Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/100812
Title: High quality graphene oxide–CdS–Pt nanocomposites for efficient photocatalytic hydrogen evolution
Authors: Gao, Peng
Liu, Jincheng
Lee, Siew Siang
Zhang, Tong
Sun, Darren Delai
Keywords: DRNTU::Engineering::Materials::Ecomaterials
Issue Date: 2011
Source: Gao, P., Liu, J., Lee, S., Zhang, T., & Sun, D. D. (2011). High quality graphene oxide-CdS-Pt nanocomposites for efficient photocatalytic hydrogen evolution. Journal of Materials Chemistry, 22, 2292-2298.
Series/Report no.: Journal of materials chemistry
Abstract: Graphene oxide–CdS–Pt (GO–CdS–Pt) nanocomposites with different amounts of Pt nanoparticles were successfully synthesized via the formic acid reduction process followed by a two-phase mixing method. The morphology, crystal phase and optical properties of obtained composites were well characterized by atomic force microscopy (AFM), transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-vis spectroscopy, Fourier transform IR spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), respectively. The photocatalytic activity of GO–CdS–Pt composites for hydrogen generation was investigated. The results show that the GO–CdS–Pt composite containing 0.5 at% of Pt exhibits the highest hydrogen evolution rate of 123 mL h 1 g 1 with strong photostability, which is about 2.5 times higher than that of GO–CdS and 10.3 times higher than that of CdS. The increased photocatalytic hydrogen generation efficiency is attributed to the effective charge separation and decreased anti-recombination with the addition of GO and Pt, as well as the low overpotential of Pt for water splitting. Our findings pave a way to design multi-component graphene-based composites for highly efficient H2 generation and other applications.
URI: https://hdl.handle.net/10356/100812
http://hdl.handle.net/10220/7455
ISSN: 0959-9428
DOI: 10.1039/c2jm15624e
Schools: School of Civil and Environmental Engineering 
Rights: © 2011 The Royal Society of Chemistry. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of Materials Chemistry, The Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [DOI: http://dx.doi.org/10.1039/c2jm15624e].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:CEE Journal Articles

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