Solid-gas phase photo-catalytic behaviour of rutile and TiOn (1<n<2) sub-oxide phases for self-cleaning applications

The solid-gas phase photo-catalytic activities of rutile TiO₂ and TiO n (1 < n < 2) sub-oxide phases have been evaluated. Varying concentrations of Ti 3+ defects were introduced into the rutile polymorph of titanium dioxide through carbo-thermal reduction at temperatures ranging from 350 °C to...

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Veröffentlicht in:Materials 2019-01, Vol.12 (1), p.1-13, Article 170
Hauptverfasser: Nuño, Manuel, Adamaki, Vaia, Tobaldi, D.M., Hortigüela Gallo, Maria, Otero-Irurueta, Gonzalo, Bowen, Christopher, Ball, Richard
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Sprache:eng
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Zusammenfassung:The solid-gas phase photo-catalytic activities of rutile TiO₂ and TiO n (1 < n < 2) sub-oxide phases have been evaluated. Varying concentrations of Ti 3+ defects were introduced into the rutile polymorph of titanium dioxide through carbo-thermal reduction at temperatures ranging from 350 °C to 1300 °C. The resulting sub-oxides formed were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, impedance spectroscopy and UV-visible diffuse reflectance spectroscopy. The presence of Ti 3+ in rutile exposed to high reduction temperatures was confirmed by X-ray diffraction. In addition, a Ti 3+-Ti 4+ system was demonstrated to enhance the photo-catalytic properties of rutile for the degradation of the air pollutants NO₂ and CO₂ under UV irradiation of wavelengths (λ) 376⁻387 nm and 381⁻392 nm. The optimum reduction temperature for photo-catalytic activity was within the range 350⁻400 °C and attributed to improved charge-separation. The materials that were subject to carbo-thermal reduction at temperatures of 350 °C and 400 °C exhibited electrical conductivities over one hundred times higher compared to the non-reduced rutile. The results highlight that sub-oxide phases form an important alternative approach to doping with other elements to improve the photo-catalytic performance of TiO₂. Such materials are important for applications such as self-cleaning where particles can be incorporated into surface coatings.
ISSN:1996-1944
1996-1944
DOI:10.3390/ma12010170