期刊文献+

Mo掺杂对高纯Ce1-xNdxO2-x/2(x=0.10,0.15)体系烧结温度及晶界电性能的影响

Effects of Mo-dopant on Sintering Temperature and Grain Boundary Conductivity of High-purity Ce_(1-x)Nd_xO_(2-x/2)(x=0.10,0.15) Systems
下载PDF
导出
摘要 用柠檬酸硝酸盐法制备高纯Ce1-xNdxO2-x/2(x=0.10,0.15)固溶体,加入摩尔分数为5%的Mo,研究了Mo掺杂对烧结温度、结构及电性能的影响.通过X射线衍射、电感偶合等离子体和场发射扫描电镜等手段对氧化物进行了结构表征,采用交流阻抗谱测试其电性能.柠檬酸硝酸盐法制备的前驱体经1450℃烧结24 h得到致密度大于96%的陶瓷材料;加入5%Mo,在1250℃下烧结8 h即可达到理想的致密度(>95%).加入Mo在烧结过程中可加快晶界迁移,促进晶粒生长,显著提高了晶界电导率.在600℃时Ce0.85Nd0.15O1.925的晶界电导率为2.56 S/m,加入Mo后材料的电导率增加到5.62 S/m. The pure Ce1-xNdxO2-x/2(x =0. 10, 0. 15) solid solutions were synthesized via citric-nitrate method and the effects of 5% (molar fraction) Mo-dopant on the sintering temperature and grain boundary conductivities of theCe1-xNdxO2-x/2(x =0. 10, 0. 15) were discussed. Their structures and ionic conductivities were characterized via X-ray Diffraction (XRD), Inductively Coupled Plasma (ICP), field-emission scanning electron microscopy(FE-SEM) and electrochemical impedance spectroscopy(EIS). The results show that the precurors synthesized via citric-nitrate method have a good sinterability with relative density of 〉 96% after being sintered at 1450℃ for 24 h. With Mo-dopant, the relative density of 〉95% was reached after being sintered at 1250℃ for 8 h and the grain boundary conductivity increased greatly because of the increase of grain size. The grain boundary conductivty at 600℃ for Ceo.ssNdo. 15Oi.925 increased from 2.56 S/m to 5.62 S/m with Mo-dopant.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2008年第9期1866-1869,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20331030,20671088) 吉林省科技发展计划(批准号:20070510)资助
关键词 固体电解质 电导率 晶界 掺杂 Solid state electrolyte Conductivity Grain boundary Doping
  • 相关文献

参考文献13

  • 1Zhang T. S. , Ma J. , Kong L. B. , et al.. Solid State Ionics[J] , 2004, 167:203-207
  • 2Fagg D. P. , Abrantes J. C. C. , Perez-coll D. , et al.. Electrochimica Acta[J], 2003, 48:1023-1029
  • 3Gil V. , Tartaj J. , Moure C. , et al.. Ceram. Int. [J] , 2007, 33:471-475
  • 4Zhang T. S. , Hing P. , Huang H. T.. J. Mater. Sci. [J] , 2002, 37:997-1003
  • 5Kleinlogel C. M., Gauckler L. J.. J. Electroceram. [J], 2000, 5(3) : 231-243
  • 6Yoshida H. , Miura K. , Fukui T. , et al.. J. Powder Sources[J], 2002, 106:136-141
  • 7Lewis G. S. , Atkinson A. , Steele B. C. H. , et al.. Solid State Ionics[J] , 2002, 152/153:567-573
  • 8Chen P. L. , Chen I. W.. J. Am. Ceram. Soc. [J], 1993, 76:1577-1583
  • 9Chen P. L. , Chen I. W.. J. Am. Ceram. Soc. [J], 1996, 79:1793-1800
  • 10周德凤,叶俊峰,李东风,姜新华,孟健.Sm,Pr掺杂CeO_2和CeMoO_(15)基固体电解质的结构与性能[J].高等学校化学学报,2007,28(11):2026-2029. 被引量:8

二级参考文献13

  • 1周德凤,薄其兵,王秋艳,王敬平,吕敏峰,刘建芬,曹学强,邢献然,孟健.新型固体电解质Ce_(6-x)Sm_xMoO_(15-δ)(0≤x≤1.2)的合成及电性质[J].高等学校化学学报,2005,26(10):1791-1794. 被引量:5
  • 2Gaetano C. , Lorenzo M. , Vincenzo M. , et al.. Solid State Ionics[J], 2005, 176:1505-1512
  • 3Peng R. R. , Xia C. R. , Peng D. K. , et al.. Mater. Lett. [J], 2004, 58:604-608
  • 4Wang F. Y. ,Chen S. Y. , Cheng S. F.. Electrochem. Commun. [J] , 2004, 6:743-746
  • 5Sha X. Q., Lv Z., Huang X. Q., et al.. J. Alloys Compounds[J], 2007, 428:59-64
  • 6Aitken E. A. , Bartram S. F. , Juenke E. F.. Inorg. Chem. [J] , 1964, 3:949-954
  • 7Bo Q. B., Feng J., Che P., et al.. J. Phys. : Condensed Matter[J], 2003, 15:5181-5189
  • 8Bo Q. B. , Sun G. X. , Meng J.. J. Physics and Chemistry of Solids[J] , 2006, 67:732-737
  • 9McBride J. R. , Hass K. C. , Poindexter B. D. , et al.. J. Appl. Phys. [J], 1994, 76:2435-2441
  • 10Haro-Poniatowski E. Jouanne M. , Morhange J. F. , et al.. Applied Surface Science[ J] , 1998, 127-129:674-678

共引文献7

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