Abstract

Ti O 2 is an excellent material for degradation of many environmental contaminants. Its photocatalytic activity is restricted by UV spectral region that can be extended to visible region using different doping techniques. Effect of fluorine-doping on the optical properties of sol-gel prepared TiO2 thin films is reported. Trifluoroacetic acid (CF3COOH) was used as fluorine source with starting concentrations of 5at.%, 10at.%, and 20at.% F to Ti. Gel films were deposited on SiO2∕soda lime glass substrates by dip-coating technique. After thermal treatment at 450°C fluorine containing TiO2 thin films were obtained. The crystallinity of the films was determined by X-ray diffraction (XRD). The X-ray photoemission spectrometry (XPS) was applied to determine valence state of the dopant and bonding element. The optical constants, namely, refractive index and the extinction coefficient, were obtained by fitting UV-visible theoretical transmittance curves to experimental ones. The simulated transmittance was calculated in the frames of the Forouhi–Bloomer (FB) dispersion model. The values of the FB energy band gap determined as onset of the absorption were compared with Tauc band gap values received by extrapolation of the linear part of the absorption edge. The XRD patterns reflect beginning of the anatase crystallization process. The XPS analysis reveals the presence of fluorine in the films in the form of titanium fluoride, titanium oxyfluorides, and nonstoichiometric TiO2−xFx. The linear part of the absorption edge of TiO2 films for mentioned fluorine concentrations gives slightly increased values of Tauc band gap (∼3.7eV) than that for bulk TiO2(∼3.2eV). Also, its broadening at lower frequencies with a FB band gap ∼2.7eV is observed. The results show that, although the fluorine is incorporated in the TiO2 lattice, it does not affect the crystallinity and band gap of the formed TiO2 film for the F∕Ti ratios used in the starting sols.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.