Bingyu Lu1,Wei-Kang Li1,Diyi Cheng1,Bhargav Bhamwala1,Miguel Ceja1,Wuriguluma Bao1,Chengcheng Fang2,Y. Shirley Meng3
University of California, San Diego1,Michigan State University2,The University of Chicago3
Bingyu Lu1,Wei-Kang Li1,Diyi Cheng1,Bhargav Bhamwala1,Miguel Ceja1,Wuriguluma Bao1,Chengcheng Fang2,Y. Shirley Meng3
University of California, San Diego1,Michigan State University2,The University of Chicago3
The lithium (Li) metal anode is essential for next generation high energy density rechargeable Li metal batteries. Although extensive studies have been performed to prolong the cycle life of Li metal batteries, the calendar life, which associates with chemical corrosion of Li metal in liquid electrolytes, has not been quantitatively understood. Here, by combing the Titration Gas Chromatography (TGC) method and Cryogenic Focused Ion Beam (Cryo-FIB), we established a quantitative relationship between the chemical corrosion rate and electrochemically deposited Li morphology in various liquid electrolyte systems. We identified that the corrosion rate is dominated by the porosity of the deposited Li. The larger the porosity of deposited Li has, the faster the corrosion rate will be. We further proposed strategies to mitigate the chemical corrosion on Li thus to extend the calendar life of Li metal batteries. By strictly controlling the stacking pressure during Li plating, Li deposits with ultra-low porosity can be achieved, suppressing the corrosion rate to 0.08 ± 0.16%/day compared with 1.71 ± 0.19%/day of the high-porosity Li.