Embedding Au Quantum Dots in Rimous Cadmium Sulfide Nanospheres for Enhanced Photocatalytic Hydrogen Evolution

Rational design and development of new‐generation photocatalysts with high hydrogen evolution activity is recognized as an effective strategy to settle energy crisis. To this regard, hybrid photocatalysts of Au quantum dots embedded in rimous cadmium sulfide nanospheres are synthesized by using a si...

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Bibliographic Details
Published in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2016-12, Vol.12 (48), p.6735-6744
Main Authors: Kuang, Pan-Yong, Zheng, Ping-Xuan, Liu, Zhao-Qing, Lei, Jin-Long, Wu, Hao, Li, Nan, Ma, Tian-Yi
Format: Article
Language:English
Subjects:
Cadmium sulfides
charge carriers
Degradation
Gold
Hydrogen evolution
Nanospheres
Nanotechnology
Photocatalysis
Photocatalysts
Quantum dots
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Summary:Rational design and development of new‐generation photocatalysts with high hydrogen evolution activity is recognized as an effective strategy to settle energy crisis. To this regard, hybrid photocatalysts of Au quantum dots embedded in rimous cadmium sulfide nanospheres are synthesized by using a simple hydrothermal process followed by photoreduction. The rimous cadmium sulfide nanospheres with rough surface and irregular fissures greatly strengthen their adhesion and interaction with Au quantum dots, which effectively facilitates the separation, restrains the recombination, and accelerates the consumption of photoinduced electron‐hole pairs. Impressively, the highest photocatalytic activity for hydrogen generation (601.2 μmol h−1 g−1) and organic pollutant degradation (100% degradation in 80 min) is obtained by adjusting the Au mass loading to achieve uniform distribution. This work paves new way to the exploitation of highly efficient metal/semiconductor hybrid photocatalysts for clean energy generation and environment restoration. A novel family of hybrid photocatalysts composed of gold quantum dots embedded in rimous cadmium sulfide nanospheres is developed through a facile hydrothermal process followed by photoreduction. The robust host‐guest interaction, favorable charge separation, and accelerated electron‐hole pairs' consumption together lead to outstanding photocatalytic hydrogen evolution and dye degradation performance, highly potential for clean energy generation and environment restoration.
ISSN:1613-6810
1613-6829
DOI:10.1002/smll.201602870