Abstract

Yttrium doped barium hexaferrites with chemical composition BaYxFe12−xO19 (0.0≤x≤1.0) were synthesized by facile ceramic route. The effect of the yttrium ion concentration on the temperature-dependent magnetic properties of the BaYxFe12−xO19 hexaferrites (0.0≤x≤1.0) has been investigated in the temperature range of 10–300K and magnetic field of 50kOe. The structural, morphological, compositional and magnetic properties of the products were investigated by using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and vibrating sample magnetometer (VSM) techniques, respectively. XRD patterns demonstrated pure, single phase hexagonal crystal. The average crystallite size of the samples varies in the range of 47–63nm. SEM images indicated hexagonal platelet-like particles. EDX measurements confirmed the expected formula of BaYFe11O19 hexaferrite. It has been observed that the preferential site occupancy of the nonmagnetic yttrium ions strongly changes the magnetic properties. The saturation magnetization value close to the bulk one was measured as 62.62 and 88.21emu/g for 300 and 10K, respectively. It has been found from the magnetization measurements that the saturation magnetization reaches its maximum value at x=0.4 and then decreases with further increasing of the concentration (x). As the temperature goes up, the saturation magnetization decreases due to the weakening of superexchange interaction. The coercive field increases by about three times with increasing of the concentration from x=0.0 to 1.0 due to an increasing of anisotropy field and reaches the maximum value of 3556Oe at x=1.0.

Full Text
Paper version not known

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.