Abstract
To a large extent, future technological progress relies on the study−development of advanced materials with new and/or improved properties. The semiconductors titanium oxynitride (TixOyNz) and titanium dioxide (TiO2) perfectly meet these requirements in the sense that their main chemical and structural properties can be customized, leading to successful contributions in optics, electronics, catalysis, bactericides surfaces, and photovoltaics applications, for instance. Motivated by these aspects, this paper reports on the structure and optical bandgap of TixOyNz, as obtained by Raman scattering and optical transmittance spectroscopy, respectively. The study comprises a set of films produced by N2-plasma Ti sputtering and subsequently thermal annealed in an atmosphere of oxygen flux. As the thermal treatments advance, the Raman spectra indicate a gradual transformation of the films from amorphous+(nano/micro-)crystalline TixOyNz to the crystalline Rutile phase of TiO2 (R-TiO2). Consistent with these structural changes, the optical bandgap of the films decreases from ∼ 3.2 to 2.5 eV, i.e., across part of the ultraviolet−blue spectral region. The analysis of the experimental data confirms the importance of nitrogen (in the early stages of sample preparation) on the achievement of R-TiO2 in a continuous and controllable way. Therefore, this paper shows the suitability of the TixOyNz compound to produce films with well-defined crystalline TiO2-related structures and specific optical bandgap values.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.