Oxygen-vacancy-related relaxation and conduction behavior in (Pb1-xBax)(Zr0.95Ti0.05)O3 ceramics

被引:106
作者
Zhang, Tian-Fu [1 ]
Tang, Xin-Gui [1 ]
Liu, Qiu-Xiang [1 ]
Lu, Sheng-Guo [2 ]
Jiang, Yan-Ping [1 ]
Huang, Xian-Xiong [1 ]
Zhou, Qi-Fa [3 ,4 ]
机构
[1] Guangdong Univ Technol, Guangzhou Higher Educ Mega Ctr, Sch Phys & Optoelect Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Univ Technol, Guangzhou Higher Educ Mega Ctr, Sch Mat & Energy, Guangzhou 510006, Guangdong, Peoples R China
[3] Univ So Calif, NIH Transducer Resource Ctr, Los Angeles, CA 90089 USA
[4] Univ So Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
基金
中国国家自然科学基金;
关键词
THIN-FILMS; DIELECTRIC-RELAXATION; ELECTRICAL-PROPERTIES; PIEZOELECTRIC PROPERTIES; PHASE-TRANSFORMATION; OPTICAL-PROPERTIES; POROSITY; FIELD; TRANSITION; PBZRO3;
D O I
10.1063/1.4900610
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
(Pb1-xBax)(Zr0.95Ti0.05)O-3 (x=0, 0.025, 0.05, 0.075 and 0.1) ceramics were prepared via a solid-state reaction route. Low-frequency (20 similar to 2x10(7) Hz) dielectric properties were investigated in the temperature region of 25-650 degrees C. Ba2+ doping can slightly reduce the phase transition temperature of ferroelectric to paraelectric. The dielectric diffuse anomaly in the dielectric relaxation was found in the high temperature region of 400-650 degrees C. Activation energy, calculated from the impedance and conductivity data of samples, suggests that the dielectric relaxation is due to oxygen vacancies generated during the sintering process. Ba2+ doping can reduce significantly the concentration of oxygen vacancies, and slightly enhance activation energy for the migration of oxygen vacancies. Results of activation energy calculated from impedance and conductance suggest that the dielectric relaxation is due to the short-range hopping of oxygen vacancies, and the conduction due to the movement of doubly-ionized oxygen vacancies. (C) 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License.
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页数:11
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