Synthesis, structural, magnetic and electrical properties of Co 1-xZnxFe2O4 (x = 0.0, 0.2) nanoparticles
2013 (English)In: Materials research bulletin, ISSN 0025-5408, E-ISSN 1873-4227, Vol. 48, no 2, 646-654 p.Article in journal (Refereed) Published
Co1-xZnxFe2O4 spinel nanoparticles with Zn concentrations of x = 0.0, 0.2 were prepared by a hydrothermal route in the presence of triethylene glycol (TEG). The structural, magnetic, electrical and dielectric properties of the prepared nanoparticles were studied. The XRD results confirmed the formation of single spinel ferrite structure with crystallite size 9 and 10 nm for x = 0.0 and 0.2 compositions respectively. The lattice parameter (a) increased with increasing Zn concentration. Temperature and frequency dependent electrical and dielectric properties of the prepared ferrites have also been investigated. Our findings show that overall conductivity of Co0.8Zn0.2Fe 2O4 nanoparticle is lower than that of CoFe 2O4 and roughly in the range of 10-11-10 -7 S cm-1 depending strongly temperature and frequency owing to the formation of stable electric bonds between the Zn2+ and Fe2+ ions, which localizes Fe2+ charge carriers. The ac conductivity showed a temperature dependent behavior at low frequencies and temperature independent behavior at high frequencies, which is an indication of ionic conductivity. dc conductivity of Co0.8Zn0.2Fe 2O4 nanoparticle are found to obey the Arrhenius plot and can be classified into two regions over with activation energy of 0.113 and 0.163 eV in the ranges of 20-40 °C and 70-120 °C, respectively when CoFe2O4 has an activation energy of 0.245 eV.
Place, publisher, year, edition, pages
2013. Vol. 48, no 2, 646-654 p.
A. Magnetic materials, A. Structural materials, B. Chemical synthesis, C. Impedance spectroscopy, D. Electrical properties
Engineering and Technology
IdentifiersURN: urn:nbn:se:kth:diva-118305DOI: 10.1016/j.materresbull.2012.11.032ISI: 000315751300076ScopusID: 2-s2.0-84871721888OAI: oai:DiVA.org:kth-118305DiVA: diva2:605713
QC 201302152013-02-152013-02-142013-04-04Bibliographically approved