Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/12583
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dc.contributor.authorAntić, Borisen
dc.contributor.authorJovic N.en
dc.contributor.authorPavlovic M.en
dc.contributor.authorKremenovic A.en
dc.contributor.authorManojlović, Draganen
dc.contributor.authorVučinić-Vasić, Milicaen
dc.contributor.authorNikolić A.en
dc.date.accessioned2020-03-03T14:49:04Z-
dc.date.available2020-03-03T14:49:04Z-
dc.date.issued2010-03-15en
dc.identifier.issn218979en
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/12583-
dc.description.abstractIn this paper we report results of structural, spectroscopic, and magnetic investigations of MgFe2O4 nanoparticles prepared by soft mechanochemical synthesis. MgFe2O4 nanoparticles crystallize in Fd̄3m space group with mixed cation distribution and reduced percentage of Fe3+ at tetrahedral (8a) sites. Discrepancy in the cation distribution compared to that in the bulk Mg-ferrite is one of the highest known. X-ray line broadening analysis reveals crystallite size and strain anisotropy. The saturation magnetization, Msat =62 emu/g measured at 5 K is twice higher than that found in the bulk counterparts. Such high value of Msat is attributed to the low value of cation inversion parameter (δ=0.69), to the core/shell structure of the nanoparticles and to the surface/volume ratio. Mössbauer spectrum collected at room temperature reveals ferrimagnetic ordering between Fe3+ ions in 8a and 16d sites, while zero-field-cooled (ZFC) and field-cooled (FC) M(T) measurements were shown superparamagnetic state above 350 K. © 2010 American Institute of Physics.en
dc.relation.ispartofJournal of Applied Physicsen
dc.titleMagnetization enhancement in nanostructured random type MgFe <inf>2</inf>O<inf>4</inf> spinel prepared by soft mechanochemical routeen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.1063/1.3319563en
dc.identifier.scopus2-s2.0-77749301713en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/77749301713en
dc.relation.issue4en
dc.relation.volume107en
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFakultet tehničkih nauka, Departman za energetiku, elektroniku i telekomunikacije-
crisitem.author.deptFakultet tehničkih nauka, Departman za građevinarstvo i geodeziju-
crisitem.author.deptFakultet tehničkih nauka, Departman za opšte discipline u tehnici-
crisitem.author.parentorgFakultet tehničkih nauka-
crisitem.author.parentorgFakultet tehničkih nauka-
crisitem.author.parentorgFakultet tehničkih nauka-
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