Abstract
Nanopowders of MnxZn1−xFe2O4 with x=0.4, 0.5 and 0.6 were synthesized using a combustion synthesis method. X-ray diffraction (XRD) patterns obtained on samples confirmed formation of monophasic cubic phase material. Lattice parameters and X-ray densities were obtained from rietvield refinement of the XRD patterns. All samples were radiated with gamma radiation with a dose of 200Gy obtained from 60Co source. Structural and physical parameters, such as lattice constant, X-ray density and particle size, determined for as prepared samples (SA) and gamma irradiated samples (SR), showed extraordinary variations in their values. Saturation magnetizations (MS), remnant magnetization (MR) and coercive field (HC) for both sets of samples illustrated an enhancement in their values for SR samples. Investigations were carried out using Mössbauer spectroscopy to divulge structural and magnetic information of all samples. Room temperature Mössbauer spectra were fitted with five magnetic sextets and a symmetric paramagnetic doublet for the data obtained on samples except for x=0.4, SA sample. The presence of well defined doublets in the spectra of SA and SR samples is attributes of superparamagnetism, indicating the reduction in A–B superexchange interaction due to dilution of sub-lattice by Zn ions. Cation distribution at A site and B site, estimated from Mössbauer data exhibited amazing alterations which were highly stable. The variations in physical, structural and magnetic properties observed are attributed to change of Fe2+/Fe3+ and Mn+2/Mn+3 ratios in gamma-irradiated samples.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.