Dielectric properties and relaxor behavior of Ba0.67Sr0.33TiO3-CaBi4Ti4O15 ceramics

Jing Xu, Hangxing Liu, Bo He, H. Hao, M. Cao
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Abstract

(1-x)Ba0.67Sr0.33TiO3(BST)+xCaBi4Ti4O15(CBT) (x=0, 2%, 4%, 6% and 8%) lead-free relaxor ferroelectric ceramics with submicro grain size of about 200nm were prepared by solidstate reactions. Structure and dielectric properties of BST-CBT have been investigated. X-ray diffraction patterns show a relative low degree of solubility as a result of coupled substitutions of Bi3+ and Ca2+ both on the A site and the specific structure of CBT. The temperature and frequency dependences of the dielectric constant indicate a crossover from a normal ferroelectric to relaxor behavior. The degrees of diffuseness and relaxor behavior are found to increase with the increasing amount of CBT. The frequency dependence of the temperature of dielectric peak Tm can be well described by Vogel-Fulcher relation. The activation energy Ea increases with x increasing, indicating the more and more energy for the polarization reversal of micropolar regions, which is associated with the enhanced interactions of polar domains.
Ba0.67Sr0.33TiO3-CaBi4Ti4O15陶瓷的介电性能和弛豫行为
采用固相反应法制备了(1-x)Ba0.67Sr0.33TiO3(BST)+xCaBi4Ti4O15(CBT) (x= 0,2%, 4%, 6%和8%)亚微晶粒尺寸约为200nm的无铅弛豫铁电陶瓷。研究了BST-CBT的结构和介电性能。x射线衍射图显示,由于Bi3+和Ca2+在a位和CBT的特定结构上的偶联取代,CBT的溶解度相对较低。介电常数的温度和频率依赖性表明从正常铁电到弛豫行为的交叉。随着CBT量的增加,弥漫性和松弛行为的程度增加。用Vogel-Fulcher关系可以很好地描述介电峰温度与频率的关系。活化能Ea随x的增大而增大,表明微极区极化反转的能量越来越大,这与极性域相互作用增强有关。
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