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High Coercivity of Oleic Acid Capped CoFe2O4 Nanoparticles at Room Temperature

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dc.contributor.author Limaye, Mukta V. en_US
dc.contributor.author SINGH, S. en_US
dc.contributor.author Date, S. en_US
dc.contributor.author KULKARNI, SULABHA en_US
dc.date.accessioned 2018-12-06T09:16:34Z
dc.date.available 2018-12-06T09:16:34Z
dc.date.issued 2009-06 en_US
dc.identifier.citation Journal of Physical Chemistry B, 113(27). en_US
dc.identifier.issn 1520-6106 en_US
dc.identifier.issn 1520-5207 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1391
dc.identifier.uri https://doi.org/10.1021/jp810975v en_US
dc.description.abstract High 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Coercivity en_US
dc.subject Oleic Acid Capped CoFe2O4 en_US
dc.subject 2009 en_US
dc.title High Coercivity of Oleic Acid Capped CoFe2O4 Nanoparticles at Room Temperature en_US
dc.type Article en_US
dc.contributor.department Dept. of Physics en_US
dc.identifier.sourcetitle Journal of Physical Chemistry B en_US
dc.publication.originofpublisher Foreign en_US


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