电解质
堆栈(抽象数据类型)
材料科学
电流(流体)
电极
电流密度
接口(物质)
动力学(音乐)
机械
化学物理
热力学
复合材料
化学
声学
计算机科学
物理化学
量子力学
物理
毛细管数
毛细管作用
程序设计语言
作者
Michael J. Wang,Rishav Choudhury,Jeff Sakamoto
出处
期刊:Joule
[Elsevier]
日期:2019-07-12
卷期号:3 (9): 2165-2178
被引量:378
标识
DOI:10.1016/j.joule.2019.06.017
摘要
The replacement of conventional liquid electrolytes with solid electrolytes has the potential to safely enable energy-dense Li-metal anodes. Because of the challenges surrounding solid-solid interfaces, it is crucial to better understand the Li-metal-solid-electrolyte interface. This work utilizes stack pressure to correlate mechanics with the electrochemical behavior of Li-electrolyte cells during galvanostatic cycling. Symmetric cells are constructed using Li7La3Zr2O12 and tested using AC and DC techniques under dynamic stack pressure conditions. It is demonstrated that significant polarization occurs during galvanostatic cycling at a current-dependent “critical stack pressure.” Using reference electrodes, this effect is isolated to the Li stripping electrode. This suggests that at low pressures, the Li stripping rate exceeds the rate at which mechanical deformation replenishes the interface, inducing the formation of voids and ultimately increasing resistance. This analysis not only motivates the need for further understanding of the Li-metal-solid-electrolyte interface but also provides guidelines for the future design of all-solid-state batteries.
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