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Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation
A series of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite films were fabricated and immobilized by validated preparation technique. The chemical composition and phase, optical, SPR effect and pore-structure properties together with the morphology of as-prepared composite film are well-characterized....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725600/ https://www.ncbi.nlm.nih.gov/pubmed/29229975 http://dx.doi.org/10.1038/s41598-017-17221-4 |
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author | Lu, Nan Wang, Yaqi Ning, Shiqi Zhao, Wenjing Qian, Min Ma, Ying Wang, Jia Fan, Lingyun Guan, Jiunian Yuan, Xing |
author_facet | Lu, Nan Wang, Yaqi Ning, Shiqi Zhao, Wenjing Qian, Min Ma, Ying Wang, Jia Fan, Lingyun Guan, Jiunian Yuan, Xing |
author_sort | Lu, Nan |
collection | PubMed |
description | A series of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite films were fabricated and immobilized by validated preparation technique. The chemical composition and phase, optical, SPR effect and pore-structure properties together with the morphology of as-prepared composite film are well-characterized. The multi-synergies of as-prepared composite films were gained by combined action of electron-capture action via H(3)PW(12)O(40), visible-response induced by Ag, and Schottky-junction formed between TiO(2)-Ag. Under simulated sunlight, the maximal K (app) of o-chlorophenol (o-CP) reached 0.0075 min(−1) which was 3.95-fold larger than that of TiO(2) film, while it was restrained obviously under acid condition. In the photocatalytic degradation process, ·OH and ·O(2) (−) attacked preferentially ortho and para position of o-CP molecule, and accordingly the specific degradation pathways were speculated. The novel composite film exhibited an excellent applicability due to self-regeneration of H(3)PW(12)O(40), well-protection of metal Ag° and favorable immobilization. |
format | Online Article Text |
id | pubmed-5725600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57256002017-12-13 Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation Lu, Nan Wang, Yaqi Ning, Shiqi Zhao, Wenjing Qian, Min Ma, Ying Wang, Jia Fan, Lingyun Guan, Jiunian Yuan, Xing Sci Rep Article A series of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite films were fabricated and immobilized by validated preparation technique. The chemical composition and phase, optical, SPR effect and pore-structure properties together with the morphology of as-prepared composite film are well-characterized. The multi-synergies of as-prepared composite films were gained by combined action of electron-capture action via H(3)PW(12)O(40), visible-response induced by Ag, and Schottky-junction formed between TiO(2)-Ag. Under simulated sunlight, the maximal K (app) of o-chlorophenol (o-CP) reached 0.0075 min(−1) which was 3.95-fold larger than that of TiO(2) film, while it was restrained obviously under acid condition. In the photocatalytic degradation process, ·OH and ·O(2) (−) attacked preferentially ortho and para position of o-CP molecule, and accordingly the specific degradation pathways were speculated. The novel composite film exhibited an excellent applicability due to self-regeneration of H(3)PW(12)O(40), well-protection of metal Ag° and favorable immobilization. Nature Publishing Group UK 2017-12-11 /pmc/articles/PMC5725600/ /pubmed/29229975 http://dx.doi.org/10.1038/s41598-017-17221-4 Text en © The Author(s) 2017 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 Lu, Nan Wang, Yaqi Ning, Shiqi Zhao, Wenjing Qian, Min Ma, Ying Wang, Jia Fan, Lingyun Guan, Jiunian Yuan, Xing Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title | Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title_full | Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title_fullStr | Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title_full_unstemmed | Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title_short | Design of plasmonic Ag-TiO(2)/H(3)PW(12)O(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
title_sort | design of plasmonic ag-tio(2)/h(3)pw(12)o(40) composite film with enhanced sunlight photocatalytic activity towards o-chlorophenol degradation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725600/ https://www.ncbi.nlm.nih.gov/pubmed/29229975 http://dx.doi.org/10.1038/s41598-017-17221-4 |
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