快离子导体
离子电导率
电解质
电导率
材料科学
高氯酸锂
离子
离子键合
聚合物
离子运输机
无机化学
化学工程
化学
化学物理
复合材料
有机化学
电极
物理化学
工程类
作者
Shuqi Dai,Jun‐Xia He,Xiupeng Chen,Jinyi Cui,Hongqin Zhao,Rongchun Zhang,Huanyu Lei,Jia‐Fu Yin,Linkun Cai,Fan Ye,Xian Kong,Rongrong Hu,Mingjun Huang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2023-05-02
卷期号:56 (10): 3660-3667
被引量:8
标识
DOI:10.1021/acs.macromol.3c00116
摘要
Polymer electrolytes are considered as solid-state ionic conductors for the next generation of lithium metal batteries. Particularly, poly(ethylene oxide)-based electrolytes have been extensively studied due to their excellent ion conductivity and interfacial compatibility. Since the lithium-ion transport is strongly coupled with segmental motion of polymer chains, there usually exists a dilemma between the ion conductivity and mechanical strength enhancement. Other problems of low ion conductivity at low temperature and low cation transference number further impede their practical applications in batteries. Here, we report a type of polythiourea solid-state electrolyte, which exhibits a superionic ion conducting behavior. The strong supramolecular interaction between the thiourea group and perchlorate anions promotes the dissolution of high concentration lithium salts in polythiourea. The conducting channel composed of high-density thiourea and percolating polar groups enables rapid cation transport along the polymer chain and even working at the glass state. The combined merits of high transference number, good ion conductivity, and excellent mechanical strength are achieved in this class of superionic ionic conductors, shedding light on alternative solutions for solid-state electrolytes in batteries.
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