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Stabilized Electrode/Electrolyte Interphase by a Saturated Ionic Liquid Electrolyte for High-Voltage NMC532/Si-Graphite Cells

机译:稳定电极/电解质通过饱和离子液体电解质与高压NMC532 / Si-石墨细胞相互作用

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摘要

Nonaqueous electrolyte has become one of the technical barriers in enabling Li-ion battery comprising of a high voltage cathode and high capacity anode. In this work, we demonstrate a saturated piperidinum bis(fluorosulfonyl)imide ionic liquid (IL) with a LiFSI salt not only supports the redox reaction on the cathode at high voltages, but also shows exceptional kinetic stability on the lithiated anode as evidenced by its improved cycling performance in a NMC532/Si-graphite full cells cycled between 4.6 and 3.0 V. On the basis of the spectroscopic/microscopic analysis and molecular dynamics (MD) simulations, the superior performance of the cells is attributed to the formation of solid-electrolyte-interphase on both electrode as well as unique solvation structure where a deadlocked coordination network is established at the saturated state, which prevents transition metal dissolution into the electrolyte via a solvation process.
机译:非水电解质已成为使锂离子电池的技术障碍之一,包括高压阴极和高容量阳极。 在这项工作中,我们证明了一种饱和哌啶双(氟磺酰基)酰亚胺离子液体(IL),其中Lifsi盐不仅在高电压下支持阴极上的氧化还原反应,而且在锂化阳极上显示出卓越的动力学稳定性,如其所示 在4.6和3.0 V之间循环的NMC532 / Si-Graphite全细胞中改善了循环性能。基于光谱/微观分析和分子动力学(MD)模拟,细胞的优异性能归因于形成固体 - 在饱和状态下建立僵化的配位网络的电极上的电解质相互作用以及独特的溶剂化结构,其防止过渡金属溶解在电解质中通过溶剂化方法进入电解质。

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