电解质
溶剂化
法拉第效率
相间
材料科学
化学物理
结合能
动力学
化学
化学工程
纳米技术
盐(化学)
静电学
储能
电池(电)
静电
电极
能量密度
强电解质
低能
离子
隐溶剂化
作者
Tianyang Xue,Zhengqiang Hu,Weilu Wang,Yi Chen,Xin Hu,Jin Yan,Fengling Zhang,Keqing Shi,Man Zhang,Li Li,Feng Wu,Ji Qian,Renjie Chen
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-11-14
卷期号:10 (12): 6157-6168
被引量:12
标识
DOI:10.1021/acsenergylett.5c02029
摘要
Lithium-metal batteries suffer from sluggish charge-transfer kinetics and unstable solid electrolyte interphase (SEI) layers under low temperatures, invariably leading to significant performance degradation. Herein, we propose a complementary “push and pull” electrolyte design strategy to controllably regulate the Li + solvation structure. The pull factor is designed to enhance the interaction between Li + and weakly solvating solvents, considering the electrostatic potential (ESP), Li + –solvent binding energy, solvent–solvent interactions, and F-donating ability. Furthermore, inorganic Li salt with a high Li + –anion binding energy is designed as a push factor to lower the Li + desolvation barrier and weaken the destructive effects of the pull factor on the SEI, forming a high-ionic-conductive and stable SEI. As a result, stable Li plating/stripping with high Coulombic efficiencies of 99.4% and 98.5% are achieved under −20 and −40 °C, respectively, and the Li/LiFePO 4 full cell can retain 73% of room-temperature capacity under −20 °C. These results demonstrate an effective electrolyte strategy for low-temperature Li-metal batteries.
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