Immobilizing CdS quantum dots and dendritic Pt nanocrystals on thiolated graphene nanosheets toward highly efficient photocatalytic H2 evolution

• DOI: 10.1039/c3nr03043a
• Publication Date: 2013-08-01T14:06:18Z
• Authors: Zheng Fang; Yabo Wang; Jibin Song; Yimin Sun; Jiajing Zhou; Rong Xu; Hongwei Duan
• Keywords: Light; 02 engineering and technology; Sulfides; Catalysis; Nanostructures; Quantum Dots; Cadmium Compounds; Nanoparticles; Graphite; Sulfhydryl Compounds; 0210 nano-technology; Hydrogen; Platinum

We report the development of a highly efficient photocatalytic system by immobilizing high-quality CdS quantum dots and dendritic Pt nanocrystals on thiol-functionalized graphene substrates. We have demonstrated that the use of QDs with compact sizes leads to a dramatically enhanced performance in comparison with their bulk counterparts. Our design allows for systematic examination of the impact of QD sizes and the loading, morphology, and surface coating of the Pt nanocrystal cocatalyst on the H2 evolution activity. It was found that the CdS-Pt binary system has a high photocatalytic efficiency of 1.37 mmol h(-1) for visible light driven H2 evolution, and there was a 30% improvement by introducing the thiolated reduced graphene oxide to form the three-component CdS-Pt-Gcys nanocomposites. The highest H2 evolution rate of 2.15 mmol h(-1) (λ ≥ 420 nm) with a QE of 50.7% was achieved by further photo-annealing of the CdS-Pt-Gcys nanocomposites prior to the photocatalytic reaction.