Giant room-temperature electrostrictive coefficients in lead-free relaxor ferroelectric ceramics by compositional tuning
Author(s) -
Aman Ullah,
Hafiza Bushra Gul,
Amir Ullah,
Muhammad Sheeraz,
JongSeong Bae,
Wook Jo,
Chang Won Ahn,
Ill Won Kim,
Tae Heon Kim
Publication year - 2018
Publication title -
apl materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.571
H-Index - 60
ISSN - 2166-532X
DOI - 10.1063/1.5006732
Subject(s) - electrostriction , materials science , phase boundary , ferroelectricity , phase transition , condensed matter physics , dielectric , ceramic , tetragonal crystal system , temperature coefficient , electric field , ergodic theory , hysteresis , phase (matter) , thermodynamics , composite material , piezoelectricity , optoelectronics , chemistry , organic chemistry , quantum mechanics , physics , mathematical analysis , mathematics
A thermotropic phase boundary between non-ergodic and ergodic relaxor phases is tuned in lead-free Bi1/2Na1/2TiO3-based ceramics through a structural transition driven by compositional modification (usually named as “morphotropic approach”). The substitution of Bi(Ni1/2Ti1/2)O3 for Bi1/2(Na0.78K0.22)1/2TiO3 induces a transition from tetragonal to “metrically” cubic phase and thereby, the ergodic relaxor ferroelectric phase becomes predominant at room temperature. A shift of the transition temperature (denoted as TF-R) in the non-ergodic-to-ergodic phase transition is corroborated via temperature-dependent dielectric permittivity and loss measurements. By monitoring the chemical composition dependence of polarization-electric field and strain-electric field hysteresis loops, it is possible to track the critical concentration of Bi(Ni1/2Ti1/2)O3 where the (1 − x)Bi0.5(Na0.78K0.22)0.5TiO3-xBi(Ni0.5Ti0.5)O3 ceramic undergoes the phase transition around room temperature. At the Bi(Ni0.5Ti0.5)O3 content of x = ...
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