电解质
盐(化学)
锂(药物)
环氧乙烷
离子
聚合物
无定形固体
分子动力学
离子键合
材料科学
无机化学
化学
化学工程
化学物理
物理化学
有机化学
计算化学
内分泌学
工程类
医学
电极
共聚物
作者
Nicola Molinari,Jonathan P. Mailoa,Boris Kozinsky
标识
DOI:10.1021/acs.chemmater.8b01955
摘要
Currently available solid polymer electrolytes for Li-ion cells require deeper understanding and significant improvement in ionic transport properties to enable their use in high-power batteries. We use molecular dynamics simulations to model the solid amorphous polymer electrolyte system comprising poly(ethylene) oxide (PEO), lithium, and bis(trifluoromethane)sulfonimide anion (TFSI), exploring effects of high salt concentrations relevant for battery applications. Using statistical analysis of ion distribution and transport, we investigate the significant effect that salt concentration has on ion mobility. At practical salt concentrations, a previously undetected ensemble of Li–TFSI clusters emerges where Li ions have significantly lower coordination by the polymer, and this results in their significantly lower mobility as compared to Li ions coordinated by the polymer. We also find the tendency for cation–anion clusters to be asymmetrical, with the anions in greater number than Li cations, which may further affect the transport properties of this material. The existence of such negatively charged clusters has been recently speculated to explain the experimentally observed negative transference number at high LiTFSI concentrations in PEO. Our methodology enables us to suggest strategies for improvement of transport properties and can be generalized to other polymer–Li–salt combinations.
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