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首页> 外文期刊>Electrochimica Acta >Elucidating Oligomer-Surface and Oligomer-Oligomer Interactions at a Lithiated Silicon Surface
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Elucidating Oligomer-Surface and Oligomer-Oligomer Interactions at a Lithiated Silicon Surface

机译:阐明锂硅表面上的低聚物-表面和低聚物-低聚物相互作用

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Solid-electrolyte interphase (SEI) layers are multicomponent films formed at the surface of electrodes in Li-ion batteries due to electrochemical instability of the electrolyte components. The properties of this film significantly affect the lifetime of the battery. Here we study the interaction of some electrolyte reduction products (oligomers) with a bare Li13Si4 (010) surface and a Li13Si4 (010) surface partially covered with lithium fluoride (LiF) using classical Monte Carlo and density functional theory-based methods The adsorption, charge transfer, and association of oligomers on the surface are reported. Overall, the oligomers attach firmly to the surface. Our findings indicate that the surface-oligomer interaction dominates the stabilization of the system up to a coverage of approximately 1 oligomerm(2) and once this coverage is reached, oligomer-oligomer interactions dominate the stabilization of the porous block. Regarding association, lithium ethylene dicarbonate (Li2EDC) tends to associate with the bare and partially covered surface through O.Li.O bridges. However, the association mechanism varies depending on the existing nucleating products at the surface. In contrast, lithium vinylene dicarbonate (Li2VDC)'s backbone is closer to the surface and exhibits a more flexible structure than the Li2EDC oligomer. This difference may further affect the compactness of the SEI layer. Aligned with our previous studies, we also found oligomer decomposition on the surface. Our calculations offer critical information regarding the structure of electrolyte decomposition products over silicon electrodes. (C) 2016 Elsevier Ltd. All rights reserved.
机译:固体电解质相间(SEI)层是由于电解质组分的电化学不稳定性而在锂离子电池中的电极表面形成的多组分膜。该薄膜的性能会显着影响电池的使用寿命。在这里,我们使用经典的蒙特卡洛方法和基于密度泛函理论的方法研究了一些电解质还原产物(低聚物)与裸露的Li13Si4(010)表面和部分覆盖有氟化锂(LiF)的Li13Si4(010)表面的相互作用。报告了电荷转移和表面上低聚物的缔合。总体而言,低聚物牢固地附着在表面上。我们的发现表明,表面-低聚物相互作用主导了系统的稳定性,覆盖率约为1个低聚物/ nm(2),一旦达到该覆盖率,低聚物-低聚物相互作用就主导了多孔嵌段的稳定性。关于缔合,碳酸二亚乙酯锂(Li2EDC)倾向于通过O.Li.O桥与裸露和部分覆盖的表面缔合。但是,缔合机理取决于表面上现有的成核产物。相比之下,碳酸亚乙烯锂(Li2VDC)的主链更靠近表面,并且比Li2EDC低聚物显示出更灵活的结构。这种差异可能会进一步影响SEI层的紧凑性。与我们以前的研究一致,我们还发现了表面上的低聚物分解。我们的计算提供了有关硅电极上电解质分解产物结构的关键信息。 (C)2016 Elsevier Ltd.保留所有权利。

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