材料科学
陶瓷
去湿
电解质
蛋白质丝
纳米技术
电化学
显微镜
复合材料
化学物理
渗透(战争)
化学
薄膜
光学
电极
物理化学
工程类
物理
运筹学
作者
Eric Kazyak,Regina García-Méndez,William S. LePage,Asma Sharafi,Andrew L. Davis,Adrian J. Sanchez,Kuan‐Hung Chen,Catherine G. Haslam,Jeff Sakamoto,Neil P. Dasgupta
出处
期刊:Matter
[Elsevier BV]
日期:2020-03-04
卷期号:2 (4): 1025-1048
被引量:340
标识
DOI:10.1016/j.matt.2020.02.008
摘要
Solid-state electrolytes (SSEs) have attracted substantial attention for next-generation Li-metal batteries, but Li-filament propagation at high current densities remains a significant challenge. This study probes the coupled electrochemical-morphological-mechanical evolution of Li-metal-Li7La3Zr2O12 interfaces. Quantitative analysis of synchronized electrochemistry with operando video microscopy reveals new insights into the nature of Li propagation in SSEs. Several different filament morphologies are identified, demonstrating that a singular mechanism is insufficient to describe the complexity of Li propagation pathways. The dynamic evolution of the structures is characterized, which demonstrates the relationships between current density and propagation velocity, as well as reversibility of plated Li before short-circuit occurs. Under deep discharge, void formation and dewetting are directly observed, which are directly related to evolving overpotentials during stripping. Finally, similar Li penetration behavior is observed in glassy Li3PS4, demonstrating the relevance of the new insights to SSEs more generally.
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