4.6 Article

Comparative Photo-Electrochemical and Photocatalytic Studies with Nanosized TiO2 Photocatalysts towards Organic Pollutants Oxidation

期刊

CATALYSTS
卷 11, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/catal11030349

关键词

nanosized TiO2; photocatalytic efficiency; photo-electrochemical characterization; environmental remediation

资金

  1. FEDER/Ministerio de Ciencia e Innovacion-Agencia Estatal de Investigacion [RTI2018-102061-B-I00]

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This study investigates the performance of nanosized TiO2 in photo-electrochemical and photocatalytic reactions, showing that nanosized TiO2 has a good effect on the photooxidation reaction of acetone. Different reaction conditions affect the photocatalytic efficiency, and larger-sized samples exhibit lower photoactivity compared to nanosized samples. There is a direct correlation between photocatalytic experiments and photo-electrochemical measurements.
The size of TiO2 can significantly affect both its photocatalytic and photo-electrochemical properties, thus altering the photooxidation of organic pollutants in air or water. In this work, we give an account of the photo-electrochemical and photocatalytic features of some nanosized TiO2 commercial powders towards a model reaction, the photooxidation of acetone. Cyclic voltammograms (CV) of TiO2 particulate electrodes under UV illumination experiments were carried out in either saturated O-2 or N-2 solutions for a direct correlation with the photocatalytic process. In addition, the effect of different reaction conditions on the photocatalytic efficiency under UV light in both aqueous and gaseous phases was also investigated. CV curves with the addition of acetone under UV light showed a negative shift of the photocurrent onset, confirming the efficient transfer of photoproduced reactive oxygen species (ROSs), e.g., hydroxyl radicals or holes to acetone molecules. The photocatalytic experiments showed that the two nano-sized samples exhibit the best photocatalytic performance. The different photoactivity of the larger-sized samples is probably attributed to their morphological differences, affecting both the amount and distribution of free ROSs involved in the photooxidation reaction. Finally, a direct correlation between the photocatalytic measurements in gas phase and the photo-electrochemical measurements in aqueous phase is given, thus evincing the important role of the substrate-surface interaction with similar acetone concentrations.

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