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Название: Preparation and characterization of Bi4–xPrxTi3O12 solid solutions
Авторы: Klyndyuk, A. I.
Chizhova, E. A.
Poznyak, A. I.
Дата публикации: 2017
Издатель: Уральский федеральный университет
Библиографическое описание: Klyndyuk A. I. Preparation and characterization of Bi4–xPrxTi3O12 solid solutions / A. I. Klyndyuk, E. A. Chizhova, A. I. Poznyak // Chimica Techno Acta. — 2017. — Vol. 4, No. 4. — P. 210-217.
Аннотация: The Bi4–xPrxTi3O12 (BPT) solid solutions (x = 0.05, 0.10, 0.15) with small praseodymium content were prepared by solid-state method. Thermal, electric, and dielectric properties of BPT were studied. It was revealed that BPT titanates crystalize in аn orthorhombic structure and exhibit p-type semiconductivity. Dielectric constant of BPT increased, Curie temperature (TC), electrical conductivity and dielectric losses decreased, but lattice parameters and thermo-EMF coefficient remained practically unchanged with the increase of praseodymium content in layered Bi4–xPrxTi3O12. It was determined that activation energy of direct current (DC) electrical conductivity and linear thermal expansion coefficient (LTEC) of BPT changes at ferroelectric (FE) → paraelectric (PE) phase transition. The activation energy and LTEC changed below and above TC from 1.08–1.56 eV to 0.45–0.86 eV and from (9.10–10.80)·10–6 K–1 to (13.12–14.61)·10–6 K–1, respectively. The AC electrical conductivity studies of BPT illustrated short-range order with ionic translations assisted by small-polaron hopping.
Ключевые слова: LAYERED BISMUTH TITANATES
DIELECTRIC CONSTANT
DIELECTRIC LOSSES
ELECTRICAL CONDUCTIVITY
THERMO-EMF
THERMAL EXPANSION
URI: http://hdl.handle.net/10995/55993
Идентификатор РИНЦ: https://elibrary.ru/item.asp?id=32314604
DOI: 10.15826/chimtech/2017.4.4.01
Сведения о поддержке: This work was carried out within the framework of State Program of Scientific Investigations of Belarus Republic «Physical materials science, new materials and technologies » (subprogram «Materials science and technologies of materials», task 1.17).
Источники: Chimica Techno Acta. 2017. Vol. 4. № 4
Располагается в коллекциях:Chimica Techno Acta

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