材料科学
聚合物
锂(药物)
硫黄
电池(电)
石墨烯
化学工程
锂硫电池
纳米技术
复合材料
功率(物理)
冶金
内分泌学
工程类
物理
医学
量子力学
作者
Borui Li,Wanyuan Jiang,Yunpeng Qu,Wenhai Song,Xin Jin,Mengfan Pei,Shuo Zhuo,Runyue Mao,Lin Wang,Dongming Liu,Xigao Jian,Fangyuan Hu
标识
DOI:10.1002/adma.202503482
摘要
Abstract Achieving stable operation under a wide temperature range is a critical target for the practical applications of lithium–sulfur batteries. However, intense lithium polysulfides (LiPSs) shuttling at high‐temperature, sluggish sulfur species conversion, and inhomogeneous Li + deposition at low‐temperature severely impair the cycle lifespan of batteries. Herein, the multifunctional polymer brushes are fabricated by grafting anthraquinone‐functionalized poly(glycidyl methacrylate) brushes on graphene surfaces (G‐pGMAAQ) to simultaneously regulate the evolution of sulfur and lithium species. Combining theoretical calculations and experiments, it is revealed that G‐pGMAAQ serves as a redox mediator that reduces the LiPSs conversion energy barrier, and its unique polar brush‐like structure effectively inhibits LiPSs shuttling and homogenizes Li + flow. Hence, G‐pGMAAQ facilitates lithium–sulfur batteries stable operation in an ultra‐wide temperature range (−40–70 °C). Furthermore, the Ah‐level pouch cell achieves an energy density of 417 Wh kg −1 , demonstrating the commercial potential of polymer brushes for lithium–sulfur batteries.
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