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用于增强锂离子传输动力学的离子凝胶电解质中的竞争性锂配位

Competitive Li Coordination in Ionogel Electrolytes for Enhanced Li-Ion Transport Kinetics.

作者信息

Li Jiafeng, Zhang Tao, Hui Xiaobin, Zhu Ruixiao, Sun Qiqi, Li Xiaoxuan, Yin Longwei

机构信息

Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials, Ministry of Education, School of Materials Science and Engineering, Shandong University, Jinan, 250061, P. R. China.

出版信息

Adv Sci (Weinh). 2023 Aug;10(23):e2300226. doi: 10.1002/advs.202300226. Epub 2023 Jun 6.

Abstract

Developing ionogel electrolytes based on ionic liquid instead of volatile liquid in gel polymer electrolytes is regarded to be effective to diminish safety concerns in terms of overheating and fire. Herein, a zwitterion-based copolymer matrix based on the copolymerization of trimethylolpropane ethoxylate triacrylate (ETPTA) and 2-methacryloyloxyethylphosphorylcholine (MPC, one typical zwitterion) is developed. It is shown that introducing zwitterions into ionogel electrolytes can effectively optimize local lithium-ion (Li ) coordination environment to improve Li transport kinetics. The interactions between Li and bis(trifluoromethanesulfonyl)imide (TFSI )/MPC lead to the formation of Li coordination shell jointly occupied by MPC and TFSI . Benefiting from the competitive Li attraction of TFSI and MPC, the energy barrier of Li desolvation is sharply decreased and thus the room-temperature ionic conductivity can reach a value of 4.4 × 10 S cm . Besides, the coulombic interaction between TFSI and MPC can greatly decrease the reduction stability of TFSI , boosting in situ derivation of LiF-enriched solid electrolyte interface  layer on lithium metal surface. As expected, the assembled Li||LiFePO cells deliver a high reversible discharge capacity of 139 mAh g at 0.5 C and good cycling stability. Besides, the pouch cells exhibit a steady open-circuit voltage and can operate normally under abuse testing (fold, cut), showing its outstanding safety performance.

摘要

在凝胶聚合物电解质中开发基于离子液体而非挥发性液体的离子凝胶电解质被认为是有效减少过热和火灾方面安全问题的方法。在此,基于三羟甲基丙烷乙氧基三丙烯酸酯(ETPTA)和2-甲基丙烯酰氧基乙基磷酰胆碱(MPC,一种典型的两性离子)的共聚反应,开发了一种基于两性离子的共聚物基质。结果表明,将两性离子引入离子凝胶电解质中可以有效地优化局部锂离子(Li⁺)配位环境,以改善Li⁺传输动力学。Li⁺与双(三氟甲磺酰)亚胺(TFSI⁻)/MPC之间的相互作用导致形成由MPC和TFSI⁻共同占据的Li⁺配位壳。受益于TFSI⁻和MPC对Li⁺的竞争性吸引,Li⁺去溶剂化的能垒急剧降低,因此室温离子电导率可达到4.4×10⁻³ S cm⁻¹。此外,TFSI⁻和MPC之间的库仑相互作用可以大大降低TFSI⁻的还原稳定性,促进在锂金属表面原位衍生富含LiF的固体电解质界面层。正如预期的那样,组装的Li||LiFePO₄电池在0.5 C下具有139 mAh g⁻¹的高可逆放电容量和良好的循环稳定性。此外,软包电池表现出稳定的开路电压,并且在滥用测试(折叠、切割)下能够正常运行,显示出其出色的安全性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc3/10427361/9e161ef72a4b/ADVS-10-2300226-g001.jpg

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