Issue 39, 2009

A versatile approach to the fabrication of TiO2nanostructures with reverse morphology and mesoporous Ag/TiO2 thin films via cooperative PS-b-PEO self-assembly and a sol-gel process

Abstract

Hybrid titanium dioxide (TiO2) nanostructures with engineered morphologies were produced by a simple synthetic approach based on cooperative sol-gel chemistry and self-assembly of amphiphilic poly(styrene-block-ethylene oxide) (PS-b-PEO) block copolymer (BCP) viaspin-coating common solutions of BCP and inorganic precursors. TiO2nanostructures with two extreme reverse morphologies, i.e., TiO2 dot-in-PS matrix and PS dot-in-TiO2 matrix, were obtained by increasing the volumetric ratio of the TiO2 sol-gel precursor from 10 to 50 vol%. Incorporation of silver nitrate into the TiO2 matrix afforded a hybrid Ag/TiO2 thin film with hexagonally packed arrays of PS nanodots. Upon removal of the PS-b-PEO template from the initial hybrid films by UV treatment, inorganic nanostructures having the same lateral morphologies as the initial films were derived. Among the structures investigated, the Ag/TiO2 mesoporous film exhibited the best photocatalytic performance. The surface/internal morphology and the mechanism of structural evolution were investigated by atomic force microscopy (AFM), transmission electron microscopy (TEM), and grazing-incidence small-angle X-ray scattering (GISAXS).

Graphical abstract: A versatile approach to the fabrication of TiO2nanostructures with reverse morphology and mesoporous Ag/TiO2 thin films via cooperative PS-b-PEO self-assembly and a sol-gel process

Supplementary files

Article information

Article type
Paper
Submitted
20 Apr 2009
Accepted
29 Jul 2009
First published
25 Aug 2009

J. Mater. Chem., 2009,19, 7245-7250

A versatile approach to the fabrication of TiO2nanostructures with reverse morphology and mesoporous Ag/TiO2 thin films via cooperative PS-b-PEO self-assembly and a sol-gel process

M. Cha, C. Shin, D. Kannaiyan, Y. H. Jang, S. T. Kochuveedu, D. Y. Ryu and D. H. Kim, J. Mater. Chem., 2009, 19, 7245 DOI: 10.1039/B907922J

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