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[Display omitted] As a renewable green energy, hydrogen has received widespread attention due to its huge potential in solving energy shortages and environment pollution. In this paper, a one-step solvothermal method was applied to grow ultra-thin g-C 3 N 4 (UCN) nanosheets and NiS nanoparticles on the surface of ZnIn 2 S 4 (ZIS). A ternary NiS/ZnIn 2 S 4 /ultra-thin-g-C 3 N 4 composite material with dual high-speed charge transfer channels was constructed for the advancement of the photocatalytic H 2 generation. The optimal ternary catalyst 1.5wt.%NiS/ZnIn 2 S 4 /ultra-thin-g-C 3 N 4 (NiS/ZIS/UCN) achieved a H 2 evolution yield reached to 5.02 mmolg−1h−1, which was 5.23 times superior than that of pristine ZnIn 2 S 4 (0.96 mmolg−1h−1) and even outperform than that of the best precious metal modified 3.0 wt%Pt/ZnIn 2 S 4 (4.08 mmolg−1h−1). The AQY at 420 nm could be achieved as high as 30.5%. The increased photocatalytic performance of NiS/ZIS/UCN could be ascribed to the type-I heterojunctions between intimated ZIS and UCN. In addition, NiS co-catalyst with large quantity of H 2 evolution sites, could result in efficient photo-induced charges separation and migration. Furthermore, the NiS/ZIS/UCN composite exhibited excellent H 2 evolution stability and recyclability. This work would also offer a reference for the design and synthesis of ternary co-catalyst with heterojunction composite for green energy conversion. [ABSTRACT FROM AUTHOR]

The ZnIn 2 S 4 @CdS photocatalyst with tuned catalytic sites promotes selective benzyl alcohol oxidation on the ZnIn 2 S 4 surface and H 2 evolution on the CdS surface. [Display omitted] Photocatalytic selective oxidation of alcohols into aldehydes and H 2 is a green strategy for obtaining both value-added chemicals and clean energy. Herein, a dual-purpose ZnIn 2 S 4 @CdS photocatalyst was designed and constructed for efficient catalyzing benzyl alcohol (BA) into benzaldehyde (BAD) with coupled H 2 evolution. To address the deep-rooted problems of pure CdS, such as high recombination of photogenerated carriers and severe photo-corrosion, while also preserving its superiority in H 2 production, ZnIn 2 S 4 with a suitable band structure and adequate oxidizing capability was chosen to match CdS by constructing a coupled reaction. As designed, the photoexcited holes (electrons) in the CdS (ZnIn 2 S 4) were spatially separated and transferred to the ZnIn 2 S 4 (CdS) by electrostatic pull from the built-in electric field, leading to expected BAD production (12.1 mmol g−1 h−1) at the ZnIn 2 S 4 site and H 2 generation (12.2 mmol g−1 h−1) at the CdS site. This composite photocatalyst also exhibited high photostability due to the reasonable hole transfer from CdS to ZnIn 2 S 4. The experimental results suggest that the photocatalytic transform of BA into BAD on ZnIn 2 S 4 @CdS is via a carbon-centered radical mechanism. This work may extend the design of advanced photocatalysts for more chemicals by replacing H 2 evolution with N 2 fixation or CO 2 reduction in the coupled reactions. [ABSTRACT FROM AUTHOR]