Co-precipitation synthesis of Co2+xFe2+1-xFe2O4nanoparticles: Structural characterization and magnetic properties

Cobalt ferrite is known as a promising magnetic material for various applications. This metal-ceramic composite (Cox2+Fe1-x2+Fe2O4) was synthesized via co-precipitation route, by varying the Co/Fe ratios (Co/Fe = 0.3, 0.2, and 0). The structures and magnetic properties of nano-composites were analyz...

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Main Authors: Soleimani, H., Yahya, N., Latiff, N.R.A., Sabet, M., Guan, B.H., Chuan, L.K.
Format: Conference or Workshop Item
Institution: Universiti Teknologi Petronas
Record Id / ISBN-0: utp-eprints.31108 /
Published: American Institute of Physics Inc. 2014
Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969796301&doi=10.1063%2f1.4898514&partnerID=40&md5=f5a9461569870fc391942045b7af90fb
http://eprints.utp.edu.my/31108/
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Summary: Cobalt ferrite is known as a promising magnetic material for various applications. This metal-ceramic composite (Cox2+Fe1-x2+Fe2O4) was synthesized via co-precipitation route, by varying the Co/Fe ratios (Co/Fe = 0.3, 0.2, and 0). The structures and magnetic properties of nano-composites were analyzed by XRD and VSM. As deduced from the XRD line broadening, the average crystallite size of the samples was found to be in the range of 13.0-15.0 nm and contain fcc structure with smaller lattice constant as the Co/Fe ratios increases. FESEM and TEM images revealed the morphology of the samples, which consist of irregular shapes of diameter in the range of 9.0-15.0 nm. Magnetic properties measurement shows that sample S11 with the highest Co/Fe ratio has the highest value of saturation magnetization (Ms) of 65.23 emu/g. On the other hand, increase in the concentration of cobalt ions improves the remanence magnetization (Mr) and coercivity (Hc) of the same sample to 12.18 emu/g and 238.92 Oe, respectively. It is demonstrated that the higher substitution ratio of cobalt in Cox2+Fe1-x2+Fe2O4 has successfully improve the magnetic properties of the samples. © 2014 AIP Publishing LLC.