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In Situ Observation of Electrolyte-Concentration-Dependent Solid Electrolyte Interphase on Graphite in Dimethyl Sulfoxide

机译:二甲基亚砜中石墨上电解质浓度依赖性固体电解质界面的原位观察

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摘要

High lithium salt concentration strategy has been recently reported to be an effective method to enable various organic solvents as electrolyte of batteries. Here, we utilize in situ atomic force microscopy (AFM) to investigate the interfacial morphology on the graphite electrode in dimethyl sulfoxide (DMSO)-based electrolyte of various concentrations. The significant differences in interfacial features of the graphite in electrolytes of different concentrations. are revealed. In the concentrated electrolyte, stable films form primarily at the step edges and defects on the graphite surface after initial electrochemical cycling. On the other hand, in the dilute electrolyte; DMSO-solvated lithium ions constantly intercalate into graphite layers, and serious decomposition of solvent accompanied by structural deterioration of the graphite surface is observed. The in situ AFM results provide direct evidence for the concentration-dependent interface reactions between graphite electrode and DMSO-based electrolyte.
机译:最近已经报道了高锂盐浓度策略是使各种有机溶剂能够用作电池电解质的有效方法。在这里,我们利用原位原子力显微镜(AFM)来研究各种浓度的基于二甲基亚砜(DMSO)的电解液中石墨电极上的界面形态。在不同浓度的电解质中,石墨的界面特征存在显着差异。被揭示。在浓电解液中,最初的电化学循环后,稳定的膜主要形成在台阶边缘和石墨表面的缺陷处。另一方面,在稀电解质中; DMSO溶剂化的锂离子不断插入到石墨层中,并且观察到溶剂的严重分解,同时石墨表面的结构变差。原位原子力显微镜的结果为石墨电极与DMSO基电解质之间的浓度依赖性界面反应提供了直接证据。

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