Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1021/acs.jpcc.9b10851 |
Texto Completo: | http://dx.doi.org/10.1021/acs.jpcc.9b10851 http://hdl.handle.net/11449/197322 |
Resumo: | A detailed structural investigation of two series of fluoride phosphate glasses with nominal compositions 20BaF(2)-20SrF(2)-20ZnF(2)-xIn(PO3)(3)-(40 - x)InF3 (x = 0, 5, 10, and 15) and 20BaF(2)-20SrF(2)-20ZnF(2)-10ScF(3)-xIn(PO3)(3)-(30 - x)InF3 (x = 0, 10, 15, 20), both doped with either 0.2 mol % Yb3+ or 0.S mol % Eu3+, has been conducted. As indicated by Raman scattering and solid- state NMR, the network structure is dominated by six-coordinated In3+, orthophosphate Q((0)()) species, and the (near) absence of P-O-P connectivity. The ligand environment of the rare-earth ions is studied by (1) Sc-45 NMR of the diamagnetic mimic Sc3+, (2) echo-detected field-sweep EPR spectra at the X-band, using Yb3+ spin probes, and (3) excitation and emission spectroscopy of Eu3+ dopants. Sc-45{P-31} rotational echo double resonance (REDOR) results, the ratio of the Eu3+ D-5(0) -> F-7(2) to (5) D-0 -> F-7(1) emission intensities, the lifetime values of the Eu3+ emitting level D-5(0), as well as the g factor measured by EPR spectroscopy consistently indicate that the fluoride ligands strongly dominate in the first coordination sphere of the rare-earth ions. This result stands in contrast to previous studies on aluminofluorophosphate glasses with similar compositions that show mixed ligation of the rare-earth ions by fluoride and phosphate ions. Thus, by substituting aluminum by its homologue indium one can achieve the original design goal of fluoride phosphate glasses, which is the creation of a framework structure dominated by oxide, while the local environment of the RE emitting ion is dominated by fluoride ligands, so as to improve their emissive properties. The results also illustrate the successful use of the previously developed combined NMR/EPR/optical characterization strategy for the design of optimized matrices for rare-earth ion emitters. |
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Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical SpectroscopiesA detailed structural investigation of two series of fluoride phosphate glasses with nominal compositions 20BaF(2)-20SrF(2)-20ZnF(2)-xIn(PO3)(3)-(40 - x)InF3 (x = 0, 5, 10, and 15) and 20BaF(2)-20SrF(2)-20ZnF(2)-10ScF(3)-xIn(PO3)(3)-(30 - x)InF3 (x = 0, 10, 15, 20), both doped with either 0.2 mol % Yb3+ or 0.S mol % Eu3+, has been conducted. As indicated by Raman scattering and solid- state NMR, the network structure is dominated by six-coordinated In3+, orthophosphate Q((0)()) species, and the (near) absence of P-O-P connectivity. The ligand environment of the rare-earth ions is studied by (1) Sc-45 NMR of the diamagnetic mimic Sc3+, (2) echo-detected field-sweep EPR spectra at the X-band, using Yb3+ spin probes, and (3) excitation and emission spectroscopy of Eu3+ dopants. Sc-45{P-31} rotational echo double resonance (REDOR) results, the ratio of the Eu3+ D-5(0) -> F-7(2) to (5) D-0 -> F-7(1) emission intensities, the lifetime values of the Eu3+ emitting level D-5(0), as well as the g factor measured by EPR spectroscopy consistently indicate that the fluoride ligands strongly dominate in the first coordination sphere of the rare-earth ions. This result stands in contrast to previous studies on aluminofluorophosphate glasses with similar compositions that show mixed ligation of the rare-earth ions by fluoride and phosphate ions. Thus, by substituting aluminum by its homologue indium one can achieve the original design goal of fluoride phosphate glasses, which is the creation of a framework structure dominated by oxide, while the local environment of the RE emitting ion is dominated by fluoride ligands, so as to improve their emissive properties. The results also illustrate the successful use of the previously developed combined NMR/EPR/optical characterization strategy for the design of optimized matrices for rare-earth ion emitters.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Deutsche ForschungsgemeinschaftUniv Sao Paulo, Inst Fis Sao Carlos, Ave Trabalhador Saocarlense 400, BR-13566590 Sao Carlos, SP, BrazilUniv Estadual Paulista, Inst Quim, Rua Prof Francisco Degni 55, BR-14800060 Araraquara, SP, BrazilWestfalische Wilhelms Univ Munster, Inst Phys Chem, Corrensstr 30, D-48149 Munster, GermanyUniv Estadual Paulista, Inst Quim, Rua Prof Francisco Degni 55, BR-14800060 Araraquara, SP, BrazilFAPESP: 2018/03931-9FAPESP: 2018/24735-3FAPESP: 2017/06649-0CNPq: 406611/2017-3Deutsche Forschungsgemeinschaft: 413550885FAPESP: 2013/07793-6Amer Chemical SocUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Westfalische Wilhelms Univ MunsterGalleani, GustavoDoerenkamp, CarstenSantagneli, Silvia [UNESP]Magon, Claudio JoseCamargo, Andrea S. S. deEckert, Hellmut2020-12-10T20:13:22Z2020-12-10T20:13:22Z2019-12-26info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article31219-31231http://dx.doi.org/10.1021/acs.jpcc.9b10851Journal Of Physical Chemistry C. Washington: Amer Chemical Soc, v. 123, n. 51, p. 31219-31231, 2019.1932-7447http://hdl.handle.net/11449/19732210.1021/acs.jpcc.9b10851WOS:000505632900049Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Physical Chemistry Cinfo:eu-repo/semantics/openAccess2021-10-23T12:39:36Zoai:repositorio.unesp.br:11449/197322Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:04:35.050147Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
