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New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization
Phosphor-converted white-light-emitting diodes (pc-WLED) have been extensively employed as solid-state lighting sources, which have a very important role in people’s daily lives. However, due to the scarcity of the red component, it is difficult to realize warm white light efficiently. Hence, red-em...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351663/ https://www.ncbi.nlm.nih.gov/pubmed/30728955 http://dx.doi.org/10.1038/s41377-019-0126-1 |
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author | Wei, Yi Xing, Gongcheng Liu, Kang Li, Guogang Dang, Peipei Liang, Sisi Liu, Min Cheng, Ziyong Jin, Dayong Lin, Jun |
author_facet | Wei, Yi Xing, Gongcheng Liu, Kang Li, Guogang Dang, Peipei Liang, Sisi Liu, Min Cheng, Ziyong Jin, Dayong Lin, Jun |
author_sort | Wei, Yi |
collection | PubMed |
description | Phosphor-converted white-light-emitting diodes (pc-WLED) have been extensively employed as solid-state lighting sources, which have a very important role in people’s daily lives. However, due to the scarcity of the red component, it is difficult to realize warm white light efficiently. Hence, red-emitting phosphors are urgently required for improving the illumination quality. In this work, we develop a novel orangish-red La(4)GeO(8):Bi(3+) phosphor, the emission peak of which is located at 600 nm under near-ultraviolet (n-UV) light excitation. The full width at half maximum (fwhm) is 103 nm, the internal quantum efficiency (IQE) exceeds 88%, and the external quantum efficiency (EQE) is 69%. According to Rietveld refinement analysis and density functional theory (DFT) calculations, Bi(3+) ions randomly occupy all La sites in orthorhombic La(4)GeO(8). Importantly, the oxygen-vacancy-induced electronic localization around the Bi(3+) ions is the main reason for the highly efficient orangish-red luminescence. These results provide a new perspective and insight from the local electron structure for designing inorganic phosphor materials that realize the unique luminescence performance of Bi(3+) ions. |
format | Online Article Text |
id | pubmed-6351663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63516632019-02-06 New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization Wei, Yi Xing, Gongcheng Liu, Kang Li, Guogang Dang, Peipei Liang, Sisi Liu, Min Cheng, Ziyong Jin, Dayong Lin, Jun Light Sci Appl Article Phosphor-converted white-light-emitting diodes (pc-WLED) have been extensively employed as solid-state lighting sources, which have a very important role in people’s daily lives. However, due to the scarcity of the red component, it is difficult to realize warm white light efficiently. Hence, red-emitting phosphors are urgently required for improving the illumination quality. In this work, we develop a novel orangish-red La(4)GeO(8):Bi(3+) phosphor, the emission peak of which is located at 600 nm under near-ultraviolet (n-UV) light excitation. The full width at half maximum (fwhm) is 103 nm, the internal quantum efficiency (IQE) exceeds 88%, and the external quantum efficiency (EQE) is 69%. According to Rietveld refinement analysis and density functional theory (DFT) calculations, Bi(3+) ions randomly occupy all La sites in orthorhombic La(4)GeO(8). Importantly, the oxygen-vacancy-induced electronic localization around the Bi(3+) ions is the main reason for the highly efficient orangish-red luminescence. These results provide a new perspective and insight from the local electron structure for designing inorganic phosphor materials that realize the unique luminescence performance of Bi(3+) ions. Nature Publishing Group UK 2019-01-30 /pmc/articles/PMC6351663/ /pubmed/30728955 http://dx.doi.org/10.1038/s41377-019-0126-1 Text en © The Author(s) 2019 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 Wei, Yi Xing, Gongcheng Liu, Kang Li, Guogang Dang, Peipei Liang, Sisi Liu, Min Cheng, Ziyong Jin, Dayong Lin, Jun New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title | New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title_full | New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title_fullStr | New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title_full_unstemmed | New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title_short | New strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
title_sort | new strategy for designing orangish-red-emitting phosphor via oxygen-vacancy-induced electronic localization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351663/ https://www.ncbi.nlm.nih.gov/pubmed/30728955 http://dx.doi.org/10.1038/s41377-019-0126-1 |
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