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Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity

Layered heterojunction structure with larger interface region for electron migration has attracted much attention in recent years. In this work, layered α-Fe(2)O(3)/Bi(2)WO(6) heterojunctions with strong interlayer interaction were successfully synthesized through a facile in situ growth method. The...

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Autores principales: Xie, Taiping, Liu, Yue, Wang, Haiqiang, Wu, Zhongbiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525269/
https://www.ncbi.nlm.nih.gov/pubmed/31101853
http://dx.doi.org/10.1038/s41598-019-43917-w
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author Xie, Taiping
Liu, Yue
Wang, Haiqiang
Wu, Zhongbiao
author_facet Xie, Taiping
Liu, Yue
Wang, Haiqiang
Wu, Zhongbiao
author_sort Xie, Taiping
collection PubMed
description Layered heterojunction structure with larger interface region for electron migration has attracted much attention in recent years. In this work, layered α-Fe(2)O(3)/Bi(2)WO(6) heterojunctions with strong interlayer interaction were successfully synthesized through a facile in situ growth method. The strong interaction between α-Fe(2)O(3) and Bi(2)WO(6) had resulted in excellent photoelectrochemical performance. It was found that such structure promoted the interfacial photogenerated charges separation according to EIS and Tafel analysis, except for the expansion of visible-light absorption range. PL and TRPL characterizations further demonstrated that the recombination ratio of photoexcited electron-hole pairs was greatly reduced. The toluene photocatalytic degradation tests had showed that α-Fe(2)O(3)/Bi(2)WO(6) composites exhibited much well activity under visible-light irradiation. Especially, 4%-Fe(2)O(3)/Bi(2)WO(6) sample displayed the highest photocatalytic activity, which was around 3 and 4 times higher than that of pure Bi(2)WO(6) and α-Fe(2)O(3). Based on ESR results and free radical trapping experiments, hydroxyl radicals (·OH) and holes (h(+)) were regarded as the main active species. The establishment of Fe(2)O(3)/Bi(2)WO(6) with layered heterojunctions could provide new insights into the construction of novel photocatalysts.
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spelling pubmed-65252692019-05-29 Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity Xie, Taiping Liu, Yue Wang, Haiqiang Wu, Zhongbiao Sci Rep Article Layered heterojunction structure with larger interface region for electron migration has attracted much attention in recent years. In this work, layered α-Fe(2)O(3)/Bi(2)WO(6) heterojunctions with strong interlayer interaction were successfully synthesized through a facile in situ growth method. The strong interaction between α-Fe(2)O(3) and Bi(2)WO(6) had resulted in excellent photoelectrochemical performance. It was found that such structure promoted the interfacial photogenerated charges separation according to EIS and Tafel analysis, except for the expansion of visible-light absorption range. PL and TRPL characterizations further demonstrated that the recombination ratio of photoexcited electron-hole pairs was greatly reduced. The toluene photocatalytic degradation tests had showed that α-Fe(2)O(3)/Bi(2)WO(6) composites exhibited much well activity under visible-light irradiation. Especially, 4%-Fe(2)O(3)/Bi(2)WO(6) sample displayed the highest photocatalytic activity, which was around 3 and 4 times higher than that of pure Bi(2)WO(6) and α-Fe(2)O(3). Based on ESR results and free radical trapping experiments, hydroxyl radicals (·OH) and holes (h(+)) were regarded as the main active species. The establishment of Fe(2)O(3)/Bi(2)WO(6) with layered heterojunctions could provide new insights into the construction of novel photocatalysts. Nature Publishing Group UK 2019-05-17 /pmc/articles/PMC6525269/ /pubmed/31101853 http://dx.doi.org/10.1038/s41598-019-43917-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xie, Taiping
Liu, Yue
Wang, Haiqiang
Wu, Zhongbiao
Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title_full Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title_fullStr Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title_full_unstemmed Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title_short Synthesis of α-Fe(2)O(3)/Bi(2)WO(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
title_sort synthesis of α-fe(2)o(3)/bi(2)wo(6) layered heterojunctions by in situ growth strategy with enhanced visible-light photocatalytic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525269/
https://www.ncbi.nlm.nih.gov/pubmed/31101853
http://dx.doi.org/10.1038/s41598-019-43917-w
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