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确定固体电解质界面持续生长的机制。

Identifying the Mechanism of Continued Growth of the Solid-Electrolyte Interphase.

作者信息

Single Fabian, Latz Arnulf, Horstmann Birger

机构信息

German Aerospace Center (DLR), Pfaffenwaldring 38-40, 70569, Stuttgart, Germany.

Helmholtz Institute Ulm (HIU), Helmholtzstraße 11, 89081, Ulm, Germany.

出版信息

ChemSusChem. 2018 Jun 22;11(12):1950-1955. doi: 10.1002/cssc.201800077. Epub 2018 Apr 17.

Abstract

Continued growth of the solid-electrolyte interphase (SEI) is the major reason for capacity fade in modern lithium-ion batteries. This growth is made possible by a yet unidentified transport mechanism that limits the passivating ability of the SEI towards electrolyte reduction. We, for the first time, differentiate the proposed mechanisms by analyzing their dependence on the electrode potential. Our calculations are compared to recent experimental capacity-fade data. We show that the potential dependence of SEI growth facilitated by solvent diffusion, electron conduction, or electron tunneling qualitatively disagrees with the experimental observations. Only diffusion of Li interstitials results in a potential dependence matching the experiments. Therefore, we identify the diffusion of neutral radicals, such as Li interstitials, as the cause of long-term SEI growth.

摘要

固体电解质界面(SEI)的持续生长是现代锂离子电池容量衰减的主要原因。这种生长是由一种尚未明确的传输机制促成的,该机制限制了SEI对电解质还原的钝化能力。我们首次通过分析所提出的机制对电极电位的依赖性来区分它们。我们的计算结果与最近的实验容量衰减数据进行了比较。我们表明,由溶剂扩散、电子传导或电子隧穿促进的SEI生长的电位依赖性与实验观察结果在定性上不一致。只有锂间隙原子的扩散导致的电位依赖性与实验相匹配。因此,我们确定中性自由基(如锂间隙原子)的扩散是SEI长期生长的原因。

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