Structure, dielectric and piezoelectric properties of (0.9−x)(Bi0.95La0.05)FeO3−xPbTiO3− 0.1BaZrO3 ceramics

Qiang Li, Yingjie Dong, Jinrong Cheng, Jianguo Chen
{"title":"Structure, dielectric and piezoelectric properties of (0.9−x)(Bi0.95La0.05)FeO3−xPbTiO3− 0.1BaZrO3 ceramics","authors":"Qiang Li, Yingjie Dong, Jinrong Cheng, Jianguo Chen","doi":"10.1109/SPAWDA.2015.7364524","DOIUrl":null,"url":null,"abstract":"(0.9-x)(Bi<sub>0.95</sub>La<sub>0.05</sub>)FeO<sub>3-x</sub>PbTiO<sub>3</sub>-0.1BaZrO<sub>3</sub> (BLF-xPT-BZ) ceramics were synthesized by the conventional solid state reaction method. The X-ray diffraction (XRD) results reflected that phase transformation from rhombohedral (R) to tetragonal (T) took place with increasing the PT content, and the coexistence R and T phases were observed at x = 0.35. The dielectric constant (ε<sub>r</sub>), dielectric loss (tanδ), remnant polarization (Pr) and piezoelectric coefficient (d<sub>33</sub>) increased initially and then decreased with increasing the PT content, and reach to maximum at x = 0.35. The TC, Td, ε<sub>r</sub>, d<sub>33</sub>, S and kp of 0.55BLF-0.35PT- 0.1BZ were 422 °C, 380 °C, 620, 162 pC/N, 0.3 % and 0.272, respectively. It was interesting that the maximum strain of BLF-xPT-BZ ceramics achieves about 0.3% under the electric field of 75 kV/cm, which was larger than that of BiScO<sub>3</sub>-PbTiO<sub>3</sub> ceramics.","PeriodicalId":205914,"journal":{"name":"2015 Symposium on Piezoelectricity, Acoustic Waves, and Device Applications (SPAWDA)","volume":"639 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2015 Symposium on Piezoelectricity, Acoustic Waves, and Device Applications (SPAWDA)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/SPAWDA.2015.7364524","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

(0.9-x)(Bi0.95La0.05)FeO3-xPbTiO3-0.1BaZrO3 (BLF-xPT-BZ) ceramics were synthesized by the conventional solid state reaction method. The X-ray diffraction (XRD) results reflected that phase transformation from rhombohedral (R) to tetragonal (T) took place with increasing the PT content, and the coexistence R and T phases were observed at x = 0.35. The dielectric constant (εr), dielectric loss (tanδ), remnant polarization (Pr) and piezoelectric coefficient (d33) increased initially and then decreased with increasing the PT content, and reach to maximum at x = 0.35. The TC, Td, εr, d33, S and kp of 0.55BLF-0.35PT- 0.1BZ were 422 °C, 380 °C, 620, 162 pC/N, 0.3 % and 0.272, respectively. It was interesting that the maximum strain of BLF-xPT-BZ ceramics achieves about 0.3% under the electric field of 75 kV/cm, which was larger than that of BiScO3-PbTiO3 ceramics.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
(0.9−x)(Bi0.95La0.05)FeO3−xPbTiO3−0.1BaZrO3陶瓷的结构、介电和压电性能
采用常规固相反应法制备了(0.9-x)(Bi0.95La0.05)FeO3-xPbTiO3-0.1BaZrO3 (BLF-xPT-BZ)陶瓷。x射线衍射(XRD)结果表明,随着PT含量的增加,材料发生了由菱形(R)向四方(T)相转变,在x = 0.35处出现了R相和T相共存的现象。介电常数(εr)、介电损耗(tanδ)、剩余极化(Pr)和压电系数(d33)随PT含量的增加先增大后减小,在x = 0.35时达到最大值。0.55BLF-0.35PT- 0.1BZ的TC、Td、εr、d33、S和kp分别为422°C、380°C、620、162 pC/N、0.3%和0.272。有趣的是,在75 kV/cm的电场下,BLF-xPT-BZ陶瓷的最大应变达到0.3%左右,比BiScO3-PbTiO3陶瓷的最大应变要大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Potential of Al2O3/GaN/Sapphire layered structure for high temperature SAW sensors Application of SAW gas chromatography in the early screening of lung cancer Research on the loss-less compression algorithm of the ultrasonic testing of rail First-principles study on the electronic structure and optical properties of Mn-doped NaNbO3 Development of cryptophane A-coated SAW methane gas sensor
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1