期刊文献+

Ln_(0.6)Sr_(0.4)FeO_(3-δ)(Ln=La、Nd、Ce)阴极材料的制备与表征 被引量:5

Study on preparation and characterization of Ln_(0.6)Sr_(0.4)FeO_(3-δ)(Ln=La,Nd,Ce) for IT-SOFC cathodes
下载PDF
导出
摘要 以甘氨酸硝酸盐水溶液为前驱体合成了Sr掺杂的稀土铁酸盐Ln0.6Sr0.4FeO3-δ(Ln=La、Nd、Ce)粉体。对制备过程的化学键变化、样品的热稳定性、物相形成过程及导电性进行了表征。结果表明,甘氨酸硝酸盐合成法成相温度低于1000℃。坯体烧结较粉状样品更有利于钙钛矿物相的形成,La0.6Sr0.4FeO3-δ及Nd0.6Sr0.4FeO3-δ坯体1000℃煅烧2h即可形成近乎单一的钙钛矿相(ABO3);Ce0.6Sr0.4FeO3-δ是CeO2立方萤石相和产物钙钛矿相共存,两相难分主次。合成样品低温下的导电行为符合小极化子导电机制;1200℃烧结的La0.6Sr0.4FeO3-δ样品在测试全温度范围内(450~800℃)电导率超过100S/cm,Nd0.6Sr0.4FeO3-δ在中温区(600~800℃)电导率>60S/cm;Ce0.6Sr0.4FeO3-δ样品的电导率不理想。 Ln0.6Sr0.4FeO3-δ(Ln=La, Nd, Ce) composite oxides with Sr doped at A-site were prepared using glycine-nitrate aqueous solution as precursors. The structure and preparation process were analyzed by means of FT-IR and TG-DTA and X-ray diffractometer. The electrical conductivities of samples were determined by DC four-probe technique. The results showed that the temperature of forming structure is lower than 1000°C, the perovskite-type phase of products has obtained at the moment of ignition. The Ln0.6Sr0.4FeO3-δ wafer is almost a single perovskite-type phase after sintered at 1000°C for 2h, while the powder exhibits impure peaks after sintered at 1400°C for 4 h, which implies material state has an important effects on phase forming. Two phases with fluorite and perovskite phase presents in Ln0.6Sr0.4FeO3-δ. The electrical conductivity certified that the hopping of small polaron is the dominating mechanism at low temperature. Both of the Ln0.6Sr0.4FeO3-δ and Ln0.6Sr0.4FeO3-δ, the electrical conductivity was over 60 S/cm, and that of the Ln0.6Sr0.4FeO3-δ sample sintered at 1200°C for 2h was over 100 S/cm in the range of 450-800°C. The electrical property of Ln0.6Sr0.4FeO3-δ was disillusionary.
出处 《功能材料》 EI CAS CSCD 北大核心 2005年第6期865-868,共4页 Journal of Functional Materials
基金 安徽省教育厅自然科学基金资助项目(2004kj326)
关键词 掺杂稀土铁酸盐 中温固体氧化物燃料电池 甘氨酸-硝酸盐法 阴极材料 电导率 Differential thermal analysis Electric conductivity Electrochemistry Fourier transform infrared spectroscopy Sintering Solid oxide fuel cells Thermogravimetric analysis X ray diffraction analysis
  • 相关文献

参考文献15

  • 1Doshi R, Richards V L, Carter J D, et al. [J]. J Electrochem Soc, 1999,146(4): 1273-1278.
  • 2Teraoka Y, Nobunaga T, Okamoto K, et al. [J]. Solid State Ionics, 1991,48: 207.
  • 3Tu H Y,Takeda Y,Imanishi N,et al. [J]. Solid State Ionics, 1997,100 : 283-288.
  • 4Ishihara T,Fukui S, Nishiguchi H,et al. [J]. J Electrochem Soc,2002,149(7) : A823-A828.
  • 5Tai L W,Nasrallah M M,Anderson H U,et al. [J]. Electrochemical Society, 1993,93 (4): 241-251.
  • 6Kostogloudis G C,Tsiniarakis G,Ftikos C. [J]. Solid State Ionics, 2000 , 135: 529-535.
  • 7Simner S P,Bonnett J F,Canfield N L, et al. [J]. J Power Sources, 2003,113:1-10.
  • 8Xie G,Ma W H,Chen S R,et al. [J]. J Rare Earths,2003,21(1) :94-97.
  • 9徐庆,黄端平,陈文,王皓,袁润章.La_(0.6)Sr_(0.4)Co_(1-y)Fe_yO_3钙钛矿复合氧化物的GNP法合成与导电性能[J].高等学校化学学报,2003,24(12):2271-2274. 被引量:7
  • 10Chick L A,Pederson L R,Maupin G D,et al. [J]. Materials Letters, 1990,10(1,2): 6-12.

二级参考文献9

共引文献63

同被引文献35

引证文献5

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