Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1039/d3ma00053b http://hdl.handle.net/11449/248499 |
Resumo: | Oxide-diluted magnetic semiconductors have received considerable attention in diverse scientific and technological fields because they combine the optoelectronic properties of the hosting semiconductor with the magnetic properties of the metal dopant. In this report, the role of Fe doping on the structural, vibrational, optical, hyperfine, and magnetic properties of Fe-doped ZnO nanoparticles (Zn1−xFexO) synthesized via a polymeric precursor method is presented. Our findings display that the crystallite size decreases from ∼23 nm (x = 0.000) to ∼8 nm (x = 0.200) as the Fe-content (x) is increased. From the XRD data analysis, our results suggest an isovalent solid solution between Fe2+ and Zn2+ ions for lower Fe-content (up to 0.075) and aliovalent solution (Fe3+ and Zn2+ ions) for higher Fe-content. Elliot's theory was used to assess the band gap energy of Eg ∼ 3.4 eV, and an exciton binding energy of Eb ∼ 66 meV for the undoped sample. The excitonic peak exhibits a broadening trend with increasing Fe-content, suggesting disorder enhancement in the ZnO matrix. Besides, FTIR data analysis suggests that the Zn-O bond length increases with Fe-content up to 0.075 and decreases above this value. The intensity ratio of the O-H and Zn-O modes shows a discontinuity as the Fe-content is increased. Room temperature Mössbauer spectra carried out for samples with x = 0.050, 0.075, and 0.200 show that the isomer shift and quadrupole splitting increase with the Fe-content, in agreement with the structural properties. Magnetic measurements suggest that the iron ions stabilize as Fe2+ in samples with low Fe-content and then as Fe3+ in samples with high Fe-content. Besides, the occurrence of short-range antiferromagnetic interactions was determined, which becomes stronger as the Fe-content is increased. |
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Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticlesOxide-diluted magnetic semiconductors have received considerable attention in diverse scientific and technological fields because they combine the optoelectronic properties of the hosting semiconductor with the magnetic properties of the metal dopant. In this report, the role of Fe doping on the structural, vibrational, optical, hyperfine, and magnetic properties of Fe-doped ZnO nanoparticles (Zn1−xFexO) synthesized via a polymeric precursor method is presented. Our findings display that the crystallite size decreases from ∼23 nm (x = 0.000) to ∼8 nm (x = 0.200) as the Fe-content (x) is increased. From the XRD data analysis, our results suggest an isovalent solid solution between Fe2+ and Zn2+ ions for lower Fe-content (up to 0.075) and aliovalent solution (Fe3+ and Zn2+ ions) for higher Fe-content. Elliot's theory was used to assess the band gap energy of Eg ∼ 3.4 eV, and an exciton binding energy of Eb ∼ 66 meV for the undoped sample. The excitonic peak exhibits a broadening trend with increasing Fe-content, suggesting disorder enhancement in the ZnO matrix. Besides, FTIR data analysis suggests that the Zn-O bond length increases with Fe-content up to 0.075 and decreases above this value. The intensity ratio of the O-H and Zn-O modes shows a discontinuity as the Fe-content is increased. Room temperature Mössbauer spectra carried out for samples with x = 0.050, 0.075, and 0.200 show that the isomer shift and quadrupole splitting increase with the Fe-content, in agreement with the structural properties. Magnetic measurements suggest that the iron ions stabilize as Fe2+ in samples with low Fe-content and then as Fe3+ in samples with high Fe-content. Besides, the occurrence of short-range antiferromagnetic interactions was determined, which becomes stronger as the Fe-content is increased.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidad Nacional de San Agustín de Arequipa Av Independencia SNUniversity of Brasília Institute of PhysicsDepartamento de Física Centro de Ciências Exatas e de Tecnologia Universidade Federal de São Carlos, SPInstituto de Física Universidade de São Paulo, SPCatholic University of Brasília Genomic Sciences and Biotechnology, DFPhysics Department IGCE Paulista State University, CEP 13506-900, SPPhysics Department IGCE Paulista State University, CEP 13506-900, SPAv Independencia SNInstitute of PhysicsUniversidade Federal de São Carlos (UFSCar)Universidade de São Paulo (USP)Genomic Sciences and BiotechnologyUniversidade Estadual Paulista (UNESP)Aragón, F. F.H.Villegas-Lelovsky, L. [UNESP]Parizaka, J. G.Zela, E. G.Bendezu, R.Gallegos, R. O.Pacheco-Salazar, D. G.da Silva, S. W.Cohen, R.Nagamine, L. C.C.M.Coaquira, J. A.H.Morais, P. C.2023-07-29T13:45:44Z2023-07-29T13:45:44Z2023-02-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1389-1402http://dx.doi.org/10.1039/d3ma00053bMaterials Advances, v. 4, n. 5, p. 1389-1402, 2023.2633-5409http://hdl.handle.net/11449/24849910.1039/d3ma00053b2-s2.0-85149815545Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMaterials Advancesinfo:eu-repo/semantics/openAccess2023-07-29T13:45:44Zoai:repositorio.unesp.br:11449/248499Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:14:23.958905Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
