Facile construction of flower-like bismuth oxybromide/bismuth oxide formate p-n heterojunctions with significantly enhanced photocatalytic performance under visible light
[Display omitted] Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient ability for degrading toxic pollutants. Herein, visible-light-driven (VLD) BiOBr/BiOCOOH p-n heterojunction photocatalysts w...
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Published in | Journal of colloid and interface science Vol. 548; pp. 12 - 19 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.07.2019
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Subjects | |
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Abstract | [Display omitted]
Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient ability for degrading toxic pollutants. Herein, visible-light-driven (VLD) BiOBr/BiOCOOH p-n heterojunction photocatalysts were prepared via an in-situ anion-exchange route. Through controlling the addition of KBr, we synthesized a series of BiOBr/BiOCOOH p-n heterojunctions with a different BiOBr loading. During the process, BiOBr production and homogeneous deposition on BiOCOOH with close interfacial interactions were realized by employing BiOCOOH microspheres as the self-sacrificing template. Compared to bare BiOBr and BiOCOOH, such p-n heterojunctions displayed dramatically strengthened performance in decomposing the industrial dye (rhodamine B, RhB) and antibiotic (tetracycline chloride, TC) under the irradiation of visible light. Among them, BiOBr/BiOCOOH p-n heterojunction with a BiOBr/BiOCOOH theoretical molar ratio of 0.6/0.4 (0.6Br-Bi) achieved the highest performance. Moreover, 0.6Br-Bi showed a good durability, indicating BiOBr/BiOCOOH p-n heterojunction possessed an excellently stable photocatalytic activity. Such an efficient and stable photocatalytic performance was mainly due to the formation of p-n heterojunctions which can profoundly improve the visible-light absorption and significantly depress the recombination of charge carriers. Trapping experiments and ESR tests verified that superoxide free radicals (O2−) and photogenerated hole (h+) played a significant role in RhB degradation. This research affords a promising p-n heterojunction catalyst for wastewater treatment. |
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AbstractList | Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient ability for degrading toxic pollutants. Herein, visible-light-driven (VLD) BiOBr/BiOCOOH p-n heterojunction photocatalysts were prepared via an in-situ anion-exchange route. Through controlling the addition of KBr, we synthesized a series of BiOBr/BiOCOOH p-n heterojunctions with a different BiOBr loading. During the process, BiOBr production and homogeneous deposition on BiOCOOH with close interfacial interactions were realized by employing BiOCOOH microspheres as the self-sacrificing template. Compared to bare BiOBr and BiOCOOH, such p-n heterojunctions displayed dramatically strengthened performance in decomposing the industrial dye (rhodamine B, RhB) and antibiotic (tetracycline chloride, TC) under the irradiation of visible light. Among them, BiOBr/BiOCOOH p-n heterojunction with a BiOBr/BiOCOOH theoretical molar ratio of 0.6/0.4 (0.6Br-Bi) achieved the highest performance. Moreover, 0.6Br-Bi showed a good durability, indicating BiOBr/BiOCOOH p-n heterojunction possessed an excellently stable photocatalytic activity. Such an efficient and stable photocatalytic performance was mainly due to the formation of p-n heterojunctions which can profoundly improve the visible-light absorption and significantly depress the recombination of charge carriers. Trapping experiments and ESR tests verified that superoxide free radicals (O
) and photogenerated hole (h
) played a significant role in RhB degradation. This research affords a promising p-n heterojunction catalyst for wastewater treatment. Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient ability for degrading toxic pollutants. Herein, visible-light-driven (VLD) BiOBr/BiOCOOH p-n heterojunction photocatalysts were prepared via an in-situ anion-exchange route. Through controlling the addition of KBr, we synthesized a series of BiOBr/BiOCOOH p-n heterojunctions with a different BiOBr loading. During the process, BiOBr production and homogeneous deposition on BiOCOOH with close interfacial interactions were realized by employing BiOCOOH microspheres as the self-sacrificing template. Compared to bare BiOBr and BiOCOOH, such p-n heterojunctions displayed dramatically strengthened performance in decomposing the industrial dye (rhodamine B, RhB) and antibiotic (tetracycline chloride, TC) under the irradiation of visible