Please use this identifier to cite or link to this item: https://doi.org/10.1021/cm060450b
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dc.titleSubstrate-assisted crystallization and photocatalytic properties of mesoporous TiO2 thin films
dc.contributor.authorZhang, Yu.
dc.contributor.authorLi, J.
dc.contributor.authorWang, J.
dc.date.accessioned2014-10-07T09:54:17Z
dc.date.available2014-10-07T09:54:17Z
dc.date.issued2006-06-13
dc.identifier.citationZhang, Yu., Li, J., Wang, J. (2006-06-13). Substrate-assisted crystallization and photocatalytic properties of mesoporous TiO2 thin films. Chemistry of Materials 18 (12) : 2917-2923. ScholarBank@NUS Repository. https://doi.org/10.1021/cm060450b
dc.identifier.issn08974756
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86743
dc.description.abstractHighly crystallized mesoporous TiO2 thin films with enhanced photocatalytic activity were synthesized via a substrate-assisted strategy. Three types of substrates, namely, amorphous glass, polycrystalline Pt, and single-crystal Si(111) wafer, were employed to study their effects on the structure of TiO2 films, by using small-angle X-ray scattering (SAXS), transmission electron microscopy (TEM), X-ray diffraction (XRD), a Raman spectrometer, and a UV-vis spectrophotometer. When the substrate was changed from amorphous glass to polycrystalline Pt and then to single-crystal Si(111), a transition in the pore configuration took place from a cubical configuration to cagelike arrays, accompanied by an increase in nanocrystallinity. The observed transitions in pore configuration of mesoporous TiO2 can be accounted for by the differences in nucleation behaviors and surface energy among the substrate systems involved. Mesoporous TiO2 thin films of enhanced nanocrystallinity demonstrate improved photocatalytic activity for degradation of methylene blue (MB) under UV irradiation. They also show photoluminescence at room temperature, which is related to the radiative recombination of excitons. © 2006 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cm060450b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1021/cm060450b
dc.description.sourcetitleChemistry of Materials
dc.description.volume18
dc.description.issue12
dc.description.page2917-2923
dc.description.codenCMATE
dc.identifier.isiut000238048400020
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