Magnetic, ferroelectric, and magnetodielectric properties of BiFeO3 ceramic co-doped with Eu and Gd

Polycrystalline samples of Bi0.9Eu0.1FeO3, Bi0.9Gd0.1FeO3, and Bi0.9Eu0.05Gd0.05FeO3 ceramics were synthesized by a solid-state reaction method, followed by rapid quenching to room temperature. Bi0.9Eu0.1FeO3 shows higher magnetization than Bi0.9Gd0.1FeO3 and Bi0.9Eu0.05Gd0.05FeO3. This can be expla...

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Published inThe Journal of physics and chemistry of solids Vol. 124; pp. 19 - 23
Main Authors Kumar, Amit, Yadav, K.L., Kumar, Sonu, Kumar, Naveen, Mishra, Anupam, Shankar, Uma, Mehrotra, Tarang, Sharma, Gyaneshwar, Kumar, Rajendra, Adhikary, Gobinda Das
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.01.2019
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Summary:Polycrystalline samples of Bi0.9Eu0.1FeO3, Bi0.9Gd0.1FeO3, and Bi0.9Eu0.05Gd0.05FeO3 ceramics were synthesized by a solid-state reaction method, followed by rapid quenching to room temperature. Bi0.9Eu0.1FeO3 shows higher magnetization than Bi0.9Gd0.1FeO3 and Bi0.9Eu0.05Gd0.05FeO3. This can be explained by lattice distortion, and the change in the statistical distribution of Fe3+/Fe2+. Similarly, ferroelectric polarization of Bi0.9Eu0.1FeO3 was found to be higher than that of Bi0.9Gd0.1FeO3 and Bi0.9Eu0.05Gd0.05FeO3. However, the absolute value of the magnetocapacitance of Bi0.9Eu0.05Gd0.05FeO3 (∼1.6%) was found to be higher than that of Bi0.9Eu0.1FeO3 (∼1.3%) and Bi0.9 Gd 0.1FeO3 (∼1.1%). In addition, the quadratic component of magnetoelectric coupling is higher for Bi0.9Eu0.05Gd0.05FeO3, which makes Bi0.9Eu0.05Gd0.05FeO3 attractive for further study. •The dielectric constant at room temperature of sample-3 was found to be higher than that of samples-1 and 2.•The magnetization of sample-3 was found to be greater than that of samples-1 and 2.•The polarization–electric field loop of sample-3 was found to be better than that of samples-1 and 2.•The absolute value of the magnetocapacitance of sample-2 was found to be higher than that of samples-1 and 3.
ISSN:0022-3697
1879-2553
DOI:10.1016/j.jpcs.2018.08.037