light. Among them, BiOBr/BiOCOOH p-n heterojunction with a BiOBr/BiOCOOH theoretical molar ratio of 0.6/0.4 (0.6Br-Bi) achieved the highest performance. Moreover, 0.6Br-Bi showed a good durability, indicating BiOBr/BiOCOOH p-n heterojunction possessed an excellently stable photocatalytic activity. Such an efficient and stable photocatalytic performance was mainly due to the formation of p-n heterojunctions which can profoundly improve the visible-light absorption and significantly depress the recombination of charge carriers. Trapping experiments and ESR tests verified that superoxide free radicals (O2-) and photogenerated hole (h+) played a significant role in RhB degradation. This research affords a promising p-n heterojunction catalyst for wastewater treatment. [Display omitted] Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient ability for degrading toxic pollutants. Herein, visible-light-driven (VLD) BiOBr/BiOCOOH p-n heterojunction photocatalysts were prepared via an in-situ anion-exchange route. Through controlling the addition of KBr, we synthesized a series of BiOBr/BiOCOOH p-n heterojunctions with a different BiOBr loading. During the process, BiOBr production and homogeneous deposition on BiOCOOH with close interfacial interactions were realized by employing BiOCOOH microspheres as the self-sacrificing template. Compared to bare BiOBr and BiOCOOH, such p-n heterojunctions displayed dramatically strengthened performance in decomposing the industrial dye (rhodamine B, RhB) and antibiotic (tetracycline chloride, TC) under the irradiation of visible light. Among them, BiOBr/BiOCOOH p-n heterojunction with a BiOBr/BiOCOOH theoretical molar ratio of 0.6/0.4 (0.6Br-Bi) achieved the highest performance. Moreover, 0.6Br-Bi showed a good durability, indicating BiOBr/BiOCOOH p-n heterojunction possessed an excellently stable photocatalytic activity. Such an efficient and stable photocatalytic performance was mainly due to the formation of p-n heterojunctions which can profoundly improve the visible-light absorption and significantly depress the recombination of charge carriers. Trapping experiments and ESR tests verified that superoxide free radicals (O2−) and photogenerated hole (h+) played a significant role in RhB degradation. This research affords a promising p-n heterojunction catalyst for wastewater treatment. |
Author | Liu, Jianshe Liu, Yanping Li, Shijie Ge, Yaming Jiang, Wei Chen, Jialin |
Author_xml | – sequence: 1 givenname: Shijie surname: Li fullname: Li, Shijie organization: Key Laboratory of Key Technical Factors in Zhejiang Seafood Health Hazards, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China – sequence: 2 givenname: Jialin surname: Chen fullname: Chen, Jialin organization: Key Laboratory of Key Technical Factors in Zhejiang Seafood Health Hazards, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China – sequence: 3 givenname: Wei surname: Jiang fullname: Jiang, Wei email: jiangwei_zjou@163.com organization: Key Laboratory of Key Technical Factors in Zhejiang Seafood Health Hazards, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China – sequence: 4 givenname: Yanping surname: Liu fullname: Liu, Yanping organization: College of Marine Science and Technology, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China – sequence: 5 givenname: Yaming surname: Ge fullname: Ge, Yaming email: geyaming@126.com organization: Key Laboratory of Key Technical Factors in Zhejiang Seafood Health Hazards, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China – sequence: 6 givenname: Jianshe surname: Liu fullname: Liu, Jianshe organization: State Environmental Protection Engineering Center for Pollution Treatment and Control in Textile Industry, College of Environmental Science and Engineering, Donghua University, Shanghai 201620, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30978591$$D View this record in MEDLINE/PubMed |
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Keywords | Anion exchange Visible light Photocatalysis BiOBr/BiOCOOH p-n Heterojunction |
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Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts... Visible-light harvesting ability and charge separation efficiency are two pivotal factors for the design and construction of photocatalysts with an efficient... |
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SubjectTerms | Anion exchange BiOBr/BiOCOOH p-n Heterojunction Photocatalysis Visible light |
Title | Facile construction of flower-like bismuth oxybromide/bismuth oxide formate p-n heterojunctions with significantly enhanced photocatalytic performance under visible light |
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