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Dielectric and polarization studies of magnetoelectric coupling in non-relaxor Pb(Fe.sub.1/2./sub.Ta.sub.1/2./sub.)O.sub.3./sub. multiferroic ceramics
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SYSNO ASEP 0474905 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Dielectric and polarization studies of magnetoelectric coupling in non-relaxor Pb(Fe1/2Ta1/2)O3 multiferroic ceramics Author(s) Savinov, Maxim (FZU-D) RID, ORCID
Bednyakov, Petr (FZU-D) RID, ORCID
Raevskaya, S. I. (RU)
Gusev, A.A. (RU)
Isupov, V.P. (RU)
Raevski, I. P. (RU)
Titov, V.V. (RU)
Chen, H. (CN)
Kovrigina, S.A. (RU)
Chou, C.-C. (TW)
Minasyan, T.A. (RU)
Malitskaya, M. A. (RU)Number of authors 12 Source Title Ferroelectrics. - : Taylor & Francis - ISSN 0015-0193
Roč. 509, č. 1 (2017), s. 80-91Number of pages 12 s. Language eng - English Country GB - United Kingdom Keywords lead iron tantalate ; PFT ; dielectric permittivity ; phase transition ; hysteresis loops ; magnetoelectric coupling Subject RIV BM - Solid Matter Physics ; Magnetism OECD category Condensed matter physics (including formerly solid state physics, supercond.) Institutional support FZU-D - RVO:68378271 UT WOS 000401196300012 EID SCOPUS 85019054149 DOI 10.1080/00150193.2017.1294039 Annotation Dielectric permittivity ϵ and polarization / electric field hysteresis loops of highly-resistive Li-doped non-relaxor Pb(Fe1/2Ta1/2)O3 ceramics obtained by one-step sintering of the mechanically activated mixture of starting oxides and Li2CO3 have been studied. Antiferromagnetic phase transition temperature TN ≈ 150 K was determined using Mossbauer spectroscopy studies at different temperatures. Though no anomalies in ϵ(T) curve at TN were observed, 1/ϵ(T) dependence exhibits change of the slope in the vicinity of TN. Anomalies in the temperature dependences of coercive field EC and derivative of the spontaneous polarization PS are observed near TN as well. These anomalies are attributed to magnetoelectric coupling. Workplace Institute of Physics Contact Kristina Potocká, potocka@fzu.cz, Tel.: 220 318 579 Year of Publishing 2018
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