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用于快速充电高压锂金属电池的配位调控使能型深共晶电解质

Coordination Regulation Enabling Deep Eutectic Electrolyte for Fast-Charging High-Voltage Lithium Metal Batteries.

作者信息

Ding Peipei, Yuan Haocheng, Xu Ligang, Wu Lingqiao, Du Haozhe, Zhao Shu, Yu Dengfeng, Qin Zuoyu, Liu Hong, Li Yue, Zhang Xu, Yu Haijun, Tang Mingxue, Ren Yaoyu, Li Liangliang, Nan Ce-Wen

机构信息

State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084, China.

Center for High Pressure Science & Technology Advanced Research, Beijing, 100193, China.

出版信息

Adv Mater. 2025 Feb;37(6):e2413654. doi: 10.1002/adma.202413654. Epub 2024 Dec 19.

Abstract

The safety and cycle stability of lithium metal batteries (LMBs) under conditions of high cut-off voltage and fast charging put forward higher requirements for electrolytes. Here, a sulfonate-based deep eutectic electrolyte (DEE) resulting from the eutectic effect between solid sultone and lithium bis(trifluoromethanesulfonyl)imide without any other additives is reported. The intermolecular coordination effect triggers this eutectic phenomenon, as evidenced with nuclear magnetic resonance, and thus the electrochemical behavior of the DEE can be controlled by jointly regulating the coordination effects of F···H and Li···O intermolecular interactions. The DEE with a properly coordinated environment of Li presents a low motion barrier and a high transport rate of localized Li, leading to a 10 C fast-charging LiFePO||Li battery with a capacity retention of 95.1% after 500 cycles. Meanwhile, the strengthened α-H···F coordination broadens the electrochemical stability window of the DEE, thus enabling the cycle stability of high-capacity and high-voltage cathode materials in LMBs, e.g., a cycle stability at 4.5 V in the LiNiCoMnO||Li battery with a capacity retention of 81.0% after 500 cycles, and an excellent compatibility in 4.5 V LiCoO||Li and 4.8 V LiMnNiCoO||Li batteries. The practical applicability of the carefully designed DEE is underscored through successful implementation in pouch cells.

摘要

锂金属电池(LMBs)在高截止电压和快速充电条件下的安全性和循环稳定性对电解质提出了更高要求。在此,报道了一种基于磺酸盐的深共晶电解质(DEE),它由固体磺内酯与双(三氟甲烷磺酰)亚胺锂之间的共晶效应产生,无需任何其他添加剂。分子间配位效应引发了这种共晶现象,核磁共振证实了这一点,因此DEE的电化学行为可以通过共同调节F···H和Li···O分子间相互作用的配位效应来控制。具有适当Li配位环境的DEE呈现出低迁移势垒和局部Li的高传输速率,从而实现了10 C快速充电的LiFePO||Li电池,在500次循环后容量保持率为95.1%。同时,增强的α-H···F配位拓宽了DEE的电化学稳定窗口,从而实现了LMBs中高容量和高电压正极材料的循环稳定性,例如,在LiNiCoMnO||Li电池中4.5 V下的循环稳定性,500次循环后容量保持率为81.0%,并且在4.5 V LiCoO||Li和4.8 V LiMnNiCoO||Li电池中具有优异的兼容性。精心设计的DEE通过在软包电池中的成功应用突出了其实际适用性。

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