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Preparation and characterization of direct Z-scheme photocatalyst Bi2O3/NaNbO3 and its reaction mechanism

•A highly active Bi2O3/NaNbO3 photocatalyst was prepared by a facile ball milling.•The results revealed that Bi2O3/NaNbO3 is characteristic of Z-scheme photocatalyst.•The rate constant of RhB for Bi2O3/NaNbO3 is 6.3 times that of pure NaNbO3.•The e− in the CB of Bi2O3 and h+ in the VB of NaNbO3 are...

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Bibliographic Details
Published in:Applied surface science 2014-02, Vol.292, p.357-366
Main Authors: Chen, Shifu, Hu, Yingfei, Ji, Lei, Jiang, Xiaoliang, Fu, Xianliang
Format: Article
Language:English
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Summary:•A highly active Bi2O3/NaNbO3 photocatalyst was prepared by a facile ball milling.•The results revealed that Bi2O3/NaNbO3 is characteristic of Z-scheme photocatalyst.•The rate constant of RhB for Bi2O3/NaNbO3 is 6.3 times that of pure NaNbO3.•The e− in the CB of Bi2O3 and h+ in the VB of NaNbO3 are quickly combined.•The e− in the CB of NaNbO3 and h+ in the VB of Bi2O3 produce •O2− and •OH, respectively. In this paper, highly active Bi2O3/NaNbO3 photocatalyst was prepared by a facile ball milling method using NaNbO3 and Bi2O3 as precursors. The photocatalyst was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectra (XPS), and Brunauer–Emmett–Teller (BET) surface areas. The photocatalytic activity was evaluated by photocatalytic oxidation of rhodamine B (RhB). The results showed that the photodegradation rate of RhB for Bi2O3(5.0wt%)/NaNbO3 photocatalyst is 6.3 times that of pure NaNbO3. The optimum percentage of doped Bi2O3 is 5.0wt%. And the composite photocatalyst exhibits good stability. Based on the results of characterization by determining reactive species, terephthalic acid photoluminescence probing technique (TA-PL), and electron spin resonance (ESR) technology, it is proposed that the Bi2O3/NaNbO3 has the characteristic of direct Z-scheme type photocatalyst. The mechanism of increased photocatalytic activity was also discussed.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2013.11.144