Abstract

Al3Fe5O12 (AIG) nanopowders were synthesized at different pH using aqueous co-precipitation method. The effect of pH on the phase formation of AIG is characterized using XRD, TEM and TG/DTA. From Scherrer formula the average crystallite sizes were found to be 20, 25, 28 and 32 nm for pH 9, 10, 11 and 12. From TEM micrographs, the particle sizes of the powders were found to be 15, 21, 25 and 30 nm for pH 9, 10, 11 and 12, respectively. It is found that as the pH of the solution increase the particle size also increases. It is clear from the TG/DTA curves that as the pH is increasing the weight losses were found to be small. The obtained nanopowders were further sintered at 900 °C/4 h using conventional sintering method. The phase formation is completed at 800 °C which is correlated with TG/DTA. X-ray photoelectron spectroscopy is used to study the electronic state of the AIG sample. The average grain size of the samples is found to be ~55 nm. Room temperature magnetization measurements established these compounds to be soft magnetic. The room temperature dielectric and magnetic properties (e′, e″, µ′ and µ″) of AIG was studied over a wide range of frequency 1 MHz–1.8 GHz. The dielectric constant was found to decrease with increasing frequency. With increase of pH both e′ and µ′ increased. The Curie temperature was confirmed to be from 560 K (~287 °C) based on the dielectric anomaly observed when these measurements were carried out over a temperature range of 300–600 K. The ferromagnetic resonance linewidth is found to be increasing from 77 to 142 Oe and the effective saturation magnetization (4πMeff) is found to be higher compare to effective saturation magnetization (4πMs) by VSM. This finding provides a new route for AIG materials could be useful for various applications for spintronics.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.