A simple particulate sol-gel route to synthesize nanostructural TiO2-Ta2O5 binary oxides and their characteristics

Mohammadi, M. R.; Fray, D. J.; Sadrnezhaad, S. K.; Mohammadi, A.

Abstract

Nanostructured and mesoporous TiO2-Ta2O5 films and powders with various TiO2:Ta2O5 molar ratios and high specific surface area (SSA) have been prepared by a straightforward particulate sol-gel route. Titanium isopropoxide and tantalum ethoxide were used as precursors and hydroxypropyl cellulose (HPC) was used as a polymeric fugitive agent (PFA) in order to increase the SSA. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) revealed that powders contained both hexagonal delta-Ta2O5 and monoclinic beta-Ta2O5 phases, as well as anatase and rutile. It was observed that Ta2O5 retarded anatase-to-rutile transformation. Furthermore, delta ->beta phase transformation temperature increased with decreasing TiO2:Ta2O5 molar ratio. Transmission electron microscope (TEM) analysis also showed that Ta2O5 hindered the crystallisation and crystal growth of the powders. SSA of powders, as measured by Brunauer-Emmett-Teller (BET) analysis, was enhanced by introducing Ta2O5. TiTal 1 binary oxide (TiO2:Ta2O5=50:50 molar ratio) annealed at 500 degrees C produced the smallest crystallite size (3.4nm), the smallest grain size (15 nm), the highest SSA (172 m(2)/g) and the highest roughness. Atomic force microscope (AFM) analysis revealed that columnar-like morphology with nanosized grains was obtained for TiO2-Ta2O5 films. One of the smallest crystallite size and one of the highest SSA reported in the literature is obtained, and they can be used in many applications in areas from optical electronics to gas sensors. (c) 2007 Elsevier B.V. All rights reserved.

Más información

Título según WOS: ID WOS:000249546700002 Not found in local WOS DB
Título de la Revista: MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS
Volumen: 142
Número: 1
Editorial: Elsevier
Fecha de publicación: 2007
Página de inicio: 16
Página final: 27
DOI:

10.1016/j.mseb.2007.06.023

Notas: ISI