The effect of 24c-site (A) cation substitution on the tetragonal-cubic phase transition in Li7-xLa3-xAxZr2O12 garnet-based ceramic electrolyte

被引:136
作者
Rangasamy, Ezhiylmurugan [1 ]
Wolfenstine, Jeff [2 ]
Allen, Jan [1 ]
Sakamoto, Jeff [1 ]
机构
[1] Michigan State Univ, Dept Chem Engn & Mat Sci, E Lansing, MI 48824 USA
[2] USA, Res Lab, RDRL SED C, Adelphi, MD 20783 USA
关键词
Solid-electrolyte; Garnet; Ce; Cubic; Li vacancies; Hot-pressing; YTTRIUM-IRON-GARNET; SOLID-ELECTROLYTE; IONIC-CONDUCTIVITY; LITHIUM; LI7LA3ZR2O12; STATE; AL; TRANSPORT; GA;
D O I
10.1016/j.jpowsour.2012.12.076
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The garnet-type ceramic electrolyte of nominal composition Li7La3Zr2O12 can exist in the tetragonal and cubic form. This article investigates the tetragonal to cubic phase transition based on super-valent cation substitution on the 24c site typically occupied by La (3+) in the garnet structure. Ce (4+) was selected as the super-valent cation represented as x in Li7-xLa3-xCexZr2O12. The doping study showed that cubic LLZO was stabilized for Ce >= 0.2. These data agree with most literature reports suggesting that the creation of Li vacancies, while maintaining oxygen stoichiometry, is necessary to stabilize cubic LLZO. Moreover, this work suggests a critical Li vacancy concentration (0.12-0.4 mol per mole of Li7La3Zr2O12) is necessary to stabilize cubic LLZO. While the addition of Ce stabilized cubic LLZO, the total ionic conductivity (0.014 mS cm(-1)) was considerably lower compared to Al and Ta doped LLZO (0.4-0.9 mS cm(-1), respectively). The lower conductivity is likely due to CeO2 precipitation at grain boundaries. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:261 / 266
页数:6
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