4.7 Article

Mesoporous Dual-Semiconductor ZnS/CdS Nanocomposites as Efficient Visible Light Photocatalysts for Hydrogen Generation

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NANOMATERIALS
卷 13, 期 17, 页码 -

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MDPI
DOI: 10.3390/nano13172426

关键词

cadmium sulfide; zinc sulfide; metal chalcogenides; nanoparticles; mesoporous materials; nanocomposites; ZnS/CdS heterojunctions; water splitting; photocatalytic hydrogen production

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This study develops a highly efficient visible light photocatalyst for hydrogen generation via water splitting by synthesizing dual-semiconductor nanocomposites. The material exhibits a unique microstructure and good stability, enabling efficient hydrogen production through effective charge transfer and photocatalytic reactions.
The development of functional catalysts for the photogeneration of hydrogen (H-2) via water-splitting is crucial in the pursuit of sustainable energy solutions. To that end, metal-sulfide semiconductors, such as CdS and ZnS, can play a significant role in the process due to their interesting optoelectronic and catalytic properties. However, inefficient charge-carrier dissociation and poor photochemical stability remain significant limitations to photocatalytic efficiency. Herein, dual-semiconductor nanocomposites of ZnS/CdS nanocrystal assemblies (NCAs) are developed as efficient visible light photocatalysts for H-2 generation. The resultant materials, synthesized via a polymer-templated self-polymerization method, comprise a unique combination of similar to 5-7 nm-sized metal-sulfide nanoparticles that are interlinked to form a 3D open-pore structure with large internal surface area (up to 285 m(2) g(-1)) and uniform pores (circa 6-7 nm). By adjusting the ratio of constituent nanoparticles, the optimized ZnS/CdS catalyst with 50 wt.% ZnS content demonstrates a remarkable stability and visible light H-2-evolution activity (similar to 29 mmol g(-1) h(-1) mass activity) with an apparent quantum yield (AQY) of 60% at 420 nm. Photocatalytic evaluation experiments combined with electrochemical and spectroscopic studies suggest that the superior photocatalytic performance of these materials stems from the accessible 3D open-pore structure and the efficient defect-mediated charge transfer mechanism at the ZnS/CdS nanointerfaces. Overall, this work provides a new perspective for designing functional and stable photocatalytic materials for sustainable H-2 production.

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