Abstract

Titanium dioxide photocatalysts have received a lot of attention during the past decades due to their ability to degrade various organic pollutants to CO2 and H2O, which makes them suitable for use in environmental related fields such as air and water treatment and self-cleaning surfaces. In this work, titania thin films and powders were prepared by a particulate sol–gel route, using titanium tetrachloride (TiCl4) as a precursor. Afterwards, the prepared sols were doped with nitrogen (ammonium nitrate, urea), sulfur (thiourea) and platinum (chloroplatinic acid), coated onto glass substrates by dip-coating, and thermally treated in a muffle furnace to promote crystallization. The resulting thin films were then characterized by various techniques (i.e., TGA-DSC-MS, XRD, BET, XPS, SEM, band gap measurements). The photocatalytic activity of the prepared thin films was determined by measuring the degradation rate of plasmocorinth B (PB), an organic pigment used in the textile industry, which can pose an environmental risk when expelled into wastewater. A kinetic model for adsorption and subsequent degradation was used to fit the experimental data. The results have shown an increase in photocatalytic activity under visible-light illumination of nonmetal and metal doped and co-doped titania thin films compared to an undoped sample.

Highlights

  • In recent years, titanium dioxide (TiO2) has emerged as one of the most widely investigated semiconductors [1]

  • The photocatalytic activity of the prepared thin films was determined by measuring the degradation rate of plasmocorinth B (PB), an organic pigment used in the textile industry, which can pose an environmental risk when expelled into wastewater

  • The results have shown an increase in photocatalytic activity under visible-light illumination of nonmetal and metal doped and co-doped titania thin films compared to an undoped sample

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Summary

Introduction

Titanium dioxide (TiO2) has emerged as one of the most widely investigated semiconductors [1]. By increasing the specific surface area (porosity) of TiO2, the photocatalytic activity can be increased. The specific surface area can be increased by decreasing the particle size of TiO2; it has been shown that the photocatalytic activity does not monotonically increase with decreasing particle size, but rather there exists an optimal particle size for pure nanocrystalline TiO2 [19]. This is due to surface recombination of electron–hole pairs in samples with particle sizes smaller than 6 nm

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