatalytic activity . To address these limitations, a hierarchical S-scheme heterojunction of ZnIn 2 S 4 -nanosheet-decorated flower-like TiO 2 microspheres for enhancing photocatalytic H 2 evolution, purposely constructed through in situ chemical bath deposition, has been reported. The as-synthesized TiO 2 /ZnIn 2 S 4 heterojunctions exhibited ZnIn 2 S 4 -content-dependent photocatalytic activity for solar-driven H 2 evolution. As a result, the optimized TiO 2 /ZnIn 2 S 4 heterojunction exhibited a superior photocatalytic H 2 evolution rate of 6.85 mmol g –1 h –1 , approximately 171.2- and 3.9-fold with respect to that obtained on pure TiO 2 and ZnIn 2 S 4 , respectively, mainly attributed to the unique hierarchical structure, extended light-harvesting ability, enhanced redox capacity, and improved separation and transfer efficiencies of the photogenerated carriers induced by the S-scheme heterojunctions. Simultaneously, a detailed analysis of the S-scheme electron transfer pathway in the TiO 2 /ZnIn 2 S 4 heterojunction was performed using in situ irradiated X-ray photoelectron spectroscopy and electron paramagnetic resonance spectroscopy . This study provides insights into the design of highly active heterojunction photocatalysts for sustainable solar-to-fuel energy conversion.
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