Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/55993
Title: Preparation and characterization of Bi4–xPrxTi3O12 solid solutions
Authors: Klyndyuk, A. I.
Chizhova, E. A.
Poznyak, A. I.
Issue Date: 2017
Publisher: Уральский федеральный университет
Citation: 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.
Abstract: 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.
Keywords: LAYERED BISMUTH TITANATES
DIELECTRIC CONSTANT
DIELECTRIC LOSSES
ELECTRICAL CONDUCTIVITY
THERMO-EMF
THERMAL EXPANSION
URI: http://hdl.handle.net/10995/55993
RSCI ID: https://elibrary.ru/item.asp?id=32314604
ISSN: 2409-5613 (Print)
2411-1414 (Online)
DOI: 10.15826/chimtech/2017.4.4.01
metadata.dc.description.sponsorship: 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).
Origin: Chimica Techno Acta. 2017. Vol. 4. № 4
Appears in Collections:Chimica Techno Acta

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