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Resolving Heterogeneity in Battery Interphases By Cryogenic Electron Microscopy

机译:通过低温电子显微镜解决电池间晶体中的异质性

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The stability of lithium batteries is tied to the physicochemical properties of the solid-electrolyte interphase (SEI), a surface passivation layer on the battery anode. However, owing to the difficulty in characterizing this sensitive interphase with nanoscale resolution, the distribution of SEI components at the nanoscale is poorly understood. Here, we use cryogenic scanning transmission electron microscopy (cryo-STEM) and electron energy loss spectroscopy (EELS) to map the spatial distribution of sensitive SEI components across the metallic Li anode. We reveal that LiF, an inorganic SEI component widely believed to play an important role in battery passivation, is absent within the compact SEI film (~15 nm) in direct contact with the active material. Instead, LiF particles (100-400 nm) are found to precipitate across the electrode surface independently from compact SEI formation. Based on these observations, we conclude that LiF cannot be a dominant contribution to anode passivation nor does it influence Li~+ transport across the compact SEI film. Using cryo-STEM and EELS, we refine the traditional view of the SEI structure derived from ensemble-averaged characterizations and nuance the role of SEI components on battery performance.
机译:锂电池的稳定性与电池阳极上的固体电解质间(SEI)的物理化学性质相关联。然而,由于难以表征与纳米级分辨率的这种敏感性相互作用,纳米级在纳米级的分布很差。这里,我们使用低温扫描透射电子显微镜(Cryo-Step)和电子能量损失光谱(EEL)来映射在金属锂阳极上的敏感SEI组件的空间分布。我们揭示了LIF,一种广泛认为在电池钝化中发挥重要作用的无机SEI成分,在紧凑的SEI膜(〜15nm)内不存在与活性材料直接接触。相反,发现LiF颗粒(100-400nm)独立于紧凑的SEI形成,以独立地沉淀到电极表面上。基于这些观察结果,我们得出结论,LIF不能成为对阳极钝化的主导贡献,也不会影响锂+在紧凑的SEI膜上的运输。使用Cryo-Stew和EELS,我们优化SEI结构的传统观点,从集合平均表征和NUICE中的角色源于SEI组件对电池性能的影响。

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