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设计两性离子刷状聚合物以实现长循环准固态锂金属电池

Designing Zwitterionic Bottlebrush Polymers to Enable Long-Cycling Quasi-Solid-State Lithium Metal Batteries.

作者信息

Li Shimei, Hong Hu, Li Dedi, Yang Xinru, Wang Shixun, Zhang Dechao, Xiong Qi, Huang Zhaodong, Zhi Chunyi

机构信息

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Hong Kong S.A.R., 999077, P. R. China.

Hong Kong Centre for Cerebro-Cardiovascular Health Engineering (COCHE), Shatin, NT, Hong Kong S.A.R., 999077, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2025 Jan 27;64(5):e202409500. doi: 10.1002/anie.202409500. Epub 2024 Dec 16.

Abstract

Ionogel polymer electrolyte (IPE), incorporating ionic liquid (IL) within a polymer matrix, presents a promising avenue for safe quasi-solid-state lithium metal batteries. However, sluggish Li kinetics, resulting from the formation of [Li(anion)] clusters and the occupation of Li transport sites by organic cations, limit their practical applications. In this study, we have developed zwitterionic bottlebrush polymers-based IPE with promoted Li conduction by employing poly(sulfobetaine methacrylate)-grafted poly(vinylidene fluoride-co-chlorotrifluoroethylene) (PVC-g-PSBMA) bottlebrushes as matrices of IL. The grafted zwitterionic side chains greatly facilitate the dissociation of [Li(anion)] clusters to produce more movable Li. Moreover, the positively charged -NR groups in zwitterionic side chains effectively restrain anions migration, while the negatively charged -SO groups immobilize IL cations, preventing them from occupying Li hopping sites and reducing the energy barrier for Li migration. These synergistic effects contribute to a notable ionic conductivity (7.5×10 S cm) and Li transference number (0.62) of PVC-g-PSBMA IPE at 25 °C. As a result, PVC-g-PSBMA IPE enables ultralong-term (over 6500 h) reversible and stable Li plating/stripping in Li||Li symmetric cells. Remarkably, the assembled Li||LiFePO full batteries demonstrate unprecedented cycling stability of more than 2000 cycles with a superior capacity retention of 93.7 %.

摘要

离子凝胶聚合物电解质(IPE)是在聚合物基体中引入离子液体(IL),为安全的准固态锂金属电池提供了一条有前景的途径。然而,由[Li(阴离子)]簇的形成以及有机阳离子占据锂传输位点导致的缓慢锂动力学,限制了它们的实际应用。在本研究中,我们通过使用聚(甲基丙烯酸磺酸甜菜碱)接枝的聚(偏二氟乙烯 - 共 - 氯三氟乙烯)(PVC - g - PSBMA)刷状聚合物作为离子液体的基体,开发了具有促进锂传导性能的两性离子刷状聚合物基IPE。接枝的两性离子侧链极大地促进了[Li(阴离子)]簇的解离,以产生更多可移动的锂。此外,两性离子侧链中带正电的 -NR 基团有效地抑制了阴离子迁移,而带负电的 -SO 基团固定了离子液体阳离子,防止它们占据锂跳跃位点并降低锂迁移的能垒。这些协同效应使得PVC - g - PSBMA IPE在25℃时具有显著的离子电导率(7.5×10 S cm)和锂迁移数(0.62)。结果,PVC - g - PSBMA IPE在Li||Li对称电池中实现了超长期(超过6500 h)的可逆且稳定的锂电镀/剥离。值得注意的是,组装的Li||LiFePO全电池展示了超过2000次循环的前所未有的循环稳定性,具有93.7 %的优异容量保持率。

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