电解质
阳极
分离器(采油)
库仑法
金属锂
锂(药物)
材料科学
电化学
电极
电池(电)
金属
锂电池
快离子导体
化学工程
纳米技术
化学
冶金
有机化学
离子键合
热力学
医学
功率(物理)
物理化学
量子力学
离子
内分泌学
工程类
物理
作者
Burak Aktekin,Luise M. Riegger,Svenja‐K. Otto,Till Fuchs,Anja Henß,Jürgen Janek
标识
DOI:10.1038/s41467-023-42512-y
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 ∣ Li6PS5Cl ∣ 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.
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