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材料导报  2023, Vol. 37 Issue (7): 21100234-6    https://doi.org/10.11896/cldb.21100234
  无机非金属及其复合材料 |
BNT基铁电陶瓷的温度诱导高电致应变响应及其机理研究
楚丙凯1, 刘璐璐1, 郝继功1,*, 李伟1,*, 曾华荣2
1 聊城大学材料科学与工程学院,山东 聊城 252059
2 中国科学院上海硅酸盐研究所,上海 200050
Study on the Temperature-induced High Strain Response and Mechanism of BNT-based Ferroelectric Ceramics
CHU Bingkai1, LIU Lulu1, HAO Jigong1,*, LI Wei1,*, ZENG Huarong2
1 School of Materials Science and Engineering,Liaocheng University, Liaocheng 252059, Shandong, China
2 Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
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摘要 近年来,钛酸铋钠(Bi0.5Na0.5)TiO3 (BNT)基铁电材料因具有高电致应变响应而受到广泛关注,并在驱动器方面展现出巨大的应用潜力。本工作采用传统固相法工艺制备了(1-x)(Bi0.5Na0.5)TiO3-x(Ba0.90Ca0.10)(Ti0.92Sn0.08)O3 (BNT-xBCTS, x=0.04~0.07)铁电陶瓷,研究了BCTS含量对BNT陶瓷的相结构、介电性能及电致应变性能的影响。通过分析高温下材料铁电/应变性能的变化和高温原位XRD/拉曼测试结果,明确了温度诱导BNT基陶瓷高电致应变产生的机理。结果表明,BNT-xBCTS (x=0.04~0.07)陶瓷均具有三方-四方两相共存结构,且三方相/四方相的含量比随着BCTS含量的增大逐渐减小。BCTS的引入促使BNT材料的铁电-弛豫相变温度(TF-R)向低温方向移动,并提高了BNT陶瓷材料室温下的电致应变性能。此外,BNT-xBCTS体系具有温度诱导高电致应变特征,在其TF-R附近,电致应变性能获得极大提升:BNT-0.05BCTS陶瓷在其TF-R(150 ℃)附近的单向应变值Suni达到0.463% (70 kV/cm电场下,测试频率1 Hz),对应的大信号压电常数d33*为661 pm/V。通过开展样品在室温和150 ℃下第一圈电滞回线/双向应变曲线测试,给出了材料在不同温度下电场诱导结构转变的具体演变过程,并证实了BNT基材料在其TF-R温度附近的高电致应变来源于电场诱导的遍历性弛豫态到铁电态的可逆转变。
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楚丙凯
刘璐璐
郝继功
李伟
曾华荣
关键词:  钙钛矿  钛酸铋钠  铁电  电致应变  相变    
Abstract: In recent years, bismuth sodium titanate (Bi0.5Na0.5)TiO3 (BNT)-based ferroelectric materials have received extensive attention due to their high electrostrain response, and it has shown great potential in the actuator application. In this work, (1-x)(Bi0.5Na0.5)TiO3-x(Ba0.90Ca0.10)(Ti0.92Sn0.08)O3 (BNT-xBCTS, x=0.04—0.07) ferroelectric ceramics were prepared by traditional solid-phase sintering process, and the influence of BCTS content on the phase structure, dielectric properties and electrostrain performance of BNT-based ceramics was studied. The mechanism of temperature-induced high strain was further analyzed combining with the high-temperature ferroelectric/strain properties and the high-temperature in-situ XRD and Raman results. Results showed that all compositions have coexisting rhombohedral and tetragonal phases, and the rhombohedral/tetragonal phase ratio decreases as the content of BCTS increases. The introduction of BCTS induces the ferroelectric-relaxor phase transition temperature TF-R of BNT moving to the low temperature, thereby increasing the electrostrain of the BNT material. Moreover, BNT-xBCTS materials exhibit temperature-induced high electrical strain behavior. Near its ferroelectric-relaxor phase transition temperature TF-R, the electrostrain response is greatly improved:BNT-0.05BCTS exhibits a large strain response near its TF-R (150 ℃):the unipolar strain Suni reaches 0.463% at 70 kV/cm, which corresponds to a large-signal piezoelectric constant d33* of 661 pm/V. By carrying out the mea-surement of first cycle P-E hysteresis loop and bipolar strain curve for samples, the structure evolution process induced by the electric field at different temperatures is disclosed, and it is confirmed that large strain near TF-R temperature originates from the inreversible transition from the ergodic relaxor phase to ferroelectric phase induced by the electric field.
Key words:  perovskite    bismuth sodium titanate    ferroelectric    electrostrain    phase transition
出版日期:  2023-04-10      发布日期:  2023-04-07
ZTFLH:  TM282  
基金资助: 山东省高等学校优秀青年创新团队支持计划(2019KJA025);山东省自然科学基金(ZR2020ME033;ZR2020ME031);中国科学院无机功能材料与器件重点实验室开放课题(KLIFMD202008)
通讯作者:  * 郝继功,聊城大学材料科学与工程学院副教授。2013年毕业于同济大学功能材料研究所,获材料科学与工程专业博士学位。主要从事无铅压电材料、电介质储能材料的研究,在国内外重要期刊发表论文50余篇。haojigong@lcu.edu.cn
李伟,聊城大学材料科学与工程学院教授。2014年毕业于同济大学功能材料研究所,获材料科学与工程专业博士学位;2018—2019年于澳大利亚卧龙岗大学访学。主要从事铁电/压电材料的组分设计和性能优化,在国内外知名期刊发表论文多篇。liwei_727@163.com   
作者简介:  楚丙凯,2019年6月毕业于聊城大学,获工学学士学位,2022年毕业于聊城大学材料科学与工程学院,获工学硕士学位。主要研究方向为钛酸铋钠基储能介质陶瓷的制备与性能。
引用本文:    
楚丙凯, 刘璐璐, 郝继功, 李伟, 曾华荣. BNT基铁电陶瓷的温度诱导高电致应变响应及其机理研究[J]. 材料导报, 2023, 37(7): 21100234-6.
CHU Bingkai, LIU Lulu, HAO Jigong, LI Wei, ZENG Huarong. Study on the Temperature-induced High Strain Response and Mechanism of BNT-based Ferroelectric Ceramics. Materials Reports, 2023, 37(7): 21100234-6.
链接本文:  
http://www.mater-rep.com/CN/10.11896/cldb.21100234  或          http://www.mater-rep.com/CN/Y2023/V37/I7/21100234
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