Disentangling Lithium Failure Mechanisms in Liquid Electrolytes by 2D Exchange Solid-State NMR

化学 电解质 锂(药物) 离子键合 离子液体 相间 化学物理 化学工程 法拉第效率 核磁共振波谱 无机化学 金属 金属锂 离子交换 可见的 分析化学(期刊) 表征(材料科学) 化学稳定性 光谱学 二维核磁共振波谱
作者
Zhuo Han,Likun Chen,Chenjie Lou,Yuhang Li,Yongqi Chen,Yubin Li,Weijie Liu,Zhihao Lei,Xufei An,Kun Peng,Jiawang Meng,Ming Liu
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
标识
DOI:10.1021/jacs.6c12458
摘要

Abstract High Coulombic efficiency (CE, >99.9%) for Li plating/stripping is essential for thin-Li and anode-free Li metal batteries, yet understanding Li failure mechanisms remains challenging. Here, we propose a failure analysis method employing two-dimensional exchange solid-state NMR spectroscopy (2D EXSY ssNMR) to define the relative dead Li0/solid electrolyte interphase (SEI) contribution (R(A/B)) and the ratio of SEI-dead Li0 exchange intensity to SEI (R(C/B)). Together, these descriptors link inactive-Li composition with SEI-Li0 exchange, enabling ionic contact failure to be distinguished from electronic contact failure. In ester-based electrolytes, a large R(A/B) indicates dead-Li0-dominated inactive Li loss, while the observable exchange peak suggests that ionic exchange pathways are preserved. The failure is therefore mainly associated with electronic isolation of whisker-like Li deposits. Ether-based (localized) high-concentration electrolytes effectively suppress dead Li0 formation, while decreasing R(C/B) reveals progressively weakened Li exchange across inorganic-rich SEI during extended cycling. Thus, long-term failure in high-CE electrolytes is dominated by ionic contact loss rather than electronically isolated dead-Li0 accumulation, because inorganic-rich SEI lacks sufficient deformability to maintain interfacial contact during repeated volume changes. This process may be further intensified by gradual liquid-electrolyte depletion. Overall, these results establish 2D EXSY ssNMR as a comparative diagnostic tool for Li failure modes and highlight the need for SEI designs that combine chemical stability with mechanical adaptability.
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