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In situ FTIR studies of the photo-electrochemical behaviour of thermal TiO2 films as a function of temperature

Lookup NU author(s): Professor Paul Christensen, Dr Andrew Hamnett

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Abstract

The photo-electrochemical behaviour of thermal TiO2 films in aqueous methanol electrolytes has been investigated as a function of temperature with in situ Fourier transform infrared (FTIR) spectroscopy. Although the electrochemical behaviour of the films at 10 and 50 °C was apparently identical on the basis of cyclic voltammetry, both in the light and in the dark, investigation with FTIR showed very different product distributions at these two temperatures, which could be correlated with other data, suggesting a significant reduction in methanol adsorption at the higher temperature. The O2 bubble formation observed under irradiation in the absence of methanol at both temperatures was completely suppressed at 10 °C in the presence of methanol, and only observed at higher potentials at 50 °C. Adsorbed methanol was photo-oxidised completely to CO2, but solution-phase methanol was oxidised only to formaldehyde at lower temperatures and to a mixture of the latter and formic acid at 50 °C. An explanation of this second difference, and of the fact that photo-oxidation at the higher temperature could also lead to O2 formation, can be given in terms of the enhanced mobility of adsorbed ·OH species at 50 °C. Finally, a significant number of the spectra obtained were dominated by unusual water-like features; these features can be assigned to changes in the spectral response of water as a function of ionic strength, and considerable caution is needed in the interpretation of such spectra.


Publication metadata

Author(s): Christensen PA, Eameaim J, Hamnett A

Publication type: Article

Publication status: Published

Journal: Physical Chemistry Chemical Physics

Year: 1999

Volume: 1

Issue: 23

Pages: 5315-5321

Print publication date: 01/12/1999

ISSN (print): 1463-9076

ISSN (electronic): 1463-9084

Publisher: Royal Society of Chemistry

URL: http://dx.doi.org/10.1039/a906712d

DOI: 10.1039/a906712d


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