Preparation of Au/TiO sub(2) catalysts from Au(I)-thiosulfate complex and study of their photocatalytic activity for the degradation of methyl orange
Gold loaded on TiO sub(2) (Au/TiO sub(2)) catalysts were prepared using Au(I)-thiosulfate complex (Au(S sub(2)O sub(3)) sub(2) super(3-)) as the gold precursor for the first time. The samples were characterized by UV-vis diffuse reflectance spectra, X-ray diffraction (XRD), transmission electron mic...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2008-03, Vol.79 (4), p.394-401 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Gold loaded on TiO sub(2) (Au/TiO sub(2)) catalysts were prepared using Au(I)-thiosulfate complex (Au(S sub(2)O sub(3)) sub(2) super(3-)) as the gold precursor for the first time. The samples were characterized by UV-vis diffuse reflectance spectra, X-ray diffraction (XRD), transmission electron microscopy (TEM), atomic absorption flame emission spectroscopy (AAS), and X- ray photoelectron spectroscopy (XPS) methods. Using Au(S sub(2)O sub(3)) sub(2) super(3-) as gold precursor, ultra-fine gold nanoparticles with a highly disperse state can be successfully formed on the surface of TiO sub(2). The diameter of Au nanoparticles increases from 1.8 to 3.0 nm with increasing the nominal Au loading from 1% to 8%. The photocatalytic activity of Au/TiO sub(2) catalysts was evaluated from the analysis of the photodegradation of methyl orange (MO). With the similar Au loading, the catalysts prepared with Au(S sub(2)O sub(3)) sub(2) super(3-) precursor exhibit higher photocatalytic activity for methyl orange degradation when compared with the Au/TiO sub(2) catalysts prepared with the methods of deposition-precipitation (DP) and impregnation (IMP). The preparation method has decisive influences on the morphology, size and number of Au nanoparticles loaded on the surface of TiO sub(2) and further affects the photocatalytic activity of the obtained catalysts. |
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ISSN: | 0926-3373 |
DOI: | 10.1016/j.apcatb.2007.11.001 |