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dc.contributor.authorHamdeh, Hussein H.en_US
dc.contributor.authorHikal, W. M.en_US
dc.contributor.authorTaher, S. M.en_US
dc.contributor.authorHo, J. C.en_US
dc.contributor.authorThuy, N. Pen_US
dc.contributor.authorQuy, O. K.; Hanh, N.en_US
dc.date.accessioned2011-12-20T23:52:14Z
dc.date.available2011-12-20T23:52:14Z
dc.date.issued2005-03-01en_US
dc.identifier.citationHamdeh, H. H.; Hikal, W. M.; Taher, S. M.; Ho, J. C.; Thuy, N. P.; Quy, O. K.; Hanh, N.; , "Mössbauer evaluation of cobalt ferrite nanoparticles synthesized by forced hydrolysis," Journal of Applied Physics , vol.97, no.6, pp.064310-064310-4, Mar 2005 doi: 10.1063/1.1856219en_US
dc.identifier.issn0021-8979en_US
dc.identifier.urihttp:dx.doi.org/10.1063/1.1856219en_US
dc.identifier.urihttp://hdl.handle.net/10057/4070
dc.descriptionThe full text of this article is not available on SOAR. WSU users can access the article via IEEE Xplore database licensed by University Libraries: http://libcat.wichita.edu/vwebv/holdingsInfo?bibId=1045955en_US
dc.description.abstractSpinel cobalt ferrite in the form of nearly spherical particles, having a narrow range of particle size around 7.6 nm, was produced by forced hydrolysis. Between the magnetization blocking temperature of 180 K and the Mössbauer blocking temperature of 270 K, the magnetic anisotropy energy decreases rapidly with temperature. The occupancy of the octahedral sites by only half of the Co2+ cations may have weakened the crystalline anisotropy. Significant spin canting was also observed at these sites.en_US
dc.language.isoen_USen_US
dc.publisherIEEEen_US
dc.relation.ispartofseriesJournal of Applied Physics , vol.97, no.6, pp.064310-064310-4en_US
dc.subjectMossbauer effecten_US
dc.subjectCanted spin arrangementsen_US
dc.subjectCobalt compoundsen_US
dc.subjectFerritesen_US
dc.subjectMagnetic anisotropyen_US
dc.subjectMagnetic particlesen_US
dc.subjectMagnetic relaxationen_US
dc.subjectNanoparticlesen_US
dc.subjectParticle sizeen_US
dc.titleMössbauer evaluation of cobalt ferrite nanoparticles synthesized by forced hydrolysisen_US
dc.typeArticleen_US
dc.description.versionPeer reviewed articleen_US
dc.rights.holder© IEEE, 2005en_US


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