z-logo
open-access-imgOpen Access
Crystal structure and dielectric properties of layered perovskite-like solid solutions Bi3−x Gdx TiTaO9 (x = 0.0, 0.1, 0.2, 0.3) with high Curie temperature
Author(s) -
S. V. Zubkov
Publication year - 2021
Publication title -
journal of advanced dielectrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.38
H-Index - 13
eISSN - 2010-135X
pISSN - 2010-1368
DOI - 10.1142/s2010135x2160016x
Subject(s) - aurivillius , curie temperature , orthorhombic crystal system , materials science , condensed matter physics , perovskite (structure) , crystallography , crystal structure , solid solution , dielectric , thermodynamics , physics , ferroelectricity , ferromagnetism , chemistry , optoelectronics , metallurgy
The Aurivillius phases [Bi 2 O 2 ][A[Formula: see text][Formula: see text]O[Formula: see text]] are well-known ferroelectrics with high Curie temperatures [Formula: see text]. High-temperature piezoceramics Bi[Formula: see text][Formula: see text]TiTaO 9 (BGdTTa, [Formula: see text]= 0.0, 0.1, 0.2, 0.3) were prepared by a solid-state reaction method. The structural and electrophysical characteristics of BGdTTa ceramics have been studied. According to the data of powder X-ray diffraction, all the compounds are single-phase with the structures of two-layer Aurivillius phases ([Formula: see text] = 2) with the orthorhombic crystal lattice (space group A2 1 am). The temperature dependence of the relative permittivity [Formula: see text]/[Formula: see text] ([Formula: see text] of the compounds was measured and showed that the Curie temperature [Formula: see text] of perovskite-like oxides Bi[Formula: see text][Formula: see text]TiTaO 9 increases linearly with an increase in the substitution parameter [Formula: see text] to [Formula: see text] = 925[Formula: see text]C. The activation energies of charge carriers have been found in different temperature ranges.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here