SEI growth on Lithium metal anodes in solid-state batteries quantified with coulometric titration time analysis

被引:47
作者
Aktekin, Burak [1 ,2 ]
Riegger, Luise M. [1 ,2 ]
Otto, Svenja-K. [1 ,2 ]
Fuchs, Till [1 ,2 ]
Henss, Anja [1 ,2 ]
Janek, Juergen [1 ,2 ]
机构
[1] Justus Liebig Univ Giessen, Inst Phys Chem, D-35392 Giessen, Germany
[2] Justus Liebig Univ Giessen, Ctr Mat Res, D-35392 Giessen, Germany
关键词
ELECTROLYTE INTERPHASE; INTERFACE STABILITY; CAPACITY LOSS; TEMPERATURE; KINETICS;
D O I
10.1038/s41467-023-42512-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lithium-metal batteries with a solid electrolyte separator are promising for advanced battery applications, however, most electrolytes show parasitic side reactions at the low potential of lithium metal. Therefore, it is essential to understand how much (and how fast) charge is consumed in these parasitic reactions. In this study, a new electrochemical method is presented for the characterization of electrolyte side reactions occurring on active metal electrode surfaces. The viability of this new method is demonstrated in a so-called anode-free stainless steel divide Li6PS5Cl divide Li cell. The method also holds promise for investigating dendritic lithium growth (and dead lithium formation), as well as for analyzing various electrolytes and current collectors. The experimental setup allows easy electrode removal for post-mortem analysis, and the SEI's heterogeneous/layered microstructure is revealed through complementary analytical techniques. We expect this method to become a valuable tool in the future for solid-state lithium metal batteries and potentially other cell chemistries. In lithium-metal batteries, it is vital to quantify electrolyte side reactions occurring at the metal anode surface. Here, the authors introduce an electrochemical technique, using a series of small-step lithium deposition followed by open circuit voltage analysis, to accurately measure these reactions.
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页数:14
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