Monolithic TiO2 with Controlled Multiscale Porosity via a Template-Free Sol−Gel Process Accompanied by Phase Separation

This article describes the fabrication of multiscale porous nanocrystalline TiO2 monoliths through a one-step method that combines a sol−gel process and phase separation in template-free conditions. A large-dimension monolith with well-defined macropores and a mesostructured anatase-type TiO2 gel sk...

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Bibliographic Details
Published inChemistry of materials Vol. 18; no. 25; pp. 6069 - 6074
Main Authors Konishi, Junko, Fujita, Koji, Nakanishi, Kazuki, Hirao, Kazuyuki
Format Journal Article
LanguageEnglish
Published American Chemical Society 12.12.2006
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Summary:This article describes the fabrication of multiscale porous nanocrystalline TiO2 monoliths through a one-step method that combines a sol−gel process and phase separation in template-free conditions. A large-dimension monolith with well-defined macropores and a mesostructured anatase-type TiO2 gel skeleton is spontaneously obtained by controlling the solution pH during the hydrolysis and polycondensation reactions of titanium alkoxides. The size of the macropores is adjusted by the starting composition, and a crystallized anatase TiO2 skeleton is formed without heat treatment. The use of titanium alkoxide strengthens the gel network by the formation of chemical bonding in the condensation reaction, which yields porous monoliths with higher mechanical strength than for the case of porous monoliths derived from colloidal TiO2 using freeze drying to maintain the porous morphology. The average crystallite size of anatase TiO2 nanocrystals was found to be about 3.6 nm for the dried gel and about 5.0 nm for the gel calcined at 300 °C. As a result of the growth of the anatase TiO2 nanoparticles, the mesopores with a median size of 5.0 nm are obtained. The high surface area (∼150 m2/g) is maintained even after the heat treatment at 300 °C.
Bibliography:istex:22C271F0C1293F62A9C5D1BDA39DF6B500EB6549
ark:/67375/TPS-4D439CRN-3
ISSN:0897-4756
1520-5002
DOI:10.1021/cm0617485