Abstract

In this study, a series novel NaNbO3/Bi2WO6 heterojunction composites with a type-II alignment were fabricated via a facile wet impregnation method. The as-prepared photocatalysts were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), diffuse reflectance UV-Vis spectroscopy (DRS), photocurrent (PC) and electrochemical impedance spectroscopy (EIS) analyses. The 30 wt% NaNbO3/Bi2WO6 composite exhibited the best performance in the case of degrading rhodamine B (RhB) aqueous solution under visible light irradiation (λ > 410 nm), which was ∼2.5 times and ∼40 times that of pure Bi2WO6 and NaNbO3, respectively. The improved photocatalytic performance was further demonstrated by 2-chlorophenol under the same reaction conditions. This may be attributed to the enhanced electron-hole separation efficiency in Bi2WO6 with the assistance of NaNbO3, as well as the dye-sensitization effect of RhB dye itself. Intermediates produced during the reaction and RhB degradation pathway were investigated as well. Radical quenching experiments revealed h+ played the predominant role; O2·- functioned as well to some degree. Based on experimental results, the potential functioning mechanism was proposed, which is different from previously reported type-II heterostructure systems when Bi2WO6 works as the electron reservoir and O2·- is one of the dominant active species. The as-prepared photocatalyst composite exhibited excellent stability after repetitively running five times. Effects of several operating parameters on the catalyst performance including initial RhB concentration, catalyst dosage, reaction temperature and initial pH were also discussed. This study provides solid evidence for NaNbO3 to be a promising candidate for photocatalysis and gives out a novel photocatalytic mechanism of Bi2WO6-based heterostructures.

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.