枝晶(数学)
材料科学
电解质
脆性
渗透(战争)
复合材料
锂(药物)
纳米尺度
快离子导体
电子显微镜
剪切(地质)
相间
脆性断裂
扫描电子显微镜
纳米技术
剪应力
蠕动
压力(语言学)
作者
Qing Ai,B. Zhang,Xing Liu,Bongki Shin,Wenhua Guo,Guanhui Gao,Lihong Zhao,Xintong Weng,Qiyi Fang,Tianshu Zhai,Doug Steinbach,Yifan Zhu,Yifeng Liu,Fan Wang,Xiaoyin Tian,Hua Guo,Youtian Zhang,Xuan Zhao,Yimo Han,Ming Tang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-03-12
卷期号:391 (6790): 1125-1129
被引量:8
标识
DOI:10.1126/science.adu9988
摘要
The growth and penetration of lithium dendrites through electrolytes and separators remain key challenges to realizing high-energy density lithium-metal batteries. Using mechanically strong electrolytes and separators has been considered a promising strategy based on the commonly believed softness of lithium. However, dendrite formation persists in stiff solid electrolytes, suggesting distinct mechanical behaviors. We measured the mechanical properties of individual lithium dendrites using an air-free protocol. We found that lithium dendrites are unexpectedly strong and brittle, with fracture stress greater than ~150 megapascals, unlike the ductile bulk metal. Cryo-transmission electron microscopy and mechanical modeling showed that this behavior arises from solid electrolyte interface constraints and nanoscale strengthening. These findings provide alternative mechanisms for dendrite penetration and dead lithium formation as well as guidance for design strategies for lithium-metal batteries.
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