4.7 Article

Hierarchical hollow-microsphere cadmium sulfide-carbon dots composites with enhancing charge transfer efficiency for photocatalytic CO2 reduction

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 936, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.168286

Keywords

CdS; Carbon dots; Hierarchical Hollow-Microsphere; Photocatalytic CO 2 reduction

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A novel carbon dots modified CdS hollow sphere (CDs/CdS) has been successfully synthesized, exhibiting significantly improved solar-driven CO2 reduction performance. The formed hollow sphere and seamless contact contribute to the excellent performance and stability, while CDs as cocatalyst boost the charge separation and stabilize the electrons. This study provides a feasible perspective for designing and fabricating high-efficient catalysts for CO2 photoreduction.
Construction of hierarchical heterostructure is considered as a promising approach to promote photo -catalytic CO2 reduction, yet the report about CdS semiconductor for photocatalytic activity is still restricted caused by its rapid charge recombination. Herein, a novel carbon dots (CDs) modified CdS hollow sphere (CDs/CdS) has been successfully synthesized by multi-step including template-assembly, template-removal, and ultrasonic impregnation processes. This noble-metal-free heterostructure exhibits significantly im-proved solar-driven CO2 reduction performance, and the optimal CDs/CdS presents CO yield rate of 16.09 mu mol g-1 h-1, which is nearly 4 times higher than that of pristine CdS hollow sphere under the same condition. The excellent performance and stability of CDs/CdS are due to the formed hollow sphere and seamless contact, which can possess large inner space, intimate interfacial contact for charge transport and improve concentration of sacrificial agent. Meanwhile, CDs as cocatalyst can boost the charge separation and stabilize the electrons. This study can afford a feasible perspective to design and fabricate high-efficient catalyst for CO2 photoreduction. (c) 2022 Elsevier B.V. All rights reserved.

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