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We demonstrate an aqueous solution method for the synthesis of a Ag–TiO2–reduced graphene oxide (rGO) hybrid nanostructure (NS) in which the Ag and TiO2 particles are well dispersed on the rGO sheet. The Ag–TiO2–rGO NS was then used as a template to synthesize Pt–TiO2–rGO NS. The resulting hybrid NSs were characterized by transmission electron microscopy (TEM), high-resolution TEM (HRTEM), energy-dispersive X-ray (EDX) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, UV–vis spectroscopy, Raman spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), and catalytic studies. It was found that TiO2–rGO, Ag–TiO2–rGO and Pt–TiO2–rGO NSs all show catalytic activity for the reduction of p-nitrophenol to p-aminophenol by NaBH4, and that Pt–TiO2–rGO NS exhibits the highest catalytic activity as well as excellent stability and easy recyclability.
We demonstrate an aqueous solution method for the synthesis of a Ag–TiO2–reduced graphene oxide (rGO) hybrid nanostructure (NS) in which the Ag and TiO2 particles are well dispersed on the rGO sheet. The Ag–TiO2–rGO NS was then used as a template to synthesize Pt–TiO2–rGO NS. The resulting hybrid NSs were characterized by transmission electron microscopy (TEM), high-resolution TEM (HRTEM), energy-dispersive X-ray (EDX) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, UV–vis spectroscopy, Raman spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), and catalytic studies. It was found that TiO2–rGO, Ag–TiO2–rGO and Pt–TiO2–rGO NSs all show catalytic activity for the reduction of p-nitrophenol to p-aminophenol by NaBH4, and that Pt–TiO2–rGO NS exhibits the highest catalytic activity as well as excellent stability and easy recyclability.
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This work was supported by the National Natural Science Foundation of China (No. 20820102037) and the National Basic Research Program of China (973 Program) (Nos. 2009CB930100 and 2010CB933600). Dr. Ping Wang acknowledges partial financial support from the China Postdoctoral Science Foundation (No. 20090461047).