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A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions
Optical thermometry based on the up-conversion intensity ratio of thermally coupled levels of rare earth ions has been widely studied to achieve an inaccessible temperature measurement in submicron scale. In this work, a novel optical temperature sensing strategy based on the energy transfer from ch...
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/PMC5519774/ https://www.ncbi.nlm.nih.gov/pubmed/28729660 http://dx.doi.org/10.1038/s41598-017-06421-7 |
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author | Wang, Jing Bu, Yanyan Wang, Xiangfu Seo, Hyo Jin |
author_facet | Wang, Jing Bu, Yanyan Wang, Xiangfu Seo, Hyo Jin |
author_sort | Wang, Jing |
collection | PubMed |
description | Optical thermometry based on the up-conversion intensity ratio of thermally coupled levels of rare earth ions has been widely studied to achieve an inaccessible temperature measurement in submicron scale. In this work, a novel optical temperature sensing strategy based on the energy transfer from charge transfer bands of W-O and Eu-O to Eu(3+)-Dy(3+) ions is proposed. A series of Eu(3+)/Dy(3+) co-doped SrWO(4) is synthesized by the conventional high-temperature solid-state method. It is found that the emission spectra, emission intensity ratio of Dy(3+) (572 nm) and Eu(3+) (615 nm), fluorescence color, lifetime decay curves of Dy(3+) (572 nm) and Eu(3+) (615 nm), and relative and absolute sensitivities of Eu(3+)/Dy(3+) co-doped SrWO(4) are temperature dependent under the 266 nm excitation in the temperature range from 11 K to 529 K. The emission intensity ratio of Dy(3+) (572 nm) and Eu(3+) (615 nm) ions exhibits exponentially relation to the temperature due to the different energy transfer from the charge transfer bands of W-O and Eu-O to Dy(3+) and Eu(3+) ions. In this host, the maximum relative sensitivity S(r) can be reached at 1.71% K(−1), being higher than those previously reported material. It opens a new route to obtain optical thermometry with high sensitivity through using down-conversion fluorescence under ultraviolet excitation. |
format | Online Article Text |
id | pubmed-5519774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55197742017-07-26 A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions Wang, Jing Bu, Yanyan Wang, Xiangfu Seo, Hyo Jin Sci Rep Article Optical thermometry based on the up-conversion intensity ratio of thermally coupled levels of rare earth ions has been widely studied to achieve an inaccessible temperature measurement in submicron scale. In this work, a novel optical temperature sensing strategy based on the energy transfer from charge transfer bands of W-O and Eu-O to Eu(3+)-Dy(3+) ions is proposed. A series of Eu(3+)/Dy(3+) co-doped SrWO(4) is synthesized by the conventional high-temperature solid-state method. It is found that the emission spectra, emission intensity ratio of Dy(3+) (572 nm) and Eu(3+) (615 nm), fluorescence color, lifetime decay curves of Dy(3+) (572 nm) and Eu(3+) (615 nm), and relative and absolute sensitivities of Eu(3+)/Dy(3+) co-doped SrWO(4) are temperature dependent under the 266 nm excitation in the temperature range from 11 K to 529 K. The emission intensity ratio of Dy(3+) (572 nm) and Eu(3+) (615 nm) ions exhibits exponentially relation to the temperature due to the different energy transfer from the charge transfer bands of W-O and Eu-O to Dy(3+) and Eu(3+) ions. In this host, the maximum relative sensitivity S(r) can be reached at 1.71% K(−1), being higher than those previously reported material. It opens a new route to obtain optical thermometry with high sensitivity through using down-conversion fluorescence under ultraviolet excitation. Nature Publishing Group UK 2017-07-20 /pmc/articles/PMC5519774/ /pubmed/28729660 http://dx.doi.org/10.1038/s41598-017-06421-7 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 Wang, Jing Bu, Yanyan Wang, Xiangfu Seo, Hyo Jin A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title | A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title_full | A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title_fullStr | A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title_full_unstemmed | A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title_short | A novel optical thermometry based on the energy transfer from charge transfer band to Eu(3+)-Dy(3+) ions |
title_sort | novel optical thermometry based on the energy transfer from charge transfer band to eu(3+)-dy(3+) ions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519774/ https://www.ncbi.nlm.nih.gov/pubmed/28729660 http://dx.doi.org/10.1038/s41598-017-06421-7 |
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