Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/6294
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dc.contributor.authorPereira, A. S.pt
dc.contributor.authorAnkiewicz, A. O.pt
dc.contributor.authorGehlhoff, W.pt
dc.contributor.authorHoffmann, A.pt
dc.contributor.authorPereira, S.pt
dc.contributor.authorTrindade, T.pt
dc.contributor.authorGrundmann, M.pt
dc.contributor.authorCarmo, M. C.pt
dc.contributor.authorSobolev, N. A.pt
dc.date.accessioned2012-02-13T18:02:29Z-
dc.date.available2012-02-13T18:02:29Z-
dc.date.issued2008-
dc.identifier.issn0021-8979pt
dc.identifier.urihttp://hdl.handle.net/10773/6294-
dc.description.abstractA series of chemically prepared Co2+-doped ZnO colloids has been surface modified either by growing shells of ZnSe or by the in situ encapsulation in poly styrene . The surface modification effects using these two distinct chemical strategies on the magnetic properties of the nanocrystals were probed by electron paramagnetic resonance EPR . Structural characterization by means of x-ray diffraction and transmission electron microscopy gave no evidence of second phase formation within the detection limits of the used equipment. The EPR analysis was carried out by simulations of the powderlike EPR spectra. The results confirm that in the core of these nanocrystals Co was incorporated as Co2+, occupying the Zn2+ sites in the wurtzite structure of ZnO. Additionally we identify two Co signals stemming from the nanocrystals’ shell. The performed surface modifications clearly change the relative intensity of the EPR spectrum components, revealing the core and shell signals.pt
dc.language.isoengpt
dc.publisherAmerican Institute of Physicspt
dc.rightsopenAccesspor
dc.titleSurface modification of Co-doped ZnO nanocrystals and its effects on the magnetic propertiespt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage1pt
degois.publication.issue7pt
degois.publication.issue7
degois.publication.lastPage3pt
degois.publication.titleJournal Of Applied Physicspt
degois.publication.volume103pt
dc.identifier.doi10.1063/1.2833300*
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