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Ferroelectric soft mode and microwave dielectric relaxation in BaTiO.sub.3./sub.-PbMg.sub.1/3./sub.Nb.sub.2/3./sub.O.sub.3./sub. ceramics
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SYSNO ASEP 0543053 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Ferroelectric soft mode and microwave dielectric relaxation in BaTiO3-PbMg1/3Nb2/3O3 ceramics Author(s) Bovtun, Viktor (FZU-D) RID, ORCID, SAI
Nuzhnyy, Dmitry (FZU-D) RID, ORCID
Kempa, Martin (FZU-D) RID, ORCID
Ostapchuk, Tetyana (FZU-D) RID, ORCID
Skoromets, Volodymyr (FZU-D) RID
Suchanicz, J. (PL)
Czaja, P. (PL)
Petzelt, Jan (FZU-D) RID, ORCID, SAI
Kamba, Stanislav (FZU-D) RID, ORCID, SAINumber of authors 9 Article number 014404 Source Title Physical Review Materials. - : American Physical Society - ISSN 2475-9953
Roč. 5, č. 1 (2021)Number of pages 13 s. Language eng - English Country US - United States Keywords ferroelectrics ; phase transitions ; soft mode ; microwave relaxation Subject RIV BM - Solid Matter Physics ; Magnetism OECD category Condensed matter physics (including formerly solid state physics, supercond.) R&D Projects EF16_019/0000760 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GF20-20326L GA ČR - Czech Science Foundation (CSF) Method of publishing Limited access Institutional support FZU-D - RVO:68378271 UT WOS 000607538600003 EID SCOPUS 85100183676 DOI 10.1103/PhysRevMaterials.5.014404 Annotation BT-100x%PMN, x=0.075, 0.10, 0.15 were studied by the infrared reflectivity, time-domain terahertz transmission and microwave spectroscopies.The spectra show presence of a split soft phonon at all temperatures, similar to that observed in BT and PMN. Microwave dielectric dispersion was observed both below and above temperature of the diffuse permittivity maximum. The relaxations show no PMN-like freezing. So the ceramics cannot be considered as relaxor ferroelectrics, but rather as ferroelectrics with the diffuse phase transition. Workplace Institute of Physics Contact Kristina Potocká, potocka@fzu.cz, Tel.: 220 318 579 Year of Publishing 2022 Electronic address https://doi.org/10.1103/PhysRevMaterials.5.014404
Number of the records: 1