Bulk solid state rechargeable lithium ion battery fabrication with Al-doped Li7La3Zr2O12 electrolyte and Cu0.1V2O5 cathode

被引:61
作者
Jin, Ying [1 ]
McGinn, Paul J. [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
关键词
Solid-state battery; Solid electrolyte; Li7La3Zr2O12; Garnet structure; PERFORMANCE; CONDUCTION; XEROGEL; FILMS; ANODE;
D O I
10.1016/j.electacta.2012.11.059
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A simple, low-temperature route was developed to process bulk solid-state Li-ion batteries employing Al-doped Li7La3Zr2O12 solid electrolyte (thickness: similar to 0.5 mm; 25 degrees C conductivity; similar to 2 x 10(-4) S cm(-1)). A composite Cu0.1V2O5-based slurry was directly painted on Li7La3Zr2O12 and dried at 120 degrees C to prepare the cathode film. The opposite side of the electrolyte was subsequently exposed to molten Li to form the anode. The discharge capacity of the solid state battery was 53 mAh g(-1) (calculated based on the weight of active cathode material) at room temperature with 5 mu A cm(-2) discharging current. Severe capacity decay occurred after the initial discharging. A comparable liquid electrolyte battery was tested at room temperature for comparison and had a much slower decay rate. However, when the operating temperature of the solid state battery was increased to 50 degrees C, the cell performance significantly improved. At 50 degrees C, the battery exhibited 176 mAh g(-1) initial discharging capacity at 5 mu A cm(-2) current density and 93 mAh g(-1) initial capacity under a 10 mu A cm(-2) discharging current density. After 20 cycles, the capacity decayed to 68.6 mAh g(-1) when cycled at a 10 mu A cm(-2) current density. Impedance spectroscopy was used to investigate the interface resistance of the battery at different temperatures. The results indicated that both the cathode and anode interface resistance were dramatically reduced at 50 degrees C. The decrease in interface resistances at elevated temperature is proposed as the main reason for the observed battery performance enhancement. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:407 / 412
页数:6
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