Electrical conductivity and conduction mechanisms in (Na0.5Bi0.5TiO3)1-x(BiScO3)x (0.00 x 0.25) solid solutions

被引:24
作者
Yang, F. [1 ]
Wu, P. [1 ]
Sinclair, D. C. [1 ]
机构
[1] Univ Sheffield, Dept Mat Sci & Engn, Mappin St, Sheffield S1 3JD, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
A-SITE NONSTOICHIOMETRY; IONIC-CONDUCTIVITY; PHASE-TRANSITIONS; LEAD; NA0.5BI0.5TIO3-BISCO3; CERAMICS; ZIRCONIA; ENERGY;
D O I
10.1039/c8tc04679d
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The electrical properties of (Na0.5Bi0.5TiO3)(1-x)(BiScO3)(x) (NBT-BS, 0.00 x 0.25) solid solutions are established by ac impedance spectroscopy and electromotive force transport number measurements. The bulk conductivity decreases with increasing BS incorporation but the oxide-ion transport number remains high (>0.85) over a wide compositional range 0.00 x 0.15 and drops to approximate to 0.7 for x 0.20. NBT-BS solid solutions can only present either predominant oxide-ion conduction or mixed ionic-electronic conduction behaviour, indicating that oxide-ion conduction cannot be fully eliminated by incorporation of BS. This is in contrast from our previous study where incorporation of approximate to 7% BiAlO3 (BA) can fully suppress the oxide-ion conduction in NBT. The conductivity-composition relationships of NBT-BS solid solutions are attributed to a competing effect from lattice expansion, which enlarges the channel for oxygen ion migration, with trapping between B-site acceptor ions, , and oxygen vacancies, , which decreases oxygen ion migration. Comparisons between NBT-BS, NBT-BA and NBT-BiGaO3 (BG) solid solutions suggest that small acceptor ions on the B-site are more effective in trapping oxygen vacancies and consequently more effective to suppress the oxide-ion conduction and thus reduce dielectric loss at elevated temperatures.
引用
收藏
页码:11598 / 11607
页数:10
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