Abstract
This investigation presents the optical, structural, vibrational and magnetic studies of the cubic spinel Fe2+CrFeO4 nano-ferrites, which transformed to maghemite structure by annealed at 250 °C for 3 h and to hexagonal hematite at temperatures T ≥ 500 °C in air. These nanomaterials were synthesized by the co-precipitation route and sintered at different temperatures. A split of the lattice constant a to a and c occurred for T ≥ 500 °C due to the transformation to hexagonal hematite, where c/a ≈ 2.7. The density and trend of crystallite size (R) values showed increase against T, whereas the calculated and experimental specific surface area, threshold energy, Debye temperature and elastic wave velocities showed decrease. The trend of dislocation density, inter-chain distance, distortion parameter, saturation magnetization (Ms), squareness, remnant magnetization, magnetic moment and anisotropy constant was decreased with T. The main IR absorption bands; ν1 and ν2 of the nanomaterials were observed in the IR spectra where their positions proved dependence on T. The porosity (P), strain (ɛ), force constants, elastic and stiffness constants and coercivity revealed dependence on T. Variation of all deduced parameters with T revealed the structure transformation from cubic to hexagonal hematite. The optical band gab energy (Eg) showed increase as T increases. Eg, S and ɛ proved dependence on R, whereas Ms proved dependence on P. So, Dx, Ms and Hc proved effect on the elastic wave velocities.
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.