Interface Instability of Fe-Stabilized Li7La3Zr2O12 versus Li Metal

被引:95
作者
Rettenwander, Daniel [1 ,2 ]
Wagner, Reinhard [3 ]
Reyer, Andreas [3 ]
Bonta, Maximilian [4 ]
Cheng, Lei [5 ]
Doeff, Marca M. [5 ]
Limbeck, Andreas [4 ]
Wilkening, Martin [1 ,2 ]
Amthauer, Georg [3 ]
机构
[1] Graz Univ Technol, Inst Chem & Technol Mat, Graz, Austria
[2] Graz Univ Technol, Inst Chem & Technol Mat, Christian Doppler Lab Lithium Batteries, Graz, Austria
[3] Univ Salzburg, Dept Chem & Phys Mat, Salzburg, Austria
[4] Vienna Univ Technol, Inst Chem Technol & Anal, Vienna, Austria
[5] Univ Calif Berkeley, Energy Storage & Distributed Resources Div, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
基金
奥地利科学基金会;
关键词
CRYSTAL-CHEMISTRY; ION CONDUCTION; SPECTROSCOPY;
D O I
10.1021/acs.jpcc.7b12387
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 interface stability versus Li represents a major challenge in the development of next-generation all-solid-state batteries (ASSB), which take advantage of the inherently safe ceramic electrolytes. Cubic Li7La3Zr2O12 garnets represent the most promising electrolytes for this technology. The high interfacial impedance versus Li is, however, still a bottleneck toward future devices. Herein, we studied the electrochemical performance of Fe3+-stabilized Li7La3Zr2O12 (LLZO:Fe) versus Li metal and found a very high total conductivity of 1.1 mS cm(-1) at room temperature but a very high area specific resistance of similar to 1 k Omega cm(2). After removing the Li metal electrode we observe a black surface coloration at the interface, which clearly indicates interfacial degradation. Raman- and nanosecond laser-induced breakdown spectroscopy reveals, thereafter, the formation of a 130 mu m thick tetragonal LLZO interlayer and a significant Li deficiency of about 1-2 formula units toward the interface. This shows that cubic LLZO:Fe is not stable versus Li metal by forming a thick tetragonal LLZO interlayer causing high interfacial impedance.
引用
收藏
页码:3780 / 3785
页数:6
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