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用于提升高安全性和宽温度锂金属电池性能的复合固态电解质界面-凝胶电解质原位集成设计

In situ integrated design of composite SEI-gel electrolytes boosting high-safety and wide-temperature lithium metal batteries.

作者信息

Song Fuchen, Zhao Lijun, Yan Junmin

机构信息

Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.

Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.

出版信息

J Colloid Interface Sci. 2026 Jan 15;702(Pt 1):138907. doi: 10.1016/j.jcis.2025.138907. Epub 2025 Sep 1.

DOI:10.1016/j.jcis.2025.138907
PMID:40912012
Abstract

Neither single electrolyte design nor solid electrolyte interface (SEI) engineering alone can effectively resolve the dual challenges of sluggish reaction kinetics and unstable interfaces in polymer-based lithium metal batteries (LMBs). Herein, a rational integrated design strategy is adopted to simultaneously fabricate poly(trifluoroethyl methacrylate-co-4-oxo-5,8,11-trioxa-3-azatridec-12-en-1-yl acrylate)-based gel polymer electrolyte (PTDA-GPE) and stable composite SEI during the thermal-induced in situ polymerization process. The resulting PTDA-GPE demonstrates superior Li transport kinetics (1.34 mS cm at 30 °C), enhanced mechanical strength and flame retardancy, and an expanded electrochemical window of up to 4.8 V (vs. Li/Li). Notably, the SEI constructed using the differentiated adsorption forces and redox kinetics between various components and lithium metal has a unique organic-inorganic composite structure. Ultimately, Li/PTDA-GPE/LiFePO batteries can achieve over 1000 stable cycles at -20 °C and 60 °C (capacity retention of 95 % and 80 %, respectively),and Li/PTDA-GPE/LiCoO demonstrates high capacity retention of 98 % after 200 cycles. In addition, the 1.2 Ah Li/PTDA-GPE/LiFePO pouch cell can guarantee enhanced safety features and constant output voltage under abuse conditions. This work demonstrates a facile and universal strategy for in situ integrated fabrication of composite SEI/GPE.

摘要

单独的单一电解质设计或固体电解质界面(SEI)工程都无法有效解决聚合物基锂金属电池(LMBs)中反应动力学迟缓以及界面不稳定这两个双重挑战。在此,我们采用了一种合理的集成设计策略,在热诱导原位聚合过程中同时制备基于聚(甲基丙烯酸三氟乙酯 - 共 - 4 - 氧代 - 5,8,11 - 三氧杂 - 3 - 氮杂十三碳 - 12 - 烯基丙烯酸酯)的凝胶聚合物电解质(PTDA - GPE)和稳定的复合SEI。所得的PTDA - GPE表现出优异的Li传输动力学(30°C时为1.34 mS cm)、增强的机械强度和阻燃性,以及高达4.8 V(相对于Li/Li)的扩展电化学窗口。值得注意的是,利用各种成分与锂金属之间不同的吸附力和氧化还原动力学构建的SEI具有独特的有机 - 无机复合结构。最终,Li/PTDA - GPE/LiFePO电池在 - 20°C和60°C下可实现超过1000次稳定循环(容量保持率分别为95%和80%),并且Li/PTDA - GPE/LiCoO在200次循环后表现出98%的高容量保持率。此外,1.2 Ah的Li/PTDA - GPE/LiFePO软包电池在滥用条件下能够保证增强的安全性能和恒定的输出电压。这项工作展示了一种用于复合SEI/GPE原位集成制备的简便通用策略。

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