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Decomposition of highly persistent perfluorooctanoic acid by hollow Bi/BiOI1-xFx: Synergistic effects of surface plasmon resonance and modified band structures
[Display omitted] •Bi/BiOI1-xFx hollow microspheres were constructed via one-step hydrothermal method.•Doping with F atoms changed the crystal structure and reduced band gaps of BiOI.•The hollow structure favored the light absorption and enhanced the surface areas.•The Bi-SPR effectively hindered th...
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Published in: | Journal of hazardous materials 2021-01, Vol.402, p.123459, Article 123459 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Bi/BiOI1-xFx hollow microspheres were constructed via one-step hydrothermal method.•Doping with F atoms changed the crystal structure and reduced band gaps of BiOI.•The hollow structure favored the light absorption and enhanced the surface areas.•The Bi-SPR effectively hindered the recombination of the photo-excited charges.•O2− was the main active species responsible for PFOA degradation.
Perfluorooctanoic acid (PFOA) is highly stable due to the strong CF bond and extremely difficult to be removed by conventional photocatalysts. In this study, Bi doped BiOI1-xFx solid solutions with hollow microsphere structure were prepared through a facile one-step hydrothermal method. Compared with pure BiOI and BiOF, the band gap of the Bi/BiOI1-xFx solid solutions was significantly reduced, thus promoting the visible light absorbance. The cavity structure of the BiOI1-xFx solid solutions enhanced the surface areas and active sites for reaction. The local electromagnetic field dominated by surface plasmon resonance (SPR) effect of Bi metal on the surface favored the separation of the photoinduced charge pairs. As a consequence, Bi/BiOI0.8F0.2 (x = 0.20, the doping amount of fluorine was 20 %) composite displayed the best photocatalytic performance for decomposing PFOA, and 40 mg/L PFOA could be removed within 2 h illumination. The degradation rate constant (k = 0.0375 min−1) of PFOA by Bi/BiOI0.8F0.2 was about tenfold of that by pure BiOI and BiOF. Superoxide radical (·O2-) predominated in the degradation of PFOA by Bi/BiOI0.8F0.2, and the possible degradation pathway of PFOA by Bi/BiOI0.8F0.2 was proposed. This work provides a highly efficient catalyst for the practical application in removal of highly persistent PFOA. |
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ISSN: | 0304-3894 1873-3336 |
DOI: | 10.1016/j.jhazmat.2020.123459 |