阳极
微观结构
电解质
材料科学
电流密度
电镀(地质)
陶瓷
扫描电子显微镜
枝晶(数学)
锂(药物)
复合材料
分析化学(期刊)
冶金
化学
电极
医学
几何学
物理
地球物理学
物理化学
数学
量子力学
色谱法
内分泌学
地质学
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
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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