Abstract

The development and application of well-organized nanostructured materials with high absorption on visible light for application in photoelectrodegradation of polluting organic compounds are challenging problems. This paper presents the formation of nanotubular oxides grown on Ti14wt.%Nb substrate (NT/Ti14wt.%Nb) by an anodizing process, as well as the influence of the temperature in the oxide crystallization and in the photocatalytic activity performance. The oxide layers were characterized by SEM, EDX, Raman, XRD, and photocurrent studies. Electrochemical impedance spectroscopy measurements and polarization curves were also investigated. The diffusion reflectance UV-Vis-NIR spectroscopy assays showed higher absorption in the visible region for Nb-modified TiO2 nanotubes. The characterization of the nanoscale oxide layer grown on Ti14wt.%Nb alloy showed a hybrid (partially Nb-doped) semiconductor behavior with high current density under UV/visible and visible light. Besides that, NT/Ti14wt.%Nb demonstrated greater resistance to corrosion and low recombination of charges compared with TiO2 nanotubes. In general, the results have shown that NT/Ti14wt.%Nb presents a potential for its application in photoelectrocatalytic (PEC) degradation processes. PEC tests of the Reactive Blue 4 (RB4) dye showed total decoloration (k = 0.17 min−1) and 88% degradation under UV/visible light for the oxide layer grown on Ti14wt.%Nb alloy annealed at 450 °C in comparison with those for the oxide layer grown on TiO2 nanotubes.

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.