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BiOBrxI1−x/BiOBr heterostructure engineering for efficient molecular oxygen activation
The both enhanced excition and carrier photocatalysis of BiOBr/BiOBrxI1−x resulted efficient molecular oxygen activation for oilfield waste water treatment and organic pollutants (BPA, RhB and phenol) photodegradation. [Display omitted] •# BiOBrxI1−x/BiOBr heterostructure was in-situ synthesized.•#...
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Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2019-01, Vol.356, p.34-42 |
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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: | The both enhanced excition and carrier photocatalysis of BiOBr/BiOBrxI1−x resulted efficient molecular oxygen activation for oilfield waste water treatment and organic pollutants (BPA, RhB and phenol) photodegradation.
[Display omitted]
•# BiOBrxI1−x/BiOBr heterostructure was in-situ synthesized.•# BiOBrxI1−x/BiOBr showed effective activity for wastewater treatment.•# Exciton and carrier photocatalytic processes was found.
The BiOBrxI1−x/BiOBr heterojunction structural photocatalyst was constructed successfully in this work and it was formed by the BiOBrxI1−x solid solution coupling with the BiOBr monomer, which was determined by efficient characterizations. For the photocatalytic property, The BiOBrxI1−x/BiOBr could degrade some organic pollutants efficiently and the oilfield produced waste water treatment efficiency of it was ideal. The reason for its enhanced photocatalytic property was also explored. Through ESR tests, trapping experiments and other efficient methods, the enhanced molecular oxygen activation capacity of induced 1O2 and O2− photogeneration by BiOBrxI1−x solid solution structure and heterostructure in one photocatalyst was confirmed, respectively. This work provided a new thought for enhanced molecular oxygen activation capacity of bismuth oxyhalide photocatalysts. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2018.09.006 |