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Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State
W(18)O(49) with a tunable oxidation state was prepared by addition of NaNO(3) or NaBH(4) as a redox agent in the solvothermal system. The addition of redox agents has no influence on the crystallization of W(18)O(49). The obtained W(18)O(49) structures keep their morphology as a bundle of nanowires...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390804/ https://www.ncbi.nlm.nih.gov/pubmed/28413762 http://dx.doi.org/10.1002/open.201600149 |
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author | Fang, Zhenxing Jiao, Shihui Kang, Yutang Pang, Guangsheng Feng, Shouhua |
author_facet | Fang, Zhenxing Jiao, Shihui Kang, Yutang Pang, Guangsheng Feng, Shouhua |
author_sort | Fang, Zhenxing |
collection | PubMed |
description | W(18)O(49) with a tunable oxidation state was prepared by addition of NaNO(3) or NaBH(4) as a redox agent in the solvothermal system. The addition of redox agents has no influence on the crystallization of W(18)O(49). The obtained W(18)O(49) structures keep their morphology as a bundle of nanowires with a regular hexagonal on the cross‐section. W(18)O(49) exhibits strong valence‐dependent absorption features in the near‐IR region. Reduced W(18)O(49) with more W(5+) has a higher concentration of oxygen vacancies, which enhances the localized surface plasmon resonance effect. Reduced W(18)O(49) exhibits a high photothermal conversion efficiency of 59.6 % and has good photothermal stability. |
format | Online Article Text |
id | pubmed-5390804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53908042017-04-14 Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State Fang, Zhenxing Jiao, Shihui Kang, Yutang Pang, Guangsheng Feng, Shouhua ChemistryOpen Full Papers W(18)O(49) with a tunable oxidation state was prepared by addition of NaNO(3) or NaBH(4) as a redox agent in the solvothermal system. The addition of redox agents has no influence on the crystallization of W(18)O(49). The obtained W(18)O(49) structures keep their morphology as a bundle of nanowires with a regular hexagonal on the cross‐section. W(18)O(49) exhibits strong valence‐dependent absorption features in the near‐IR region. Reduced W(18)O(49) with more W(5+) has a higher concentration of oxygen vacancies, which enhances the localized surface plasmon resonance effect. Reduced W(18)O(49) exhibits a high photothermal conversion efficiency of 59.6 % and has good photothermal stability. John Wiley and Sons Inc. 2017-01-18 /pmc/articles/PMC5390804/ /pubmed/28413762 http://dx.doi.org/10.1002/open.201600149 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Fang, Zhenxing Jiao, Shihui Kang, Yutang Pang, Guangsheng Feng, Shouhua Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title | Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title_full | Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title_fullStr | Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title_full_unstemmed | Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title_short | Photothermal Conversion of W(18)O(49) with a Tunable Oxidation State |
title_sort | photothermal conversion of w(18)o(49) with a tunable oxidation state |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390804/ https://www.ncbi.nlm.nih.gov/pubmed/28413762 http://dx.doi.org/10.1002/open.201600149 |
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