首页> 外文会议>International Symposium on Solid-State Ionic Devices III and 202nd Electrochemical Society Meeting Oct 20-24, 2002 Salt Lake City >STRUCTURE STABILIZATION AND IONIC CONDUCTION OF LI-DOPED CATION-DEFICIENT PEROVSKITE SOLID ELECTROLYTES
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STRUCTURE STABILIZATION AND IONIC CONDUCTION OF LI-DOPED CATION-DEFICIENT PEROVSKITE SOLID ELECTROLYTES

机译:掺锂的缺阳离子钙钛矿固体电解质的结构稳定和离子传导

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Undoped and Li-doped lanthanum titanates were prepared using oxides as the starting materials. Sintered samples were examined by XRD, SEM, EDX and AC impedance spectroscopy. It was observed that the powder mixture of La_2O_3 and TiO_2 could not form a La_(2/3)TiO_3 perovskite when heated at 1350℃ in air. A well-defined perovskite structure was obtained when the same powder mixture was heated in a reducing environment or added with more than 10 mol% of Li. The structure variation of Li-doped lanthanum titanate was rationalized on the basis of defect chemistry. The excess cation vacancies are believed to be the main reason for the instability of La_(2/3)TiO_3. The elimination of cation vacancies and structure stabilization were achieved by either the heat treatment under reducing atmosphere or the addition of Li ions. For conductivity measurements, a maximum conductivity of 2.51 x 10~(-5) S/cm was obtained when Li ions added reached 30 mol%. This result is consistent with the consideration based on the available vacancies and the charge carriers.
机译:使用氧化物作为起始原料制备未掺杂和锂掺杂的钛酸镧。通过XRD,SEM,EDX和AC阻抗谱检查烧结样品。观察到La_2O_3和TiO_2的粉末混合物在空气中于1350℃加热时不能形成La_(2/3)TiO_3钙钛矿。当将相同的粉末混合物在还原环境中加热或添加超过10 mol%的Li时,可获得明确的钙钛矿结构。在缺陷化学的基础上合理化了掺锂钛酸镧的结构变化。过量的阳离子空位被认为是La_(2/3)TiO_3不稳定性的主要原因。阳离子空位的消除和结构的稳定化是通过在还原气氛下进行热处理或添加锂离子来实现的。对于电导率测量,当添加的锂离子达到30 mol%时,最大电导率为2.51 x 10〜(-5)S / cm。该结果与基于可用空位和电荷载体的考虑一致。

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