Eu~(3+)掺杂钛酸锶钡陶瓷的介电性能实验研究
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  • 英文篇名:Experimental Study on Dielectric Properties of Eu~(3+) -doped Barium Strontium Titanate
  • 作者:李勰 ; 王会 ; 王婷婷 ; 朱晓东
  • 英文作者:LI Xie;WANG Hui;WANG Tingting;ZHU Xiaodong;Department of Material and Chemical Engineering, Ningbo University of Technology;Shanghai Advanced Research Institute;Ningbo Academy of Product Quality Supervision & Inspection;
  • 关键词:BST陶瓷 ; 钙钛矿 ; 稀土掺杂 ; 介电常数 ; 固溶体
  • 英文关键词:BST ceramics;;perovskite phase;;rare earth-doped;;dielectric constant;;solid solution
  • 中文刊名:TCXB
  • 英文刊名:Journal of Ceramics
  • 机构:宁波工程学院材料与化学工程学院;中国科学院上海高等研究院;宁波市产品质量监督检验研究院;
  • 出版日期:2019-02-15
  • 出版单位:陶瓷学报
  • 年:2019
  • 期:v.40
  • 基金:国家自然科学基金项目(21405085)
  • 语种:中文;
  • 页:TCXB201901016
  • 页数:6
  • CN:01
  • ISSN:36-1205/TS
  • 分类号:48-53
摘要
本文设计了氧化铕(Eu_2O_3)掺杂的(Ba_(0.7)Sr_(0.3))TiO_3(后简称BST)电子陶瓷。用XRD和SEM等分析测试手段研究了该陶瓷的相组成、微观结构;用阻抗分析仪测定分析了介电常数和介电损耗。结果表明:在BST陶瓷中掺入微量Eu_2O_3,可以使得BST陶瓷在室温下的介电常数降低,并且随着掺入量的增加下降加快。而介电损耗(tanδ)则先减小后增大,当Eu含量为0.03%时,tanδ最低。通过对该材料进行微观分析发现,Eu掺杂后BST陶瓷仍为钙钛矿结构,无其他杂相生成,但晶粒会发生变化,当掺杂量为0.05%时,晶粒发育最为完整;可见Eu掺杂确实能够改变BST陶瓷的微观结构及介电性能。
        In this paper special formulas were designed for Eu_2O_3-doped(Ba_(0.7)Sr_(0.3)) TiO_3 electronic ceramics. Then samples were prepared by solid-state reaction sintering method. XRD and SEM were used to analyze their phase composition and microstructure. The piezoelectric impedance analyzer was used to analyze their dielectric constant and dielectric loss. The results showed that when Eu_2O_3 was doped, the dielectric constant of the ceramics was reduced at room temperature. However, the dielectric loss(tanδ) decreased first and then increased.When the Eu content was 0.03%, the tanδ was the lowest. The microstructure analysis found that with Eu doping, the BST ceramics were still composed of the perovskite phase and tungsten bronze phase, but the grains of the samples changed. When the doping was 0.05%, their crystal development was the best. Therefore, Eu doping could obviously change the ceramic microstructure and dielectric properties.
引文
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