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Energy Transfer Processes in NASICON-Type Phosphates under Synchrotron Radiation Excitation
The luminescence properties of NASICON-type Na3.6M1.8(PO4)3 (M = Y, Lu) and Na3Sc2(PO4)3 phosphates, undoped and rare earth-doped (RE = Tb3+, Dy3+, Eu3+, Ce3+), were studied using synchrotron radiation in a wide energy region of 4.5–45 eV. Intrinsic emission originating from self-trapped excitons wi...
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Published in: | Symmetry (Basel) 2023-03, Vol.15 (3), p.749 |
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description | The luminescence properties of NASICON-type Na3.6M1.8(PO4)3 (M = Y, Lu) and Na3Sc2(PO4)3 phosphates, undoped and rare earth-doped (RE = Tb3+, Dy3+, Eu3+, Ce3+), were studied using synchrotron radiation in a wide energy region of 4.5–45 eV. Intrinsic emission originating from self-trapped excitons with electron component localized at the 3d Sc states was detected in both doped and undoped Na3Sc2(PO4)3 while only defect-related emission was registered in Na3.6M1.8(PO4)3. Emission of RE ions substituting three-valent cations in low-symmetry sites was detected in all doped phosphates. The efficiency and pass ways of energy transfer from the host to emission centres were analysed based on luminescence excitation spectra. It is shown that the most efficient energy transfer is realized in Tb3+-doped phosphors, while it was poor for other RE ions. The differences in energy transfer efficiencies are explained by different position of RE f states in the crystal electronic band structure influencing the efficiency of charge carrier trapping in the substance. Based on excitation spectra analysis, the bandgap values were estimated to ~8 eV for all studied phosphates. |
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Intrinsic emission originating from self-trapped excitons with electron component localized at the 3d Sc states was detected in both doped and undoped Na3Sc2(PO4)3 while only defect-related emission was registered in Na3.6M1.8(PO4)3. Emission of RE ions substituting three-valent cations in low-symmetry sites was detected in all doped phosphates. The efficiency and pass ways of energy transfer from the host to emission centres were analysed based on luminescence excitation spectra. It is shown that the most efficient energy transfer is realized in Tb3+-doped phosphors, while it was poor for other RE ions. The differences in energy transfer efficiencies are explained by different position of RE f states in the crystal electronic band structure influencing the efficiency of charge carrier trapping in the substance. Based on excitation spectra analysis, the bandgap values were estimated to ~8 eV for all studied phosphates.</description><identifier>ISSN: 2073-8994</identifier><identifier>EISSN: 2073-8994</identifier><identifier>DOI: 10.3390/sym15030749</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Analysis ; Cerium ; Charge efficiency ; Crystal defects ; Current carriers ; Electron transport ; Emission analysis ; Energy ; Energy transfer ; Excitation spectra ; Excitons ; Luminescence ; NASICON phosphates ; Optical properties ; Phase transitions ; Phosphates ; Phosphors ; Radiation ; Spectrum analysis ; Synchrotron radiation ; Synchrotrons ; Terbium ; X-rays</subject><ispartof>Symmetry (Basel), 2023-03, Vol.15 (3), p.749</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Intrinsic emission originating from self-trapped excitons with electron component localized at the 3d Sc states was detected in both doped and undoped Na3Sc2(PO4)3 while only defect-related emission was registered in Na3.6M1.8(PO4)3. Emission of RE ions substituting three-valent cations in low-symmetry sites was detected in all doped phosphates. The efficiency and pass ways of energy transfer from the host to emission centres were analysed based on luminescence excitation spectra. It is shown that the most efficient energy transfer is realized in Tb3+-doped phosphors, while it was poor for other RE ions. The differences in energy transfer efficiencies are explained by different position of RE f states in the crystal electronic band structure influencing the efficiency of charge carrier trapping in the substance. Based on excitation spectra analysis, the bandgap values were estimated to ~8 eV for all studied phosphates.</description><subject>Analysis</subject><subject>Cerium</subject><subject>Charge efficiency</subject><subject>Crystal defects</subject><subject>Current carriers</subject><subject>Electron transport</subject><subject>Emission analysis</subject><subject>Energy</subject><subject>Energy transfer</subject><subject>Excitation spectra</subject><subject>Excitons</subject><subject>Luminescence</subject><subject>NASICON phosphates</subject><subject>Optical properties</subject><subject>Phase transitions</subject><subject>Phosphates</subject><subject>Phosphors</subject><subject>Radiation</subject><subject>Spectrum analysis</subject><subject>Synchrotron radiation</subject><subject>Synchrotrons</subject><subject>Terbium</subject><subject>X-rays</subject><issn>2073-8994</issn><issn>2073-8994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUU1rGzEQXUILCUlO_QMLOYZNR18r6WiM2xpCEhr31IOQpVlbJpZcaQ3Zf181DiUzh3nMvPcYZprmC4E7xjR8LdOeCGAguT5rLihI1imt-acP-Ly5LmUHNQQI3sNF83sRMW-mdpVtLAPm9iknh6VgaUNsH2bPy_njQ7eaDtg-bVM5bO1YR8foK_V5im6b05hTbH9aH-wYKlq8ujC-wavm82BfCl6_18vm17fFav6ju3_8vpzP7jvHgY2d6h0yrhT6tRyEVj0fGFESwEmCuAbKgHJaq1CMW2m9ohS88D0IJb1n7LJZnnx9sjtzyGFv82SSDeatkfLG2DwG94JGEomge62pQw5CWsqUlmrtiOgHBrZ63Zy8Djn9OWIZzS4dc6zrGyo1kRyIIJV1d2JtbDUNcahHsK6mx31wKeIQan8mBSVcg4IquD0JXE6lZBz-r0nA_Pue-fA99heFwIo5</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Krutyak, Nataliya</creator><creator>Nagirnyi, Vitali</creator><creator>Romet, Ivo</creator><creator>Deyneko, Dina</creator><creator>Spassky, Dmitry</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SC</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><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>H8D</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>JQ2</scope><scope>L6V</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9422-1925</orcidid></search><sort><creationdate>20230301</creationdate><title>Energy Transfer Processes in NASICON-Type Phosphates under Synchrotron Radiation Excitation</title><author>Krutyak, Nataliya ; 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Intrinsic emission originating from self-trapped excitons with electron component localized at the 3d Sc states was detected in both doped and undoped Na3Sc2(PO4)3 while only defect-related emission was registered in Na3.6M1.8(PO4)3. Emission of RE ions substituting three-valent cations in low-symmetry sites was detected in all doped phosphates. The efficiency and pass ways of energy transfer from the host to emission centres were analysed based on luminescence excitation spectra. It is shown that the most efficient energy transfer is realized in Tb3+-doped phosphors, while it was poor for other RE ions. The differences in energy transfer efficiencies are explained by different position of RE f states in the crystal electronic band structure influencing the efficiency of charge carrier trapping in the substance. Based on excitation spectra analysis, the bandgap values were estimated to ~8 eV for all studied phosphates.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/sym15030749</doi><orcidid>https://orcid.org/0000-0002-9422-1925</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Cerium Charge efficiency Crystal defects Current carriers Electron transport Emission analysis Energy Energy transfer Excitation spectra Excitons Luminescence NASICON phosphates Optical properties Phase transitions Phosphates Phosphors Radiation Spectrum analysis Synchrotron radiation Synchrotrons Terbium X-rays |
title | Energy Transfer Processes in NASICON-Type Phosphates under Synchrotron Radiation Excitation |
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