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首页> 外文期刊>Journal of Materials Science >Studies on the ionic transport and structural investigations of La0.5Li0.5TiO3 perovskite synthesized by wet chemical methods and the effect of Ce, Zr substitution at Ti site
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Studies on the ionic transport and structural investigations of La0.5Li0.5TiO3 perovskite synthesized by wet chemical methods and the effect of Ce, Zr substitution at Ti site

机译:湿化学法合成钙钛矿型La0.5 Li0.5 TiO3 的离子迁移和结构研究及Ce,Zr置换在Ti位点的影响

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摘要

La0.5Li0.5TiO3 perovskite was synthesized by various wet chemical methods. By adopting low temperature methods of preparation lithium loss from the material is prevented. La0.5Li0.5TiO3 (LLTO) was formed with cubic symmetry at 1473 K. LLTO was formed at relatively lower temperature by using hydrothermal preparation method. PVA gel-decomposition route yield tetragonal LLTO on annealing the dried gel at 1473 K. By using gel-carbonate route LiTi2O4 minor phase was found to remain even after heat-treatment at 1473 K. The hydroxylation of LLTO was done in deionized water as well as in dilute acetic acid medium. By hydroxylation process incorporation of hydroxyls and leaching out of Li+ was observed from the material. The Li+ concentration of these compositions was examined by AAS. The electrical conductivities of these compositions were measured by dc and ac impedance techniques at elevated temperatures. The activation energies of electrical conduction for these compositions were estimated from the experimental results. The measured activation energy of Li+ conduction is 0.34 eV. Unhydroxylated samples exhibit only Li+ conduction, whereas, the hydroxylated LLTO show proton conductivity at 298–550 K in addition to Li+ conductivity. The effect of Zr or Ce substitution in place of Ti were attempted. La0.5Li0.5ZrO3 Perovskite was not formed; instead pyrochlore phase (La2Zr2O7) along with monoclinic ZrO2 phases was observed above 1173 K; below 1173 K cubic ZrO2 is stable. (La0.5Li0.5)2CeO4 solid solution was formed in the case of Ce substitution at Ti sublattice on heat-treatment up to 1673 K.
机译:通过多种湿化学方法合成了La0.5 Li0.5 TiO3 钙钛矿。通过采用低温制备方法,可以防止锂从材料中损失。在1473 K下形成立方对称的La0.5 Li0.5 TiO3 (LLTO)。采用水热法在较低温度下形成LLTO。 PVA凝胶分解路线在将干燥的凝胶于1473 K退火时产生四边形LLTO。通过使用凝胶-碳酸盐路线,即使在1473 K热处理后,LiTi2 O4 仍保留有次要相。 LLTO的制备是在去离子水和稀乙酸介质中进行的。通过羟基化过程,观察到了从材料中引入的羟基并浸出了Li + 。这些组合物的Li +浓度通过原子吸收光谱法检测。这些组合物的电导率是在升高的温度下通过直流和交流阻抗技术测量的。从实验结果估计了这些组合物的导电活化能。测得的Li +传导的活化能为0.34 eV。未羟基化的样品仅表现出Li + 导电性,而羟基化的LLTO除Li + 导电性外,在298-550 K时还显示质子导电性。尝试了用Zr或Ce代替Ti的效果。没有形成La0.5 Li0.5 ZrO3 钙钛矿。在1173 K以上观测到烧绿石相(La2 Zr2 O7 )和单斜晶ZrO2 相。低于1173 K立方ZrO2 是稳定的。在最高至1673 K的热处理条件下,在Ti亚晶格上进行Ce置换时,形成了(La0.5 Li0.5 )2 CeO4 固溶体。

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  • 来源
    《Journal of Materials Science》 |2005年第18期|4737-4748|共12页
  • 作者单位

    Materials Chemistry Division Indira Gandhi Centre for Atomic Research;

    Materials Chemistry Division Indira Gandhi Centre for Atomic Research;

    Materials Research Centre Indian Institute of Science;

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  • 正文语种 eng
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