电解质
聚合物
材料科学
无定形固体
锂(药物)
化学工程
聚合物电解质
硫黄
离子电导率
无机化学
电极
化学
有机化学
物理化学
内分泌学
工程类
医学
作者
Juan Zhang,Jia Chou,Xiaoxi Luo,Yiming Yang,Ming‐Yan Yan,Jia Di,Chaohui Zhang,Yahui Wang,Wenpeng Wang,Shuang‐Jie Tan,Jun‐Chen Guo,Yao Zhao,Fuyi Wang,Sen Xin,Li‐Jun Wan,Yu‐Guo Guo
标识
DOI:10.1002/anie.202316087
摘要
Abstract Solid‐state lithium‐sulfur batteries have shown prospects as safe, high‐energy electrochemical storage technology for powering regional electrified transportation. Owing to limited ion mobility in crystalline polymer electrolytes, the battery is incapable of operating at subzero temperature. Addition of liquid plasticizer into the polymer electrolyte improves the Li‐ion conductivity yet sacrifices the mechanical strength and interfacial stability with both electrodes. In this work, we showed that by introducing a spherical hyperbranched solid polymer plasticizer into a Li + ‐conductive linear polymer matrix, an integrated dynamic cross‐linked polymer network was built to maintain fully amorphous in a wide temperature range down to subzero. A quasi‐solid polymer electrolyte with a solid mass content >90 % was prepared from the cross‐linked polymer network, and demonstrated fast Li + conduction at a low temperature, high mechanical strength, and stable interfacial chemistry. As a result, solid‐state lithium‐sulfur batteries employing the new electrolyte delivered high reversible capacity and long cycle life at 25 °C, 0 °C and −10 °C to serve energy storage at complex environmental conditions.
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