Colossal dielectric permittivity in hydrogen-reduced rutile TiO2 crystals

被引:62
|
作者
Li, Jinglei [1 ,2 ]
Li, Fei [1 ,2 ]
Zhu, Xuhui [1 ,2 ]
Lin, Dabin [3 ]
Li, Quanfu [4 ]
Liu, Weihua [4 ]
Xu, Zhuo [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Elect Mat Res Lab, Key Lab Minist Educ, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Int Ctr Dielect Res, Xian 710049, Peoples R China
[3] Xian Technol Univ, Lab Thin Film Tech & Opt Test, Xian 710032, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Microelect, Sch Elect & Informat Engn, Xian 710049, Peoples R China
基金
对外科技合作项目(国际科技项目); 中国国家自然科学基金;
关键词
Colossal dielectric permittivity; Hydrogen-reduced TiO2 single crystal; Electronic relaxation polarization; ELECTRICAL-PROPERTIES; THERMOELECTRIC-POWER; RAMAN-SPECTROSCOPY; CACU3TI4O12; CONDUCTIVITY; RESONANCE; NIOBIUM;
D O I
10.1016/j.jallcom.2016.09.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
(Nb + In) co-doped rutile TiO2 (TINO) ceramics have received considerable attention, due to their high dielectric permittivity (on the order of 10,000) and low loss factor (<0.05) over a broad temperature/frequency range. The high dielectric permittivity of TINO has been attributed to a special defect-dipole structure. Here, we observed a similar dielectric behavior in hydrogen-reduced rutile TiO2 crystals, where the colossal dielectric permittivity of similar to 30,000 and the low loss factor of similar to 0.05 exist in the temperature range of 30-480 K (frequency at 10 similar to 10(5) Hz). Based on the investigations on the phase microstructures, the elemental valences, impedance spectroscopy, nonlinear I-V behavior and dielectric response, the colossal dielectric permittivity of the hydrogen-reduced rutile TiO2 crystals was thought to be associated with the electronic relaxation polarization mechanism. This research further revealed that the weak-binding electron is the most critical factor for the high dielectric permittivity in rutile TiO2 system, while a special defect-dipole structure may not be a preliminary requirement. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:375 / 380
页数:6
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