电解质
结晶度
材料科学
锂电池
聚合物
离子电导率
锂(药物)
化学工程
二乙烯基苯
电化学
电导率
电池(电)
高分子化学
无机化学
化学
离子键合
离子
电极
有机化学
复合材料
物理化学
共聚物
苯乙烯
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Hicham Ben Youcef,Oihane García‐Calvo,Nerea Lago,Devaraj Shanmukaraj,Michel Armand
标识
DOI:10.1016/j.electacta.2016.10.122
摘要
Semi-interpenetrated network Solid Polymer Electrolytes (SPEs) were fabricated by UV-induced cross-linking of poly(ethyleneglycol) diacrylate (PEGDA) and divinylbenzene (DVB) within a poly(ethyleneoxide) (PEO) matrix (Mv = 5 × 106 g mol−1), comprising lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI), at a molar ratio of EO:Li ∼ 30:1. The influence of the DVB content on the final SPE properties was investigated in detail. An increase of DVB concentration resulted in self-standing polymer electrolytes. The DVB cross-linker incorporation was found to decrease the crystallinity of the PEO matrix from 34% to 23%, with a decrease in the melting temperature (Tm) of the membrane from 50 °C to 34 °C. Moreover, the influence of the DVB concentration on the ionic conductivity was determined for polymer electrolytes with 0, 10, 20 and 45% DVB from room temperature (RT) to 80 °C. The resulting SPEs showed a high electrochemical stability of 4.3 V as well as practical conductivity values exceeding 10−4 S cm−1 at 70 °C. Cycling performance of these semi-interpenetrated SPE’s have been shown with a Li metal polymer battery and all solid -state Li sulphur battery.
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