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In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity
Exploring the full potential use of heterojunction photocatalysts containing bismuth has attracted considerable interest in recent years. Fabrication of well-defined heterojunction photocatalysts with precise modulation of their chemical composition is crucial for tuning their optical properties and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807223/ https://www.ncbi.nlm.nih.gov/pubmed/26997545 http://dx.doi.org/10.1038/srep23435 |
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author | Huang, Yu Wang, Wei Zhang, Qian Cao, Jun-ji Huang, Ru-jin Ho, Wingkei Lee, Shun Cheng |
author_facet | Huang, Yu Wang, Wei Zhang, Qian Cao, Jun-ji Huang, Ru-jin Ho, Wingkei Lee, Shun Cheng |
author_sort | Huang, Yu |
collection | PubMed |
description | Exploring the full potential use of heterojunction photocatalysts containing bismuth has attracted considerable interest in recent years. Fabrication of well-defined heterojunction photocatalysts with precise modulation of their chemical composition is crucial for tuning their optical properties and photocatalytic activity. In this study, we fabricated nanoplate α-Bi(2)O(3)/(BiO)(2)CO(3) heterojunctions through in situ thermal treatment of (BiO)(2)CO(3) nanoplates synthesized using a facile hydrothermal process. Characterization results showed that the as-prepared Bi(2)O(3)/(BiO)(2)CO(3) heterojunctions possessed distinct crystal interface and exhibited pronounced structural and optical modulation, resulting in significant improvement of their photocatalytic activity for NO removal under simulated solar light irradiation compared with pristine (BiO)(2)CO(3). Electron spin resonance spectroscopy showed that ⋅OH radicals were the major reactive species involved in NO degradation, which is consistent with the theoretical analysis. The heterojunction formation can not only broaden the light absorption range but also improve the charge separation of photo-induced electron–hole pairs. This study is an important advancement in the development of semiconductor heterojunctions towards achieving functional photocatalysts. |
format | Online Article Text |
id | pubmed-4807223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48072232016-03-25 In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity Huang, Yu Wang, Wei Zhang, Qian Cao, Jun-ji Huang, Ru-jin Ho, Wingkei Lee, Shun Cheng Sci Rep Article Exploring the full potential use of heterojunction photocatalysts containing bismuth has attracted considerable interest in recent years. Fabrication of well-defined heterojunction photocatalysts with precise modulation of their chemical composition is crucial for tuning their optical properties and photocatalytic activity. In this study, we fabricated nanoplate α-Bi(2)O(3)/(BiO)(2)CO(3) heterojunctions through in situ thermal treatment of (BiO)(2)CO(3) nanoplates synthesized using a facile hydrothermal process. Characterization results showed that the as-prepared Bi(2)O(3)/(BiO)(2)CO(3) heterojunctions possessed distinct crystal interface and exhibited pronounced structural and optical modulation, resulting in significant improvement of their photocatalytic activity for NO removal under simulated solar light irradiation compared with pristine (BiO)(2)CO(3). Electron spin resonance spectroscopy showed that ⋅OH radicals were the major reactive species involved in NO degradation, which is consistent with the theoretical analysis. The heterojunction formation can not only broaden the light absorption range but also improve the charge separation of photo-induced electron–hole pairs. This study is an important advancement in the development of semiconductor heterojunctions towards achieving functional photocatalysts. Nature Publishing Group 2016-03-21 /pmc/articles/PMC4807223/ /pubmed/26997545 http://dx.doi.org/10.1038/srep23435 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Huang, Yu Wang, Wei Zhang, Qian Cao, Jun-ji Huang, Ru-jin Ho, Wingkei Lee, Shun Cheng In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title | In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title_full | In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title_fullStr | In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title_full_unstemmed | In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title_short | In situ Fabrication of α-Bi(2)O(3)/(BiO)(2)CO(3) Nanoplate Heterojunctions with Tunable Optical Property and Photocatalytic Activity |
title_sort | in situ fabrication of α-bi(2)o(3)/(bio)(2)co(3) nanoplate heterojunctions with tunable optical property and photocatalytic activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807223/ https://www.ncbi.nlm.nih.gov/pubmed/26997545 http://dx.doi.org/10.1038/srep23435 |
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