期刊文献+

电泳沉积PNN-PZT陶瓷厚膜及其电学性能研究 被引量:2

Electrophoretic Deposition and the Electrical Properties of the PNN-PZT Thick Films
下载PDF
导出
摘要 利用电泳沉积法分别在Al2O3/Pt和Pt金属基底上制备了厚度为10~40μm的0.3Pb(Ni1/3Nb2/3)O3-0.7Pb(Zr,Ti)O3(PNN-PZT)厚膜,研究了pH值、Zeta电位与PNN-PZT悬浮液稳定性的关系,探索了沉积电压、沉积时间与电泳沉积量的关系.结果表明,当添加少量分散剂聚乙二醇时,pH值在3.5~5.5较宽的范围内,悬浮液具有较高的Zeta电位,容易制得稳定的悬浮液.沉积电压为21V,沉积时间为5min时,在Pt金属基底上电泳沉积得到的PNN-PZT厚膜,经过1200℃烧结30min后,SEM显微结构分析表明,厚膜致密,晶粒得到充分生长.电学性能测试显示此厚膜具有良好的铁电介电性能,其剩余极化强度P可达20.8μC/cm2,介电损耗tanδ为3.2%. 0.3Pb(Ni1/3Nb2/3)O3-0.7Pb(Zr,Ti)O3(PNN-PZT) thick films(10-40μm) were prepared by electrophoretic deposition method on Al2O3/Pt plates and Pt metallic foils.The effect of pH value on the stability of PNN-PZT suspensions was studied by measuring the zeta potential.The relationship among the deposition voltage,time and the quality of PNN-PZT films were investigated.When the pH value is in the range of 3.5-5.5,the suspension with the 2wt% PEG is stable.When the deposited voltage and time are 21V and 5min,respectively,the PNN-PZT thick films deposited on the Pt foil are uniform and free of crack.After sintering at 1200℃ for 30min,the PNN-PZT films with high density are obtained.The PNN-PZT thick films show the high ferroelectric and dielectric properties with the remnant polarization of 20.8μC/cm2 and the loss tangent of about 3.2% at 1 kHz.And the frequency dependences of the dielectric spectra of the PNN-PZT thick films show the relaxor property.The piezoelectric constant calculated from the S-V curve tested using the SPM is 67pm/V.
出处 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2009年第6期1183-1188,共6页 Journal of Inorganic Materials
基金 国家自然科学基金(50675218) 国家重点基础研究发展计划(973)项目(2009CB623305)
关键词 PNN—PZT厚膜 电泳沉积 介电性能 电滞回线 PNN-PZT thick film electrophoretic deposition dielectric property polarization hysteresis loop
  • 相关文献

参考文献18

  • 1Harsanyi E. Method of Coating Radiant Bodies, U. S. Patent, No. 1897902, 1933.
  • 2Mayr H, Ordung M, Ziegler G. J. Mater. Sci. , 2006, 41 (24) : 8138-8143.
  • 3WangZ, Shemilt J, Xiao P. J. Eur. Ceram. Soc., 2002,22(2): 183-191.
  • 4Limmer S J, Seraji S, Wu Y, et al. Adv. Func. Mater. , 2002, 12 (1) : 59-64.
  • 5Tassel V J, Randall C A. J. Eur. Ceram. Soc. , 1999, 19(6/7) : 955-958.
  • 6Sarkar P, Nicholson S. J. Am. Ceram. Soc, , 1996, 79(8) : 1987- 2002.
  • 7Zhao J L, Wang X H, Li L T. Mater. Chem. Phys. , 2006, 99(2/ 3) : 350-353.
  • 8Li T, MaJ, Chen Y H. Ceram. Inter. , 2004,30(7) : 1803-1805.
  • 9Chen Y H, Ma J, Li T. Ceram. Inter. , 2004, 30(5) : 683-687.
  • 10Chen J, Fan H, Chen X, et al. J. Alloys Compd. , 2009, 478(1/ 2) : 853-857.

同被引文献10

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部