Synthesis and visible-light-derived photocatalysis of titania nanosphere stacking layers prepared by chemical vapor deposition

BACKGROUND: In this study, visible-light-derived photocatalytic activity of metal-doped titanium dioxide nanosphere (TS) stacking layers, prepared by chemical vapor deposition (CVD), was investigated. The as-grown TS spheres, having an average diameter of 100-300 nm, formed a layer-by-layer stacking...

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Published inJournal of chemical technology and biotechnology (1986) Vol. 85; no. 8; pp. 1168 - 1174
Main Authors Hsieh, Chien-Te, Lai, Meng-Hsuan, Pan, Ching
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.08.2010
Wiley
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Summary:BACKGROUND: In this study, visible-light-derived photocatalytic activity of metal-doped titanium dioxide nanosphere (TS) stacking layers, prepared by chemical vapor deposition (CVD), was investigated. The as-grown TS spheres, having an average diameter of 100-300 nm, formed a layer-by-layer stacking layer on a glass substrate. The crystalline structures of the TS samples were of anatase-type.RESULTS: Ultraviolet (UV) absorption confirmed that metallic doping (i.e. Co and Ni) shifted the light absorption of the spheres to the visible-light region. With increasing dopant density, the optical band gap of the nanospheres became narrower, e.g. the smallest band gap of Co-doped TS was 2.61 eV. Both Ni- and Co-doped TS catalysts showed a photocatalytic capability in decomposing organic dyes under visible irradiation. In comparison, Co-doped TiO₂ catalyst not only displays the adsorption capacity, but also the photocatalytic activity higher than the N-doped TiO₂ catalyst.CONCLUSION: This result can be attributed to the fact that the narrower band gap easily generates electron-hole pairs over the TS catalysts under visible irradiation, thus, leading to the higher photocatalytic activity. Accordingly, this study shed some light on the one-step efficient CVD approach to synthesize metal-doped TS catalysts for decomposing dye compounds in aqueous solution. Copyright
Bibliography:http://dx.doi.org/10.1002/jctb.2417
National Science Council (NSC)
Ministry of Education (MOE)
ArticleID:JCTB2417
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ISSN:0268-2575
1097-4660
1097-4660
DOI:10.1002/jctb.2417