Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/9592 |
Resumo: | The search for materials with a high degree of purity and crystallization will impact the technological industrial era due to the various applications. However, it is important to look for synthetic methods that are more economical and efficient. In this sense, Ca(0.5)Sr(0.5)MoO4 crystals were synthesized by the coprecipitation method and processed in a hydrothermal microwave oven using different solvent ratios (H2O/C2H6O2), in order to obtain the crystals with high degree of crystallization. The synthesized crystals were characterized by X-ray powder diffraction, lattice parameters, ultraviolet-visible spectroscopy and photoluminescence measurements. The X-ray patterns showed that the crystals have a long-range structural organization, free of secondary phase. The network parameters of the unit cell obtained in this work are very close to the respective values of the JCPDS file nº 30-1287, with some variations that may be related to the synthesis method. The measurements of UV-vis absorption showed the values of the optical band gap as a function of the proportions of solvents ranging from 3.92 to 4.26 eV. The photoluminescence spectra showed broadband with maximum emissions ranging from blue to green. Finally, Ca(0.5)Sr(0.5) MoO4 can be successfully obtained by the methodology used and the use of different proportions of solvents (H2O/C2H6O2) interferes with the optical behavior of the material. |
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Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent studySíntesis de cristales de Ca(0,5)Sr(0,5)MoO4 vía método de coprecipitación y procesamiento en horno hidrotérmico de microondas: estudio estructural y fotoluminiscenteSíntese de cristais de Ca(0,5)Sr(0,5)MoO4 via método de coprecipitação e processamento em forno micro-ondas hidrotermal: estudo estrutural e fotoluminescenteMolibdatoSolventesFotoluminescência.MolibdatoSolventesFotoluminiscencia.MolybdateSolventsPhotoluminescence.The search for materials with a high degree of purity and crystallization will impact the technological industrial era due to the various applications. However, it is important to look for synthetic methods that are more economical and efficient. In this sense, Ca(0.5)Sr(0.5)MoO4 crystals were synthesized by the coprecipitation method and processed in a hydrothermal microwave oven using different solvent ratios (H2O/C2H6O2), in order to obtain the crystals with high degree of crystallization. The synthesized crystals were characterized by X-ray powder diffraction, lattice parameters, ultraviolet-visible spectroscopy and photoluminescence measurements. The X-ray patterns showed that the crystals have a long-range structural organization, free of secondary phase. The network parameters of the unit cell obtained in this work are very close to the respective values of the JCPDS file nº 30-1287, with some variations that may be related to the synthesis method. The measurements of UV-vis absorption showed the values of the optical band gap as a function of the proportions of solvents ranging from 3.92 to 4.26 eV. The photoluminescence spectra showed broadband with maximum emissions ranging from blue to green. Finally, Ca(0.5)Sr(0.5) MoO4 can be successfully obtained by the methodology used and the use of different proportions of solvents (H2O/C2H6O2) interferes with the optical behavior of the material.La búsqueda de materiales con un alto grado de pureza y cristalización impactará en la era tecnológica industrial debido a las diversas aplicaciones. Sin embargo, es importante buscar métodos sintéticos que sean más económicos y eficientes. En este sentido, los cristales de Ca(0,5)Sr(0,5)MoO4 fueron sintetizados por el método de coprecipitación y procesados en un horno de microondas hidrotermal utilizando diferentes proporciones de solventes (H2O/C2H6O2), con el fin de obtener cristales con un alto grado de cristalización. Los cristales sintetizados fueron caracterizados por difracción de rayos X de polvo, parámetros de red, espectroscopía ultravioleta visible y mediciones de fotoluminiscencia. Los patrones de rayos X mostraron que los cristales tienen una organización estructural de largo alcance, libre de fase secundaria. Los parámetros de red de la celda unitaria obtenidos en este trabajo están muy próximos a los valores respectivos del archivo JCPDS nº 30-1287, con algunas variaciones que pueden estar relacionadas con el método de síntesis. Las medidas de absorción UV-vis mostraron los valores de “band gap” óptico en función de las proporciones de disolventes que van desde 3,92 a 4,26 eV. Los espectros de fotoluminiscencia mostraron banda ancha con emisiones máximas que van del azul al verde. Finalmente Ca(0,5)Sr(0,5)MoO4 se puede obtener con éxito mediante la metodología utilizada y el uso de diferentes proporciones de solventes (H2O/C2H6O2) interfiere con el comportamiento óptico del material.A busca por materiais com alto grau de pureza e cristalização causará impacto na era industrial tecnológica devido às diversas aplicações. No entanto, é importante procurar métodos sintéticos que sejam mais econômicos e eficientes. Nesse sentido, cristais de Ca(0,5)Sr(0,5)MoO4 foram sintetizados pelo método de coprecipitação e processados em forno de micro-ondas hidrotermal utilizando diferentes proporções de solventes (H2O/C2H6O2), a fim de obter os cristais com alto grau de cristalização. Os cristais sintetizados foram caracterizados por difração de pó de raios-X, parâmetros de rede, espectroscopia ultravioleta-visível