title |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
spellingShingle |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies Galleani, Gustavo Galleani, Gustavo |
title_short |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
title_full |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
title_fullStr |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
title_full_unstemmed |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
title_sort |
Compositional Optimization of Emission Properties for Rare-Earth Doped Fluoride Phosphate Glasses: Structural Investigations via NMR, EPR, and Optical Spectroscopies |
author |
Galleani, Gustavo |
author_facet |
Galleani, Gustavo Galleani, Gustavo Doerenkamp, Carsten Santagneli, Silvia [UNESP] Magon, Claudio Jose Camargo, Andrea S. S. de Eckert, Hellmut Doerenkamp, Carsten Santagneli, Silvia [UNESP] Magon, Claudio Jose Camargo, Andrea S. S. de Eckert, Hellmut |
author_role |
author |
author2 |
Doerenkamp, Carsten Santagneli, Silvia [UNESP] Magon, Claudio Jose Camargo, Andrea S. S. de Eckert, Hellmut |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) Westfalische Wilhelms Univ Munster |
dc.contributor.author.fl_str_mv |
Galleani, Gustavo Doerenkamp, Carsten Santagneli, Silvia [UNESP] Magon, Claudio Jose Camargo, Andrea S. S. de Eckert, Hellmut |
description |
A detailed structural investigation of two series of fluoride phosphate glasses with nominal compositions 20BaF(2)-20SrF(2)-20ZnF(2)-xIn(PO3)(3)-(40 - x)InF3 (x = 0, 5, 10, and 15) and 20BaF(2)-20SrF(2)-20ZnF(2)-10ScF(3)-xIn(PO3)(3)-(30 - x)InF3 (x = 0, 10, 15, 20), both doped with either 0.2 mol % Yb3+ or 0.S mol % Eu3+, has been conducted. As indicated by Raman scattering and solid- state NMR, the network structure is dominated by six-coordinated In3+, orthophosphate Q((0)()) species, and the (near) absence of P-O-P connectivity. The ligand environment of the rare-earth ions is studied by (1) Sc-45 NMR of the diamagnetic mimic Sc3+, (2) echo-detected field-sweep EPR spectra at the X-band, using Yb3+ spin probes, and (3) excitation and emission spectroscopy of Eu3+ dopants. Sc-45{P-31} rotational echo double resonance (REDOR) results, the ratio of the Eu3+ D-5(0) -> F-7(2) to (5) D-0 -> F-7(1) emission intensities, the lifetime values of the Eu3+ emitting level D-5(0), as well as the g factor measured by EPR spectroscopy consistently indicate that the fluoride ligands strongly dominate in the first coordination sphere of the rare-earth ions. This result stands in contrast to previous studies on aluminofluorophosphate glasses with similar compositions that show mixed ligation of the rare-earth ions by fluoride and phosphate ions. Thus, by substituting aluminum by its homologue indium one can achieve the original design goal of fluoride phosphate glasses, which is the creation of a framework structure dominated by oxide, while the local environment of the RE emitting ion is dominated by fluoride ligands, so as to improve their emissive properties. The results also illustrate the successful use of the previously developed combined NMR/EPR/optical characterization strategy for the design of optimized matrices for rare-earth ion emitters. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-12-26 2020-12-10T20:13:22Z 2020-12-10T20:13:22Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1021/acs.jpcc.9b10851 Journal Of Physical Chemistry C. Washington: Amer Chemical Soc, v. 123, n. 51, p. 31219-31231, 2019. 1932-7447 http://hdl.handle.net/11449/197322 10.1021/acs.jpcc.9b10851 WOS:000505632900049 |
url |
http://dx.doi.org/10.1021/acs.jpcc.9b10851 http://hdl.handle.net/11449/197322 |
identifier_str_mv |
Journal Of Physical Chemistry C. Washington: Amer Chemical Soc, v. 123, n. 51, p. 31219-31231, 2019. 1932-7447 10.1021/acs.jpcc.9b10851 WOS:000505632900049 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Physical Chemistry C |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
31219-31231 |
dc.publisher.none.fl_str_mv |
Amer Chemical Soc |
publisher.none.fl_str_mv |
Amer Chemical Soc |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1822230015409913856 |
dc.identifier.doi.none.fl_str_mv |
10.1021/acs.jpcc.9b10851 |