Abstract

We report the preparation and application of a heterostructured photoelectrocatalyst comprising carbon nanoparticles (CNPs) and boron codoped BiVO4 and WO3 for the removal of an organic dye pollutant in water. The materials, synthesized by hydrothermal method, were characterized by X-ray diffraction, diffuse reflectance UV–visible spectroscopy, energy-dispersive X-ray spectroscopy, and electron microscopy. The catalysts were immobilized on treated titanium sheets by drop-casting. The fabricated electrodes were characterized by linear sweep voltammetry (LSV) and chronoamperometry. Diffuse reflectance spectroscopy of the catalysts reveals that the incorporation of CNPs and B into the structure of monoclinic BiVO4 enhanced its optical absorption in both UV and visible regions. The LSV measurements carried out in 0.1 M Na2SO4 showed that the BiVO4- and WO3-based photoelectrode demonstrated significant photoactivity. CNP/B-BiVO4 and CNP/B-BiVO4/WO3 photoanodes gave photocurrent densities of approximately 0.83 and 1.79 mA/cm2, respectively, at 1.2 V (vs 3 M Ag/AgCl). The performance of the electrodes toward degradation of orange II dye was in the order BiVO4 < B-BiVO4 < WO3 < CNP-BiVO4 < CNP/B-BiVO4 < CNP/B-BiVO4/WO3, and the apparent rate constants obtained by fitting the experimental data into the Langmuir Hinshelwood kinetic model are 0.0924, 0.1812, 0.254, and 0.845 h–1 for BiVO4, WO3, CNP/B-BiVO4, and CNP/B-BiVO4/WO3, respectively. The chemical oxygen demand abatement after 3 h of electrolysis at the best performing photoanode was 58%. The study showed that BiVO4 and WO3 are promising anodic materials for photoelectrocatalytic water treatment plant.

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.