阳极
电解质
材料科学
电镀(地质)
金属锂
锂(药物)
化学工程
冶金
化学
电极
医学
内科学
物理
工程类
地球物理学
物理化学
作者
Dominic L. R. Melvin,Marco Siniscalchi,Dominic Spencer Jolly,Bingkun Hu,Ziyang Ning,Shengming Zhang,Junfu Bu,Shashidhara Marathe,Anne Bonnin,Johannes Ihli,Gregory J. Rees,Patrick S. Grant,Charles W. Monroe,T.J. Marrow,Guanchen Li,Peter G. Bruce
出处
期刊:Nature Energy
[Springer Nature]
日期:2025-09-04
卷期号:10 (10): 1205-1214
被引量:1
标识
DOI:10.1038/s41560-025-01847-0
摘要
Abstract Avoiding lithium dendrites at the lithium/ceramic electrolyte interface and, as a result, avoiding cell short circuit when plating at practical current densities remains a significant challenge for all-solid-state batteries. Typically, values are limited to around 1 mA cm −2 , even, for example, for garnets with a relative density of >99%. It is not obvious that simply densifying ceramic electrolytes will deliver high plating currents. Here we show that plating currents of 9 mA cm −2 can be achieved without dendrite formation, by densifying argyrodite, Li 6 PS 5 Cl, to 99%. Changes in the microstructure of Li 6 PS 5 Cl on densification from 83 to 99% were determined by focused ion beam-scanning electron microscopy tomography and used to calculate their effect on the critical current density (CCD). Modelling shows that not all changes in microstructure with densification act to increase CCD. Whereas smaller pores and shorter cracks increase CCD, lower pore population and narrower cracks act to decrease CCD. Calculations show that the former changes dominate over the latter, predicating an overall increase in CCD, as observed experimentally.
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