4.7 Article Proceedings Paper

TiO2 Processed by pressurized hot solvents as a novel photocatalyst for photocatalytic reduction of carbon dioxide

Journal

APPLIED SURFACE SCIENCE
Volume 391, Issue -, Pages 282-287

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2016.06.061

Keywords

Anatase/brookite nanocomposite; Nanoparticle; Sol-gel preparation; Pressurized hot solvents; Photocatalysis; CO2 reduction

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Anatase-brookite TiO2 photocatalysts were prepared by the sol-gel process controlled within reverse micelles and processing by pressurized hot solvents water/methanol/water (TiO2(M)) and water/ethanol/water (TiO2(E)), as an unconventional alternative to common calcination. The main goal of this work was to prepare anatase-brookite mixtures by processing by two different alcohols (methanol and ethanol) and evaluate the influence of the alcohol on the photocatalytic activity. Prepared photocatalysts were characterized by organic elemental analysis, nitrogen physisorption, XRD, UV vis, photoelectrochemical and spectroelectrochemical measurements and XPS. The prepared photocatalysts efficiency was tested on the photocatalytic reduction of carbon dioxide and compared with commercial TiO2 Evonik P25. Both prepared nanocomposites were more efficient towards methane production but Evonik P25 was the most efficient towards hydrogen generated through water splitting. The higher performance of anatase-brookite mixture towards methane production can be explained by (i) a higher photocatalytic activity of brookite than rutile; (ii) a large surface area of anatase-brookite composites enabling better carbon dioxide adsorption; (iii) the photoinduced electron transfer from the brookite conduction band to the anatase conduction band. On the other hand, a higher production of hydrogen in the presence of Evonik P25 is caused by a better charge separation in anatase-rutile than anatasebrookite phase compositions. TiO2(M) appeared more active than TiO2(E) in the photocatalytic reduction of carbon dioxide due to a lower density of defects created in the crystal lattice. (C) 2016 Elsevier B.V. All rights reserved.

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