Structure, dielectric and ferroelectric properties of 0.92Na0.5Bi0.5TiO3-0.06BaTiO3-0.02K0.5Na0.5NbO3 lead-free ceramics: Effect of Co2O3 additive

被引:41
作者
Ma, H. Y. [1 ]
Chen, X. M. [1 ]
Wang, J. [1 ]
Huo, K. T. [1 ]
Lian, H. L. [2 ]
Liu, P. [1 ]
机构
[1] Shaanxi Normal Univ, Coll Phys & Informat Technol, Xian 710062, Peoples R China
[2] Xian Univ Posts & Telecommun, Sch Sci, Xian 710121, Peoples R China
基金
中国国家自然科学基金;
关键词
Electron microscopy; X-ray methods; Dielectric properties; Ferroelectric properties; FREE PIEZOELECTRIC CERAMICS; PHASE-TRANSITIONS; BARIUM-TITANATE; ELECTRICAL-PROPERTIES; RAMAN-SPECTROSCOPY; X-RAY; MICROSTRUCTURE; TEMPERATURE; ATMOSPHERES; DEPENDENCE;
D O I
10.1016/j.ceramint.2012.10.208
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
0.92Na(0.5)Bi(0.5)TiO(3)-0.06BaTiO(3)-0.02K(0.5)Na(0.5)NbO(3)+x wt% Co2O3 (NBKT-xCo, x=0, 0.2, 0.4, 0.6, 0.8) lead-free ferroelectric ceramics were prepared via a conventional solid state reaction method. Effects of Co2O3 additive on crystallite structure, microstructure, dielectric and ferroelectric properties of the NBKT-xCo ceramics were studied. X-ray diffraction results showed that the rhombohedral tetragonal morphotropic phase boundary existed in all the ceramics, with relative amount of tetragonal phase varying with the content of Co2O3. Average grain size, maximum value of dielectric constant, Curie temperature and ferroelectric properties of the ceramics were close related to the content of Co2O3. The dielectric anomaly caused by the phase transition between the ferroelectric phase and the so-called "intermediate phase" was observed in the ceramics with x <= 0.2, while it disappeared with further increasing x. All the ceramics showed a diffuse phase transition between the "intermediate phase" and the paraelectric phase. The change in the ferroelectric properties with changing the content of Co2O3 was discussed by considering the competitive effects among grain size, relative amount of the tetragonal phase and oxygen vacancies. (C) 2012 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:3721 / 3729
页数:9
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