锂(药物)
电解质
金属锂
固态核磁共振
核磁共振波谱
金属
硫化物
材料科学
光谱学
化学
化学工程
电极
核磁共振
物理化学
立体化学
冶金
物理
工程类
内分泌学
医学
量子力学
作者
Ziteng Liang,Yuxuan Xiang,Kangjun Wang,Jianping Zhu,Yanting Jin,Hongchun Wang,Bizhu Zheng,Zirong Chen,Mingming Tao,Xiangsi Liu,Yuqi Wu,Riqiang Fu,Chunsheng Wang,Martin Winter,Yong Yang
标识
DOI:10.1038/s41467-023-35920-7
摘要
The performance of all-solid-state lithium metal batteries (SSLMBs) is affected by the presence of electrochemically inactive (i.e., electronically and/or ionically disconnected) lithium metal and solid electrolyte interphase (SEI), which are jointly termed inactive lithium. However, the differentiation and quantification of inactive lithium during cycling are challenging, and their lack limits the fundamental understanding of SSLMBs failure mechanisms. To shed some light on these crucial aspects, here, we propose operando nuclear magnetic resonance (NMR) spectroscopy measurements for real-time quantification and evolution-tracking of inactive lithium formed in SSLMBs. In particular, we examine four different sulfide-based solid electrolytes, namely, Li10GeP2S12, Li9.54Si1.74P1.44S11.7Cl0.3, Li6PS5Cl and Li7P3S11. We found that the chemistry of the solid electrolyte influences the activity of lithium. Furthermore, we demonstrate that electronically disconnected lithium metal is mainly found in the interior of solid electrolytes, and ionically disconnected lithium metal is found at the negative electrode surface. Moreover, by monitoring the Li NMR signal during cell calendar ageing, we prove the faster corrosion rate of mossy/dendritic lithium than flat/homogeneous lithium in SSLMBs.
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