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Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization
Heterojunctions modulated internal electric field (IEF) usually result in suboptimal efficiencies in carrier separation and utilization because of the narrow IEF distribution and long migration paths of photocarriers. In this work, we report distinctive bismuth oxyhydroxide compound nanorods (denote...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8368037/ https://www.ncbi.nlm.nih.gov/pubmed/34400649 http://dx.doi.org/10.1038/s41467-021-25261-8 |
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author | Han, Tong Cao, Xing Sun, Kaian Peng, Qing Ye, Chenliang Huang, Aijian Cheong, Weng-Chon Chen, Zheng Lin, Rui Zhao, Di Tan, Xin Zhuang, Zewen Chen, Chen Wang, Dingsheng Li, Yadong |
author_facet | Han, Tong Cao, Xing Sun, Kaian Peng, Qing Ye, Chenliang Huang, Aijian Cheong, Weng-Chon Chen, Zheng Lin, Rui Zhao, Di Tan, Xin Zhuang, Zewen Chen, Chen Wang, Dingsheng Li, Yadong |
author_sort | Han, Tong |
collection | PubMed |
description | Heterojunctions modulated internal electric field (IEF) usually result in suboptimal efficiencies in carrier separation and utilization because of the narrow IEF distribution and long migration paths of photocarriers. In this work, we report distinctive bismuth oxyhydroxide compound nanorods (denoted as BOH NRs) featuring surface-exposed open channels and a simple chemical composition; by simply modifying the bulk anion layers to overcome the limitations of heterojunctions, the bulk IEF could be readily modulated. Benefiting from the unique crystal structure and the localization of valence electrons, the bulk IEF intensity increases with the atomic number of introduced halide anions. Therefore, A low exchange ratio (~10%) with halide anions (I(–), Br(–), Cl(–)) gives rise to a prominent elevation in carrier separation efficiency and better photocatalytic performance for benzylamine coupling oxidation. Here, our work offers new insights into the design and optimization of semiconductor photocatalysts. |
format | Online Article Text |
id | pubmed-8368037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83680372021-09-02 Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization Han, Tong Cao, Xing Sun, Kaian Peng, Qing Ye, Chenliang Huang, Aijian Cheong, Weng-Chon Chen, Zheng Lin, Rui Zhao, Di Tan, Xin Zhuang, Zewen Chen, Chen Wang, Dingsheng Li, Yadong Nat Commun Article Heterojunctions modulated internal electric field (IEF) usually result in suboptimal efficiencies in carrier separation and utilization because of the narrow IEF distribution and long migration paths of photocarriers. In this work, we report distinctive bismuth oxyhydroxide compound nanorods (denoted as BOH NRs) featuring surface-exposed open channels and a simple chemical composition; by simply modifying the bulk anion layers to overcome the limitations of heterojunctions, the bulk IEF could be readily modulated. Benefiting from the unique crystal structure and the localization of valence electrons, the bulk IEF intensity increases with the atomic number of introduced halide anions. Therefore, A low exchange ratio (~10%) with halide anions (I(–), Br(–), Cl(–)) gives rise to a prominent elevation in carrier separation efficiency and better photocatalytic performance for benzylamine coupling oxidation. Here, our work offers new insights into the design and optimization of semiconductor photocatalysts. Nature Publishing Group UK 2021-08-16 /pmc/articles/PMC8368037/ /pubmed/34400649 http://dx.doi.org/10.1038/s41467-021-25261-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Han, Tong Cao, Xing Sun, Kaian Peng, Qing Ye, Chenliang Huang, Aijian Cheong, Weng-Chon Chen, Zheng Lin, Rui Zhao, Di Tan, Xin Zhuang, Zewen Chen, Chen Wang, Dingsheng Li, Yadong Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title | Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title_full | Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title_fullStr | Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title_full_unstemmed | Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title_short | Anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
title_sort | anion-exchange-mediated internal electric field for boosting photogenerated carrier separation and utilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8368037/ https://www.ncbi.nlm.nih.gov/pubmed/34400649 http://dx.doi.org/10.1038/s41467-021-25261-8 |
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