Structure, dielectric, ferroelectric and diffuse phase transition properties of the Ce, Ca hybrid doped BaTiO3 ceramics

被引:7
|
作者
Liu, Shujuan [1 ]
Zhang, Lixue [1 ]
Wang, Jiping [1 ]
Zhao, Yingying [1 ]
Wang, Xuan [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Mech Behav Mat, Xian 710049, Shaanxi, Peoples R China
关键词
Relaxor ferroelectrics; Curie-Weiss law; Constricted loops; Decreased P-r; RELAXOR FERROELECTRICS; ELECTRICAL-PROPERTIES; BEHAVIOR; POLARIZATION; TEMPERATURE; CROSSOVER;
D O I
10.1016/j.ceramint.2017.05.203
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Lead-free relaxor/diffuse ferroelectrics have attracted continued interest due to their unusual properties about broad maximum in temperature dependence of the dielectric permittivity and thin, narrow hysteresis loops. In this work, the diffuse behavior is studied in the Ce, Ca hybrid doped BaTiO3 ceramics (denoted as BT-8Ce-xCa, x = 10, 15, 20, 25 mol%) prepared by a conventional solid-state reaction. Pure perovskite phase structure can be observed in all the samples. Dense ceramics are successfully prepared and the grain size changes little with the increase of Ca content. The dielectric measurements show diffuse phase transition behaviors for all the samples, which are identified by a fit of the phenomenological equation with the xi character parameter for all the samples is about 1.80, the diffuse parameter Delta increases from 80.5 to 97.1, showing stronger diffuse behavior with more Ca content. As the Ca content increases, the Curie temperature (T-c) decreases. The decreased T-c and diffuse phase transition are diicussed from the role of Ca, Ce dopants. In addition, the diffuse ferroelectric properties of these ceramics are verified through the hysteresis loops changing to constricted loops with decreased P-r at low temperature which leads to larger P-max-P-r and larger energy storage density. This phenomenon is analyzed based on a field induced transition from diffuse ferroelectrics to normal ferroelectrics.
引用
收藏
页码:S36 / S42
页数:7
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