Controlling disorder in the ZnGa\(_2\)O\(_4\):Cr\(^{3+}\) persistent phosphor by Mg\(^{2+}\) substitution
We have studied in this work the effect of increasing structural disorder on the persistent luminescence of Cr\(^{3+}\) doped zinc gallate spinel. This disorder was introduced by progressive substitution of Zn\(^{2+}\) by Mg\(^{2+}\) ions, and was studied by photoluminescence, X-ray diffraction, ext...
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creator | Basavaraju, Neelima Priolkar, Kaustubh R Bessière, Aurélie Sharma, Suchinder K Gourier, Didier Binet, Laurent Viana, Bruno Emura, Shuichi |
description | We have studied in this work the effect of increasing structural disorder on the persistent luminescence of Cr\(^{3+}\) doped zinc gallate spinel. This disorder was introduced by progressive substitution of Zn\(^{2+}\) by Mg\(^{2+}\) ions, and was studied by photoluminescence, X-ray diffraction, extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES) and electron paramagnetic resonance (EPR) spectroscopy. It was found that increasing Mg/Zn substitution decreases the number of Cr\(^{3+}\) in undistorted sites, and increases the number of Cr\(^{3+}\) with neighbouring antisite defects and with neighbouring Cr\(^{3+}\) ions (referred as Cr clusters), which in turn decreases the intensity of persistent luminescence. Both XANES and EPR spectra could be simulated by a linear combination of Cr\(^{3+}\) spectra with three types of Cr\(^{3+}\) environments. The increasing disorder was found to be correlated with a decrease of the average Cr-O bond length and a decrease of crystal field strength experienced by Cr\(^{3+}\) ions. |
doi_str_mv | 10.48550/arxiv.1701.08248 |
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This disorder was introduced by progressive substitution of Zn\(^{2+}\) by Mg\(^{2+}\) ions, and was studied by photoluminescence, X-ray diffraction, extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES) and electron paramagnetic resonance (EPR) spectroscopy. It was found that increasing Mg/Zn substitution decreases the number of Cr\(^{3+}\) in undistorted sites, and increases the number of Cr\(^{3+}\) with neighbouring antisite defects and with neighbouring Cr\(^{3+}\) ions (referred as Cr clusters), which in turn decreases the intensity of persistent luminescence. Both XANES and EPR spectra could be simulated by a linear combination of Cr\(^{3+}\) spectra with three types of Cr\(^{3+}\) environments. The increasing disorder was found to be correlated with a decrease of the average Cr-O bond length and a decrease of crystal field strength experienced by Cr\(^{3+}\) ions.</description><identifier>EISSN: 2331-8422</identifier><identifier>DOI: 10.48550/arxiv.1701.08248</identifier><language>eng</language><publisher>Ithaca: Cornell University Library, arXiv.org</publisher><subject>Antisite defects ; Crystal defects ; Electron paramagnetic resonance ; Field strength ; Fine structure ; Luminescence ; Magnesium ; Phosphors ; Photoluminescence ; Spectrum analysis ; Substitutes ; X ray absorption ; X-ray diffraction ; Zinc</subject><ispartof>arXiv.org, 2017-01</ispartof><rights>2017. This work is published under http://arxiv.org/licenses/nonexclusive-distrib/1.0/ (the “License”). 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This disorder was introduced by progressive substitution of Zn\(^{2+}\) by Mg\(^{2+}\) ions, and was studied by photoluminescence, X-ray diffraction, extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES) and electron paramagnetic resonance (EPR) spectroscopy. It was found that increasing Mg/Zn substitution decreases the number of Cr\(^{3+}\) in undistorted sites, and increases the number of Cr\(^{3+}\) with neighbouring antisite defects and with neighbouring Cr\(^{3+}\) ions (referred as Cr clusters), which in turn decreases the intensity of persistent luminescence. Both XANES and EPR spectra could be simulated by a linear combination of Cr\(^{3+}\) spectra with three types of Cr\(^{3+}\) environments. The increasing disorder was found to be correlated with a decrease of the average Cr-O bond length and a decrease of crystal field strength experienced by Cr\(^{3+}\) ions.</description><subject>Antisite defects</subject><subject>Crystal defects</subject><subject>Electron paramagnetic resonance</subject><subject>Field strength</subject><subject>Fine structure</subject><subject>Luminescence</subject><subject>Magnesium</subject><subject>Phosphors</subject><subject>Photoluminescence</subject><subject>Spectrum analysis</subject><subject>Substitutes</subject><subject>X ray absorption</subject><subject>X-ray diffraction</subject><subject>Zinc</subject><issn>2331-8422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNysFKw0AUheFBEFq0D9DdgJsGaby5M2Oi26DtRty4ksGQ0rGdEmbivRNRxHc3Fh_AxeFfnE-IeQG5royBq5Y-_HtelFDkUKGuTsQUlSqWlUaciBnzAQDwukRj1FT4OoZEset82Mmt50hbR9IHmfZOPodVaxcN2uxxjLbZbU128fKlLr9tJntH7Dm5kGS_jzyO5OZTPux-CR4JDxtOPg3Jx3AuTl_bjt3sr2fi4v7uqV4ve4pvg-PUHOJAYbwahFKbGwSl1f_UD1mGTHQ</recordid><startdate>20170128</startdate><enddate>20170128</enddate><creator>Basavaraju, Neelima</creator><creator>Priolkar, Kaustubh R</creator><creator>Bessière, Aurélie</creator><creator>Sharma, Suchinder K</creator><creator>Gourier, Didier</creator><creator>Binet, Laurent</creator><creator>Viana, Bruno</creator><creator>Emura, Shuichi</creator><general>Cornell University Library, arXiv.org</general><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope></search><sort><creationdate>20170128</creationdate><title>Controlling disorder in the ZnGa\(_2\)O\(_4\):Cr\(^{3+}\) persistent phosphor by Mg\(^{2+}\) substitution</title><author>Basavaraju, Neelima ; 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This disorder was introduced by progressive substitution of Zn\(^{2+}\) by Mg\(^{2+}\) ions, and was studied by photoluminescence, X-ray diffraction, extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES) and electron paramagnetic resonance (EPR) spectroscopy. It was found that increasing Mg/Zn substitution decreases the number of Cr\(^{3+}\) in undistorted sites, and increases the number of Cr\(^{3+}\) with neighbouring antisite defects and with neighbouring Cr\(^{3+}\) ions (referred as Cr clusters), which in turn decreases the intensity of persistent luminescence. Both XANES and EPR spectra could be simulated by a linear combination of Cr\(^{3+}\) spectra with three types of Cr\(^{3+}\) environments. The increasing disorder was found to be correlated with a decrease of the average Cr-O bond length and a decrease of crystal field strength experienced by Cr\(^{3+}\) ions.</abstract><cop>Ithaca</cop><pub>Cornell University Library, arXiv.org</pub><doi>10.48550/arxiv.1701.08248</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antisite defects Crystal defects Electron paramagnetic resonance Field strength Fine structure Luminescence Magnesium Phosphors Photoluminescence Spectrum analysis Substitutes X ray absorption X-ray diffraction Zinc |
title | Controlling disorder in the ZnGa\(_2\)O\(_4\):Cr\(^{3+}\) persistent phosphor by Mg\(^{2+}\) substitution |
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