High-Throughput Screening Lithium Alloy Phases and Investigation of Ion Transport for Solid Electrolyte Interphase Layer

IF 13.5 2区 化学 Q1 CHEMISTRY, PHYSICAL 物理化学学报 Pub Date : 2024-03-01 Epub Date: 2023-07-18 DOI:10.3866/PKU.WHXB202305039
Zhi Dou, Huiyu Duan, Yixi Lin, Yinghui Xia, Mingbo Zheng, Zhenming Xu
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Abstract

Solid electrolyte interphase (SEI) layers derived from the side reactions between Li metal anode and electrolyte, have great impacts on the electrochemical performance of lithium batteries. In solid-state batteries, SEI layers are also required as the electrical insulators but an ionic conductors, and the mechanical reinforcements for withstanding volume change and suppressing dendritic growth in Li metal anode. Introducing LiF substrates into SEI layers can significantly reduce the electron tunneling ability from Li anode to SEI layer, meanwhile providing the excellent interfacial mechanical strength. However, LiF has a very high energy barrier for ion diffusion, hindering the rapid lithium ion diffusion from SEI layer to lithium anode. Therefore, it is necessary to introduce lithium alloy phases with higher ionic conductivity into the LiF matrix to provide sufficient ion diffusion channels. By the data mining technology, high-throughput first-principle calculation and ab-initio molecular dynamics simulations, this work performed phase diagram and ion diffusion energy barrier calculations to evaluate the thermodynamic stabilities and lithium diffusion abilities of several lithium alloys. 27 lithium alloys that can be used as Li-ion conducting phases in the LiF-based artificial SEI layers are screened. Meanwhile, the structure-function relationship analysis of lithium alloys uncovers that the crystal structure type of lithium alloys has more significant impacts on lithium ion diffusion than alloy elements, that is, lithium alloy structures with the space group of I 4¯3d and Fm 3¯m have very excellent lithium ion transport performance, while the diffusion channels of lithium alloy structures with the space group of Pm 3¯m and F4 3¯m are narrow, leading to the poor lithium ion transport performance. In addition, this work uncovers a physical image of lithium ion transport in artificial SEI interface, that is, lithium ion diffusion in LiF crystal bulk is quite difficult, while the diffusion resistance at LiF grain boundaries and LiF/LiM alloy interfaces is small.
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高通量筛选锂合金相及固体电解质相间层离子传输研究
固体电解质间相(SEI)层是由锂金属阳极与电解质之间的副反应产生的,对锂电池的电化学性能有很大影响。在固态电池中,SEI层也需要作为电绝缘体和离子导体,以及在Li金属阳极中承受体积变化和抑制枝晶生长的机械增强。在SEI层中引入LiF衬底可以显著降低Li阳极到SEI层的电子隧穿能力,同时提供优异的界面机械强度。然而,LiF具有很高的离子扩散能垒,阻碍了锂离子从SEI层向锂阳极的快速扩散。因此,有必要在LiF基体中引入离子电导率较高的锂合金相,以提供充足的离子扩散通道。通过数据挖掘技术、高通量第一性原理计算和从头算分子动力学模拟,对几种锂合金的热力学稳定性和锂扩散能力进行了相图和离子扩散能垒计算。筛选了27种可作为锂离子导电相的锂合金。同时,对锂合金的结构-功能关系分析发现,锂合金的晶体结构类型对锂离子扩散的影响比合金元素更显著,即空间群为I4¯3d和Fm3¯m的锂合金结构具有非常优异的锂离子输运性能,而空间群为Pm3¯m和F43¯m的锂合金结构的扩散通道狭窄。导致锂离子输运性能差。此外,本工作揭示了锂离子在人工SEI界面中输运的物理图像,即锂离子在LiF晶体体中的扩散相当困难,而在LiF晶界和LiF/LiM合金界面处的扩散阻力很小。下载:下载高清图片(60KB)下载:下载全尺寸图片
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来源期刊
物理化学学报
物理化学学报 化学-物理化学
CiteScore
16.60
自引率
5.50%
发文量
9754
审稿时长
1.2 months
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