Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1391
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dc.contributor.authorLimaye, Mukta V.en_US
dc.contributor.authorSINGH, S.en_US
dc.contributor.authorDate, S.en_US
dc.contributor.authorKULKARNI, SULABHAen_US
dc.date.accessioned2018-12-06T09:16:34Z
dc.date.available2018-12-06T09:16:34Z
dc.date.issued2009-06en_US
dc.identifier.citationJournal of Physical Chemistry B, 113(27).en_US
dc.identifier.issn1520-6106en_US
dc.identifier.issn1520-5207en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1391-
dc.identifier.urihttps://doi.org/10.1021/jp810975ven_US
dc.description.abstractHigh coercivity (9.47 kOe) has been obtained for oleic acid capped chemically synthesized CoFe2O4 nanoparticles of crystallite size ∼20 nm. X-ray diffraction analysis confirms the formation of spinel phase in these nanoparticles. Thermal annealing at various temperatures increases the particle size and ultimately shows bulk like properties at particle size ∼56 nm. The nature of bonding of oleic acid with CoFe2O4 nanoparticles and amount of oleic acid in the sample is determined by Fourier transform infrared spectroscopy and thermogrvimetric analysis, respectively. The Raman analysis suggests that the samples are under strain due to capping molecules. Cation distribution in the sample is studied using Mössbauer spectroscopy. Oleic acid concentration dependent studies show that the amount of capping molecules plays an important role in achieving such a high coercivity. On the basis of above observations, it has been proposed that very high coercivity (9.47 kOe) is the result of the magnetic anisotropy, strain, and disorder of the surface spins developed by covalently bonded oleic acid to the surface of CoFe2O4 nanoparticles.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCoercivityen_US
dc.subjectOleic Acid Capped CoFe2O4en_US
dc.subject2009en_US
dc.titleHigh Coercivity of Oleic Acid Capped CoFe2O4 Nanoparticles at Room Temperatureen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.sourcetitleJournal of Physical Chemistry Ben_US
dc.publication.originofpublisherForeignen_US
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