4.6 Article

The Phase Evolution and Photocatalytic Properties of a Ti-TiO2 Bilayer Thin Film Prepared Using Thermal Oxidation

Journal

COATINGS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/coatings11070808

Keywords

TiO2; bilayer thin films; photocatalytic; thermal oxidation

Funding

  1. Department of Materials Engineering, National Pingtung University of Science and Technology

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The study investigated the structural, optical, and photocatalytic performance of Ti-TiO2 bilayer thin films under different oxidation conditions, showing that the bottom layer of TiO2 significantly influences the phase structure evolution of Ti thin films and that bilayer films exhibit higher photocatalytic activity.
Ti-TiO2 bilayer thin films were successfully prepared onto a glass substrate using magnetron sputtering with different TiO2 bottom layer conditions. These represent a lack of (as-deposited) and full oxygen content (annealed). Single-layer Ti was additionally used as a control. The influence of oxygen diffusion phenomena of the bottom layer of TiO2 to the upper layer of Ti thin films at different oxidation temperatures on structural, optical, and photocatalytic performance was investigated. X-ray diffraction (XRD) results confirmed that the crystalline phases coexisting on thin-film samples oxidized at 450 degrees C were TiO, TiO1.4, (bilayer, as-deposited TiO2), anatase (bilayer, annealed TiO2), and rutile (single and bilayer). This finding showed that the film's phase structure evolution is significantly affected by oxygen diffusion from the bottom layer. Further increasing the thermal oxidation temperature caused a notable decline in the amorphous zone in bilayer thin films based on TEM analysis. Bilayer thin films lead to higher degradation of methylene blue under UV light radiation (63%) than single-layer films (45%) oxidized at 450 degrees C. High photocatalytic activity performance was found in the bilayer annealed TiO2-Ti thin-film sample. This study demonstrates that the bilayer modification strategy promotes the oxygen-induced bottom layer of TiO2 bilayer thin films.

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