Abstract
Using the solid-phase reaction method we obtained bismuth ferrite based compounds generated by partial substitution of bismuth ions with rare earth metal ions (lanthanum and praseodymium). We used thermogravimetric analysis and X-ray analysis at the temperature range from 297 to 1123 K to study the peculiarities of the processes of phase formation of reaction-products synthesis in the systems which contain oxides of iron, bismuth, lanthanum, and praseodymium; their compositions were also determined. For the final synthesis temperature of 1123 K we determined a homogeneous concentration area, where bismuth ferrite solid solutions with the structure of distorted perovskite exist. We studied the influence of lanthanum and praseodymium oxides on phase composition of bismuth ferrite compounds in the process of isovalent alloying of a part of bismuth ions by lanthanum and praseodymium ions. In the frequency range of 20 Hz – 1 MHz we determined the key parameters, which characterize electrical and magnetic properties of perovskite-like phases. We found that for the considered samples the frequency dependencies of complex magnetic permeability and electrical parameters (real and alleged part of permittivity) are of almost the same type. We showed that for the given frequency range both electrical (complex permittivity) and magnetic (complex magnetic permeability) parameters decrease with the frequency increase
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Bulletin of the South Ural State University series "Mathematics. Mechanics. Physics"
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.