Synthesis and sintering of Li1.3Al0.3Ti1.7(PO4)3 (LATP) electrolyte for ceramics with improved Li+ conductivity

被引:89
|
作者
Waetzig, Katja [1 ]
Rost, Axel [1 ]
Heubner, Christian [2 ]
Coeler, Matthias [1 ]
Nikolowski, Kristian [1 ]
Wolter, Mareike [1 ]
Schilm, Jochen [1 ]
机构
[1] Fraunhofer Inst Ceram Technol & Syst, Winterbergstr 28, D-01277 Dresden, Germany
[2] Tech Univ Dresden, Inst Mat Sci, D-01062 Dresden, Germany
关键词
All-solid-state batteries; Solid electrolyte; Lithium aluminum titanium phosphate LATP; High ionic conductivity; Separator; Sol-gel synthesis; IONIC-CONDUCTIVITY; SOLID ELECTROLYTES; CONDUCTORS; DENSE;
D O I
10.1016/j.jallcom.2019.153237
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 key material for all-solid-state batteries is the solid electrolyte. In concepts with high energy density and capacity, this Li+ conductive component has two essential functions: Substituting the liquid electrolyte in the cathode and separating the cathode from the anode. Therefore, the research on Li+ conductive solids is one important step to realize high performing all-solid-state batteries. In this study, two different methods of preparing Li1.3Al0.3Ti1.7(PO4)(3) (LATP) powder are compared with regard to particle size, phase purity and sintering properties. As top-down method the melting and as bottom-up route the sol-gel synthesis are applied. Spark Plasma Sintering (SPS) is used to densify the powders at temperatures between 800 and 1000 degrees C. The densities, the microstructures and the Li+ conductivities are compared in relation to the preparation method. Using sol-gel synthesis, the phase purity of the LATP powder is higher compared to the top-down route. The milling of the synthesized powder increases the homogeneity of the resulting microstructure and enhances the ionic conductivity. Room temperature Li+ conductivity of 1 x 10(-3) S cm(-1) with a high density of 99.4% was achieved with the milled, sol-gel synthesized powder at a sintering temperature of 1000 degrees C. (C) 2019 The Authors. Published by Elsevier B.V.
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页数:7
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