Boosting(机器学习)
电解质
金属锂
材料科学
乙醚
聚合物
电池(电)
锂电池
聚合物电解质
锂(药物)
化学工程
无机化学
化学
有机化学
计算机科学
复合材料
工程类
离子键合
离子
电极
离子电导率
人工智能
物理
心理学
功率(物理)
物理化学
量子力学
精神科
作者
Chenchen Zhang,Zuohang Li,Su Wang,Li Chen,Yuchang Si,Yue Ma,Dawei Song,Hongzhou Zhang,Xixi Shi,Lianqi Zhang
标识
DOI:10.34133/energymatadv.0188
摘要
Ether-based electrolytes are widely used in lithium metal batteries owing to their higher compatibility with Li anodes compared to that of carbonate-based electrolytes. Compared to the concern with high voltage resistance characteristics, little attention has been paid to Li-ion transportation in ether-based systems. Hence, a 1,2-dimethoxyethane-based poly(methyl methacrylate-ethoxylated trimethylolpropane triacrylate) gel polymer electrolyte (named ME-GPE) was developed to realize rapid Li-ion transfer and construct compatible interfaces. The LiFePO 4 /ME-GPE/Li battery presents a high-rate (10 C) capacity retention of 85.6% after 200 cycles, while sluggish Li-ion transfer is exhibited in the liquid counterpart and a low capacity retention of 47.2% is presented after cycling. Density functional theory calculations show that the binding energies of Li + /DFOB − with a polymer matrix are much higher than those of the liquid electrolyte, which is conducive to the release and the rapid transfer of more Li ions. 7 Li solid-state nuclear magnetic resonance exhibits a similar result; the higher frequency observed after cycling indicates a larger electron density variation and greater mobility of Li ions. Moreover, the interfacial characteristics were investigated, and Li-ion plating/stripping behaviors are regulated by abundant polar groups on polymers. Therefore, rapid Li-ion transfer capability and outstanding interface stability were simultaneously achieved for ether-based systems for the first time.
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