Department of Chemical and Materials Engineering, University of Kentucky , Lexington, Kentucky 40506-0046, United States.
Chemical Sciences and Materials Systems Laboratory, General Motors Global Research and Development Center , Warren, Michigan 48090-9055, United States.
ACS Appl Mater Interfaces. 2016 Mar 2;8(8):5687-93. doi: 10.1021/acsami.5b12030. Epub 2016 Feb 18.
Understanding of the electrical conduction, that is, ionic and electronic conduction, through the solid electrolyte interphase (SEI) is critical to the design of durable lithium-ion batteries (LIBs) with high rate capability and long life. It is believed that an ideal SEI should not only be an ionic conductor, but also an electronic insulator. In this study, we present a theoretical design of an artificial SEI consisting of lithium fluoride (LiF) and lithium carbonate (Li2CO3) on a LIB anode based on a newly developed density functional theory (DFT) informed space charge model. We demonstrate that the migration of lattice Li ions from LiF phase to form Li interstitials in Li2CO3 is energetically favorable near the LiF/Li2CO3 interface. At equilibrium, this interfacial defect reaction establishes a space charge potential across the interface, which causes the accumulation of ionic carriers but the depletion of electronic carriers near the LiF/Li2CO3 interface. To utilize this space charge effect, we propose a computationally designed, nanostructured artificial SEI structure with high density of interfaces of LiF and Li2CO3 perpendicular to the electrode. On the basis of this structure, the influences of grain size and volume ratio of the two phases were studied. Our results reveal that reducing the grain size of Li2CO3 in the nanostructured composite can promote ionic carriers and increase the ionic conductivity through the composite SEI by orders of magnitude. At the same time, the electronic conductivity is reduced due to electron depletion near the LiF/Li2CO3 interface. Furthermore, an optimal volume fraction that ensures high ionic and low electronic conduction was predicted.
理解固体电解质界面相(SEI)的电传导,即离子和电子传导,对于设计具有高倍率能力和长寿命的耐用锂离子电池(LIB)至关重要。人们认为,理想的 SEI 不仅应该是离子导体,而且应该是电子绝缘体。在这项研究中,我们基于新开发的密度泛函理论(DFT)告知的空间电荷模型,提出了一种由氟化锂(LiF)和碳酸锂(Li2CO3)组成的人工 SEI 的理论设计,用于 LIB 阳极。我们证明,晶格 Li 离子从 LiF 相迁移到 Li2CO3 中形成 Li 间隙在 LiF/Li2CO3 界面附近是能量有利的。在平衡时,这种界面缺陷反应在界面上建立了一个空间电荷电势,导致在 LiF/Li2CO3 界面附近离子载流子的积累和电子载流子的耗尽。为了利用这种空间电荷效应,我们提出了一种计算设计的、具有高密度 LiF 和 Li2CO3 界面的纳米结构人工 SEI 结构,这些界面垂直于电极。在此结构的基础上,研究了两种相的晶粒尺寸和体积比的影响。我们的结果表明,减小纳米结构复合材料中 Li2CO3 的晶粒尺寸可以通过数量级促进离子载流子并增加通过复合 SEI 的离子电导率。同时,由于 LiF/Li2CO3 界面附近的电子耗尽,电子电导率降低。此外,预测了确保高离子和低电子传导的最佳体积分数。