预聚物
电解质
离子电导率
乙二醇
膜
高分子化学
电化学
材料科学
聚合物
丁二腈
锂(药物)
化学工程
化学
电极
有机化学
物理化学
复合材料
医学
生物化学
工程类
聚氨酯
内分泌学
作者
Ruixuan He,Mauricio Echeverri,Daniel Ward,Yu Zhu,Thein Kyu
标识
DOI:10.1016/j.memsci.2015.10.008
摘要
Abstract The present article demonstrates the effects of molecular weight of network precursor on properties of solid-state polymer electrolyte membrane (PEM) comprised of poly (ethylene glycol) diacrylate (PEGDA) prepolymer, succinonitrile (SCN) plasticizer, and lithium bis (trifluoromethane sulphonyl) imide (LiTFSI) salt using two different PEGDA molecular weights. To provide guidance for crosslinking reaction, ternary phase diagrams of the PEM precursor mixtures were established. Upon photopolymerization within the wide isotropic region, completely amorphous membranes were obtained in several compositions. The PEM having a higher PEGDA molecular weight (i.e., 6000 g/mol) revealed both improved impact strength with an elongation at break of ~80 % and higher ambient temperature ionic conductivity (~1.4×10 −3 S cm −1 ) relative to the low molecular weight counterpart (i.e., 700 g/mol). Both PEMs exhibited excellent electrochemical (4.8 V/Li/Li + ) and thermal (140 °C) stabilities. Specific discharge capacities of the PEM containing half-cells using LiFePO 4 or Li 4 Ti 5 O 12 electrodes against lithium electrode reached the level of ~140 mAh g −1 at 0.2 °C, indicating potential applications in all solid-state lithium-ion batteries.
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