Synthesis and Characterization of WO3/Graphene Nanocomposites for Enhanced Photocatalytic Activities by One-Step In-Situ Hydrothermal Reaction

被引:68
作者
Hu, Xiaoxiao [1 ]
Xu, Peiquan [1 ]
Gong, Hongying [1 ]
Yin, Guotao [1 ]
机构
[1] Shanghai Univ Engn Sci, Coll Mat Engn, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
WO3/GR nanocomposites; hydrothermal method; photocatalysis; visible light; SPRAY-PYROLYSIS; CHARGE-TRANSFER; WO3; NANORODS; GRAPHENE; COMPOSITES; OXIDE; PERFORMANCE; REDUCTION; NANOPARTICLES; DEGRADATION;
D O I
10.3390/ma11010147
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tungsten trioxide (WO3) nanorods are synthesized on the surface of graphene (GR) sheets by using a one-step in-situ hydrothermal method employing sodium tungstate (Na2WO4 center dot 2H(2)O) and graphene oxide (GO) as precursors. The resulting WO3/GR nanocomposites are characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy, scanning electron microscopy and X-ray photoelectron spectroscopy. The results confirm that the interface between WO3 nanorod and graphene contains chemical bonds. The enhanced optical absorption properties are measured by UV-vis diffuse reflectance spectra. The photocatalytic activity of the WO3/GR nanocomposites under visible light is evaluated by the photodegradation of methylene blue, where the degradation rate of WO3/GR nanocomposites is shown to be double that of pure WO3. This is attributed to the synergistic effect of graphene and the WO3 nanorod, which greatly enhances the photocatalytic performance of the prepared sample, reduces the recombination of the photogenerated electron-hole pairs and increases the visible light absorption efficiency. Finally, the photocatalytic mechanism of the WO3/GR nanocomposites is presented. The synthesis of the prepared sample is convenient, direct and environmentally friendly. The study reports a highly efficient composite photocatalyst for the degradation of contaminants that can be applied to cleaning up the environment.
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页数:16
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