Ye Guo, Hong Xufeng, He Mengxue, Song Junjie, Zhu Lujun, Zheng Chengxi, Ma Yue, An Yun, Shen Kaier, Shi Weize, Jia Yongfeng, Shafqat Muhammad Burhan, Gao Peng, Xia Dingguo, Chen Fangfang, Pang Quanquan
Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Adv Mater. 2025 Mar;37(12):e2417829. doi: 10.1002/adma.202417829. Epub 2025 Feb 18.
Solid polymer electrolytes (SPEs) are promising for high-energy and high-safety solid-state lithium metal batteries (LMBs). Here, a polycationic solid electrolyte (PCSE) is described that leverages the inherent high thermal/chemical stability of the polycationic domain and the anion trapping (FMAT) effect of another fluorinated microdomain for stable and fast-charging high-voltage LMBs. Specifically, while the polycationic imidazolium backbone ensures high segmental flexibility facilitating the Li mobility, the fluorinated microdomain effectively traps the bis(trifluoromethanesulfonyl)imide anions by strong dipole interactions, imparting localized solvation and restricted mobility of the anions, as well as improved oxidation stability. As a result, the PCSE exhibits a high ionic conductivity of 1.4 mS cm, a high Li transference number of 0.50, and a wide electrochemical window of ∼5.5 V at 25 °C. By way of in situ thermal polymerization of the electrolyte within assembled cells, the PCSE enables ultra-stable cycling of Li|LiNiCoMnO cells with a capacity retention of 98.1% after 500 cycles at 0.2 C at ambient temperatures. The work on the molecular design of PCSEs represents a fundamentally unique perspective for the rational design of SPEs with balanced properties that are historically challenging for high-energy, long-life, ambient-temperature solid-state LMBs.
固态聚合物电解质(SPEs)对于高能和高安全性的固态锂金属电池(LMBs)具有广阔前景。在此,描述了一种聚阳离子固体电解质(PCSE),它利用聚阳离子域固有的高热稳定性/化学稳定性以及另一个氟化微域的阴离子捕获(FMAT)效应,实现稳定且快速充电的高压LMBs。具体而言,聚阳离子咪唑鎓主链确保了高链段柔性,有利于锂离子迁移,而氟化微域通过强偶极相互作用有效地捕获双(三氟甲磺酰)亚胺阴离子,赋予阴离子局部溶剂化和受限迁移率,以及提高的氧化稳定性。结果,PCSE在25℃下表现出1.4 mS cm的高离子电导率、0.50的高锂迁移数和约5.5 V的宽电化学窗口。通过在组装电池内对电解质进行原位热聚合,PCSE可实现Li|LiNiCoMnO电池的超稳定循环,在室温下以0.2 C进行500次循环后容量保持率为98.1%。关于PCSE分子设计的这项工作为合理设计具有平衡性能的SPEs提供了一个从根本上独特的视角,而这些性能对于高能、长寿命、室温固态LMBs来说历来具有挑战性。