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Controlled synthesis of Bi 2 O 3 /BiOBr/Zn 2 GeO 4 heterojunction photocatalysts with enhanced photocatalytic activity

BiOBr/Zn 2 GeO 4 heterojunctions decorated by Bi 2 O 3 quantum dots ( QD s; named as Bi 2 O 3 /BiOBr/Zn 2 GeO 4 hereafter) with intriguing micro/nanostructures have been constructed via a two‐step hydrothermal route. The compositions, phases, and morphologies of Bi 2 O 3 /BiOBr/Zn 2 GeO 4 were inves...

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Bibliographic Details
Published in:Journal of the American Ceramic Society 2018-12, Vol.101 (12), p.5858-5869
Main Authors: Zhang, Qiang, Pang, Kuan, Xu, Yan
Format: Article
Language:English
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Summary:BiOBr/Zn 2 GeO 4 heterojunctions decorated by Bi 2 O 3 quantum dots ( QD s; named as Bi 2 O 3 /BiOBr/Zn 2 GeO 4 hereafter) with intriguing micro/nanostructures have been constructed via a two‐step hydrothermal route. The compositions, phases, and morphologies of Bi 2 O 3 /BiOBr/Zn 2 GeO 4 were investigated in detail. The light absorption ability, photocurrent responses, and photocatalytic degradation of methylene blue (MB) experiments were performed to evaluate the photocatalytic activity of the micro/nanoheterostructured Bi 2 O 3 /BiOBr/Zn 2 GeO 4 , which present a degradation efficiency of 88% after 240 minutes under light irradiation (λ = 300‐600 nm) over 100 mg Bi 2 O 3 /BiOBr/Zn 2 GeO 4 in a 100 mL, 4 mg/L MB solution. The photocatalytic performance could be retained for at least four runs, indicating its excellent reusability for the degradation of MB in aqueous solution. It is found that the photodegradation of MB over Bi 2 O 3 /BiOBr/Zn 2 GeO 4 is mainly ascribed to a hole oxidation mechanism in combination with a superoxide oxidation process. The high photocatalytic performance of Bi 2 O 3 /BiOBr/Zn 2 GeO 4 upon UV light irradiation can be attributed to the effective charge separation and smoothly transferring of the photogenerated charge carriers throughout the heterojunction. The feasible strategy of preparing Bi 2 O 3 /BiOBr/Zn 2 GeO 4 ternary composites is also of benefit to fabricate other efficient heterojunction catalysts with specific morphologies and properties.
ISSN:0002-7820
1551-2916
DOI:10.1111/jace.15887