Dielectric Properties of (Bi0.5K0.5)ZrO3 Modified (K0.5Na0.5)NbO3 Ceramics as High-Temperature Ceramic Capacitors

被引:12
|
作者
Yan, Tianxiang [1 ,2 ,3 ]
Ren, Shaokai [1 ]
Ma, Xing [1 ]
Han, Feifei [1 ]
Fang, Liang [1 ]
Peng, Biaolin [4 ,5 ]
Liu, Laijun [1 ]
Kuang, Xiaojun [1 ]
Elouadi, Brahim [2 ]
机构
[1] Guilin Univ Technol, Coll Mech & Control Engn, Coll Mat Sci & Engn, Guangxi Univ Key Lab Nonferrous Met Oxide Elect F, Guilin 541004, Peoples R China
[2] Univ La Rochelle, CNRS, UMR 7356, LaSIE, Ave Michel Crepeau, F-17042 La Rochelle 01, France
[3] Guilin Univ Technol, Guangxi Sci Expt Ctr Min Met & Environm, Guilin 541004, Peoples R China
[4] Guangxi Univ, Sch Phys Sci & Technol, Nanning 530004, Peoples R China
[5] Guangxi Univ, Guangxi Key Lab Relativist Astrophys, Nanning 530004, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Ceramics; dielectric properties; impedance spectroscopy; oxygen vacancies; ELECTRICAL-PROPERTIES; PHASE-DIAGRAM; THICK-FILMS; MICROSTRUCTURE; PERMITTIVITY;
D O I
10.1007/s11664-018-6641-7
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
(1 - x)K0.5Na0.5NbO3-x(Bi0.5K0.5)ZrO3 [abbreviated as (1 - x)KNN-xBKZ, 0 <= x <= 0.08] lead-free ceramics have been fabricated by a solid-state processing route. Based on the x-ray diffraction data and temperature-dependent dielectric characteristics, an orthorhombic phase for x <= 0.03 and single rhombohedral one for x >= 0.05 at room temperature were determined. The cell volume firstly increases, then decreases and finally increases with increasing BKZ, depending on ionic size and crystallographic structure. For the sample of x = 0.05, a temperature-stable high permittivity (similar to 1736 +/- 15%) along with low dielectric loss tangent (<= 5%) is recorded from 158 degrees C to 407 degrees C. In addition, the activation energies of dielectric relaxation and dc conductivity at high temperatures were characterized by impedance spectroscopy. A combined effect of lattice distortion and oxygen vacancies on the magnitude of activation energies was discussed.
引用
收藏
页码:7106 / 7113
页数:8
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