Dynamics of the extended and intermediate range order in model polymer electrolyte poly(ethylene oxide) and lithium bis(trifluoromethanesulfonyl)imide

P. Falus, A. Faraone, S. Förster, K. Hong, M. Ohl
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Abstract

The dynamics of lithium ions and polymer chains were investigated at the molecular scale in the model polymer electrolyte Poly (ethylene oxide) (PEO)/Lithium bis(trifluoromethanesulfonyl)imide as a function of temperature. This system is known to present an intermediate range order from the arrangement of neighboring chain segments as well as an extended range order of cylindrically arranged chains. The collective dynamics of the systems at lengthscales matching these structural features was measured using Neutron Spin Echo spectroscopy, gaining insights into their lifetime. Moreover, using isotope substitution techniques the dynamics of the lithium ions with respect to the other atoms was probed. The obtained results are compared with the conductivity and the lithium self-diffusion coefficient measured by NMR to gain experimental insight on the molecular processes triggering lithium transport.
模型聚合物电解质聚(环氧乙烷)和双(三氟甲烷磺酰)亚胺锂扩展和中间范围阶的动力学
在分子尺度上研究了聚合物电解质聚环氧乙烷(PEO)/锂二(三氟甲烷磺酰)亚胺中锂离子和聚合物链的动力学随温度的变化。已知该体系从邻近链段的排列呈现出中间范围顺序以及圆柱排列链的扩展范围顺序。利用中子自旋回波光谱测量了与这些结构特征相匹配的系统在长度尺度上的集体动力学,从而深入了解了它们的寿命。此外,利用同位素取代技术,研究了锂离子相对于其他原子的动力学。将所得结果与核磁共振测量的电导率和锂自扩散系数进行比较,以获得对触发锂输运的分子过程的实验见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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