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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75375
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dc.contributor.authorNoce, R. D.-
dc.contributor.authorBenedetti, Assis Vicente-
dc.contributor.authorPassamani, E. C.-
dc.contributor.authorKumar, H.-
dc.contributor.authorCornejo, D. R.-
dc.contributor.authorMagnani, M.-
dc.date.accessioned2014-05-27T11:29:29Z-
dc.date.accessioned2016-10-25T18:48:21Z-
dc.date.available2014-05-27T11:29:29Z-
dc.date.available2016-10-25T18:48:21Z-
dc.date.issued2013-05-09-
dc.identifierhttp://dx.doi.org/10.1016/j.jallcom.2013.03.282-
dc.identifier.citationJournal of Alloys and Compounds, v. 573, p. 37-42.-
dc.identifier.issn0925-8388-
dc.identifier.urihttp://hdl.handle.net/11449/75375-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75375-
dc.description.abstractBy combining galvanic displacement and electrodeposition techniques, an ordered Fe20Rh80 structure deposited onto brass was investigated by X-ray diffractometry, Mössbauer spectroscopy and magnetization measurements. Mössbauer and X-ray diffraction analyses suggest that the Fe-Rh alloy directly electrodeposited onto brass displays a nanocrystalline state while a similar alloy deposited onto Ag/brass shows a faced centered cubic-like structure, with dendrites-like features. These results directly indicate that the presence of Ag seed layer is responsible for the Fe-Rh alloy crystallization process. In addition, room temperature Mössbauer data indicate firstly paramagnetic states for two Fe-species. In the dominant Fe-species (major fraction of the Mössbauer spectra), Fe atoms are situated at a cubic environment and it can be attributed to the γ-Fe20Rh80 alloy based on their hyperfine parameters. In the second species, Fe atoms are placed in a non-local symmetry, which can be related to Fe atoms at the grain boundaries or/and Fe small clusters. These Fe-clusters are in superparamagnetic state at room temperature, but they may be ordered below 45 K, as suggested by magnetization data. © 2013 Elsevier B.V. All rights reserved.en
dc.format.extent37-42-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAg seed layer-
dc.subjectElectrodeposition-
dc.subjectFeRh alloys-
dc.subjectGalvanic displacement-
dc.subjectAg seed layers-
dc.subjectElectrochemical techniques-
dc.subjectElectrodeposition technique-
dc.subjectFe-Rh alloy-
dc.subjectMagnetization measurements-
dc.subjectSsbauer spectroscopies-
dc.subjectSuperparamagnetic state-
dc.subjectAtoms-
dc.subjectBrass-
dc.subjectDeposits-
dc.subjectGrain boundaries-
dc.subjectIron alloys-
dc.subjectMagnetization-
dc.subjectMolybdenum-
dc.subjectRhodium-
dc.subjectSilver alloys-
dc.subjectSuperparamagnetism-
dc.subjectX ray diffraction-
dc.subjectX ray diffraction analysis-
dc.subjectNanocrystalline alloys-
dc.titleUse of conventional electrochemical techniques to produce crystalline FeRh alloys induced by Ag seed layeren
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Espírito Santo (UFES)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionCentro Nacional de Pesquisa em Energia e Materiais (CNPEM)-
dc.description.affiliationInstituto de Química Universidade Estadual Paulista UNESP, 14800-900 Araraquara, SP-
dc.description.affiliationDepartamento de Física Universidade Federal Do Espírito Santo, 29075-910 Vitória, ES-
dc.description.affiliationInstituto de Física Universidade de São Paulo USP, 05508-090 São Paulo, SP-
dc.description.affiliationCentro Nacional de Pesquisa em Energia e Materiais (CNPEM), 13083-970 Campinas SP-
dc.description.affiliationUnespInstituto de Química Universidade Estadual Paulista UNESP, 14800-900 Araraquara, SP-
dc.identifier.doi10.1016/j.jallcom.2013.03.282-
dc.identifier.wosWOS:000320585700008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Alloys and Compounds-
dc.identifier.scopus2-s2.0-84877017838-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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