电解质
二甲醚
锂(药物)
二甲氧基乙烷
化学工程
化学
离子电导率
电池(电)
离子液体
乙二醇
微型多孔材料
无机化学
材料科学
有机化学
甲醇
电极
物理化学
功率(物理)
催化作用
内分泌学
工程类
物理
医学
量子力学
作者
Jaewon Choi,Jinkyu Kim,Gouri Cheruvally,Jou‐Hyeon Ahn,Hyo‐Jun Ahn,Ki-Won Kim
标识
DOI:10.1016/j.electacta.2006.08.016
摘要
The suitability of some single/binary liquid electrolytes and polymer electrolytes with a 1 M solution of LiCF3SO3 was evaluated for discharge capacity and cycle performance of Li/S cells at room temperature. The liquid electrolyte content in the cell was found to have a profound influence on the first discharge capacity and cycle property. The optimum, stable cycle performance at about 450 mAh g−1 was obtained with a medium content (12 μl) of electrolyte. Comparison of cycle performance of cells with tetra(ethylene glycol)dimethyl ether (TEGDME), TEGDME/1,3-dioxolane (DIOX) (1:1, v/v) and 1,2-dimethoxyethane (DME)/di(ethylene glycol)dimethyl ether (DEGDME) (1:1, v/v) showed better results with the mixed electrolytes based on TEGDME. The addition of 5 vol.% of toluene in TEGDME had a remarkable effect of increasing the initial discharge capacity from 386 to 736 mAh g−1 (by >90%) and stabilizing the cycle properties, attributed to the reduced lithium metal interfacial resistance obtained for the system. Polymer electrolyte based on microporous poly(vinylidene fluoride) (PVdF) membrane and TEGDME/DIOX was evaluated for ionic conductivity at room temperature, lithium metal interfacial resistance and cycle performance in room-temperature Li/S cells. A comparison of the liquid electrolyte and polymer electrolyte showed a better performance of the former.
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