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

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 optoel...

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Detalles Bibliográficos
Autores principales: Vamvasakis, Ioannis, Andreou, Evangelos K., Armatas, Gerasimos S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10490144/
https://www.ncbi.nlm.nih.gov/pubmed/37686934
http://dx.doi.org/10.3390/nano13172426
Descripción
Sumario: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 ~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 (~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.