title |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
spellingShingle |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles Aragón, F. F.H. |
title_short |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
title_full |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
title_fullStr |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
title_full_unstemmed |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
title_sort |
Evidence of progressive Fe2+ to Fe3+oxidation in Fe2+-doped ZnO nanoparticles |
author |
Aragón, F. F.H. |
author_facet |
Aragón, F. F.H. Villegas-Lelovsky, L. [UNESP] Parizaka, J. G. Zela, E. G. Bendezu, R. Gallegos, R. O. Pacheco-Salazar, D. G. da Silva, S. W. Cohen, R. Nagamine, L. C.C.M. Coaquira, J. A.H. Morais, P. C. |
author_role |
author |
author2 |
Villegas-Lelovsky, L. [UNESP] Parizaka, J. G. Zela, E. G. Bendezu, R. Gallegos, R. O. Pacheco-Salazar, D. G. da Silva, S. W. Cohen, R. Nagamine, L. C.C.M. Coaquira, J. A.H. Morais, P. C. |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Av Independencia SN Institute of Physics Universidade Federal de São Carlos (UFSCar) Universidade de São Paulo (USP) Genomic Sciences and Biotechnology Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Aragón, F. F.H. Villegas-Lelovsky, L. [UNESP] Parizaka, J. G. Zela, E. G. Bendezu, R. Gallegos, R. O. Pacheco-Salazar, D. G. da Silva, S. W. Cohen, R. Nagamine, L. C.C.M. Coaquira, J. A.H. Morais, P. C. |
description |
Oxide-diluted magnetic semiconductors have received considerable attention in diverse scientific and technological fields because they combine the optoelectronic properties of the hosting semiconductor with the magnetic properties of the metal dopant. In this report, the role of Fe doping on the structural, vibrational, optical, hyperfine, and magnetic properties of Fe-doped ZnO nanoparticles (Zn1−xFexO) synthesized via a polymeric precursor method is presented. Our findings display that the crystallite size decreases from ∼23 nm (x = 0.000) to ∼8 nm (x = 0.200) as the Fe-content (x) is increased. From the XRD data analysis, our results suggest an isovalent solid solution between Fe2+ and Zn2+ ions for lower Fe-content (up to 0.075) and aliovalent solution (Fe3+ and Zn2+ ions) for higher Fe-content. Elliot's theory was used to assess the band gap energy of Eg ∼ 3.4 eV, and an exciton binding energy of Eb ∼ 66 meV for the undoped sample. The excitonic peak exhibits a broadening trend with increasing Fe-content, suggesting disorder enhancement in the ZnO matrix. Besides, FTIR data analysis suggests that the Zn-O bond length increases with Fe-content up to 0.075 and decreases above this value. The intensity ratio of the O-H and Zn-O modes shows a discontinuity as the Fe-content is increased. Room temperature Mössbauer spectra carried out for samples with x = 0.050, 0.075, and 0.200 show that the isomer shift and quadrupole splitting increase with the Fe-content, in agreement with the structural properties. Magnetic measurements suggest that the iron ions stabilize as Fe2+ in samples with low Fe-content and then as Fe3+ in samples with high Fe-content. Besides, the occurrence of short-range antiferromagnetic interactions was determined, which becomes stronger as the Fe-content is increased. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:45:44Z 2023-07-29T13:45:44Z 2023-02-08 |
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/10.1039/d3ma00053b Materials Advances, v. 4, n. 5, p. 1389-1402, 2023. 2633-5409 http://hdl.handle.net/11449/248499 10.1039/d3ma00053b 2-s2.0-85149815545 |
url |
http://dx.doi.org/10.1039/d3ma00053b http://hdl.handle.net/11449/248499 |
identifier_str_mv |
Materials Advances, v. 4, n. 5, p. 1389-1402, 2023. 2633-5409 10.1039/d3ma00053b 2-s2.0-85149815545 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Materials Advances |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1389-1402 |
dc.source.none.fl_str_mv |
Scopus 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 |
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1808129599076302848 |