e medidas de fotoluminescência. Os padrões de raios X mostraram que os cristais têm uma organização estrutural de longo alcance, livre de fase secundária. Os parâmetros de rede da célula unitária obtidos neste trabalho estão muito próximos dos respectivos valores da ficha JCPDS nº 30-1287, existindo algumas variações que podem estar relacionadas com o método de síntese. As medições de absorção de UV- vis mostraram os valores de “band gap” óptico em função das proporções de solventes variando de 3,92 a 4,26 eV. Os espectros de fotoluminescência apresentaram banda larga com emissões máximas variando de azul a verde. Enfim, o Ca(0,5)Sr(0,5)MoO4 pode ser obtido com sucesso pela metodologia usada, e o uso de diferentes proporções de solventes (H2O/C2H6O2) interfere no comportamento óptico do material.Research, Society and Development2020-11-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/959210.33448/rsd-v9i11.9592Research, Society and Development; Vol. 9 No. 11; e679119592Research, Society and Development; Vol. 9 Núm. 11; e679119592Research, Society and Development; v. 9 n. 11; e6791195922525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/9592/8539Copyright (c) 2020 Francisco de Assis Sales Ribeiro; Marinaldo Matias da Silva Junior; Cybelle Rodrigues Duarte; Renato César da Silva; Vicente de Sousa Marqueshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessRibeiro, Francisco de Assis Sales Silva Junior, Marinaldo Matias daDuarte, Cybelle RodriguesSilva, Renato César da Marques, Vicente de Sousa2020-12-10T23:37:57Zoai:ojs.pkp.sfu.ca:article/9592Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:31:49.872941Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study Síntesis de cristales de Ca(0,5)Sr(0,5)MoO4 vía método de coprecipitación y procesamiento en horno hidrotérmico de microondas: estudio estructural y fotoluminiscente Síntese de cristais de Ca(0,5)Sr(0,5)MoO4 via método de coprecipitação e processamento em forno micro-ondas hidrotermal: estudo estrutural e fotoluminescente |
title |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
spellingShingle |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study Ribeiro, Francisco de Assis Sales Molibdato Solventes Fotoluminescência. Molibdato Solventes Fotoluminiscencia. Molybdate Solvents Photoluminescence. |
title_short |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
title_full |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
title_fullStr |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
title_full_unstemmed |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
title_sort |
Synthesis of crystals of Ca(0,5)Sr(0,5)MoO4 via method of coprecipitation and processing in a hydrothermal microwaves oven: structural and photoluminescent study |
author |
Ribeiro, Francisco de Assis Sales |
author_facet |
Ribeiro, Francisco de Assis Sales Silva Junior, Marinaldo Matias da Duarte, Cybelle Rodrigues Silva, Renato César da Marques, Vicente de Sousa |
author_role |
author |
author2 |
Silva Junior, Marinaldo Matias da Duarte, Cybelle Rodrigues Silva, Renato César da Marques, Vicente de Sousa |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Ribeiro, Francisco de Assis Sales Silva Junior, Marinaldo Matias da Duarte, Cybelle Rodrigues Silva, Renato César da Marques, Vicente de Sousa |
dc.subject.por.fl_str_mv |
Molibdato Solventes Fotoluminescência. Molibdato Solventes Fotoluminiscencia. Molybdate Solvents Photoluminescence. |
topic |
Molibdato Solventes Fotoluminescência. Molibdato Solventes Fotoluminiscencia. Molybdate Solvents Photoluminescence. |
description |
The search for materials with a high degree of purity and crystallization will impact the technological industrial era due to the various applications. However, it is important to look for synthetic methods that are more economical and efficient. In this sense, Ca(0.5)Sr(0.5)MoO4 crystals were synthesized by the coprecipitation method and processed in a hydrothermal microwave oven using different solvent ratios (H2O/C2H6O2), in order to obtain the crystals with high degree of crystallization. The synthesized crystals were characterized by X-ray powder diffraction, lattice parameters, ultraviolet-visible spectroscopy and photoluminescence measurements. The X-ray patterns showed that the crystals have a long-range structural organization, free of secondary phase. The network parameters of the unit cell obtained in this work are very close to the respective values of the JCPDS file nº 30-1287, with some variations that may be related to the synthesis method. The measurements of UV-vis absorption showed the values of the optical band gap as a function of the proportions of solvents ranging from 3.92 to 4.26 eV. The photoluminescence spectra showed broadband with maximum emissions ranging from blue to green. Finally, Ca(0.5)Sr(0.5) MoO4 can be successfully obtained by the methodology used and the use of different proportions of solvents (H2O/C2H6O2) interferes with the optical behavior of the material. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-11-04 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/9592 10.33448/rsd-v9i11.9592 |
url |
https://rsdjournal.org/index.php/rsd/article/view/9592 |
identifier_str_mv |
10.33448/rsd-v9i11.9592 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/9592/8539 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 9 No. 11; e679119592 Research, Society and Development; Vol. 9 Núm. 11; e679119592 Research, Society and Development; v. 9 n. 11; e679119592 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052662696378368 |