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Electron paramagnetic resonance, magnetic and electrical properties of CoFe2O4 nanoparticles
CoFe2O4 nanoparticles were prepared by solution combustion method. The nanoparticle are characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy and scanning electron microscopy (SEM). PXRD reveals single phase, cubic spinel structure with Fd3¯m (227) space group. SE...
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Published in: | Journal of magnetism and magnetic materials 2013-08, Vol.339, p.40-45 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | CoFe2O4 nanoparticles were prepared by solution combustion method. The nanoparticle are characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy and scanning electron microscopy (SEM). PXRD reveals single phase, cubic spinel structure with Fd3¯m (227) space group. SEM micrograph shows the particles are agglomerated and porous in nature. Electron paramagnetic resonance spectrum exhibits a broad resonance signal g=2.150 and is attributed to super exchange between Fe3+ and Co2+. Magnetization values of CoFe2O4 nanoparticle are lower when compared to the literature values of bulk samples. This can be attributed to the surface spin canting due to large surface-to-volume ratio for a nanoscale system. The variation of dielectric constant, dielectric loss, loss tangent and AC conductivity of as-synthesized nano CoFe2O4 particles at room temperature as a function of frequency has been studied. The magnetic and dielectric properties of the samples show that they are suitable for electronic and biomedical applications.
► CoFe2O4 magnetic nanopowder has been prepared at much lower temperature. ► Sample is well characterized by PXRD, SEM and FTIR spectroscopy. ► Magnetic, electrical and dielectric properties were reported. ► EPR and magnetic properties were correlated to compare the magneto anisotropy. |
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ISSN: | 0304-8853 |
DOI: | 10.1016/j.jmmm.2013.02.028 |