Dense Li Deposition and Enhanced Flame-retardant Enabled by Localized Strong Ion-Dipole Interactions

被引:0
作者
Chen, Tao [1 ]
Sun, Lin [2 ]
Jin, Zhekai [2 ]
Liu, Yuncong [2 ]
Yan, Xinxiu [3 ]
Cui, Shuxun [1 ]
Wang, Chao [2 ]
机构
[1] Southwest Jiaotong Univ, Inst Smart City & Intelligent Transportat, Sch Chem, Chengdu 611756, Peoples R China
[2] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China
[3] Southwest Minzu Univ, Sch Chem & Environm, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
dense deposition; flame retardant; ion-dipole interactions; Li metal; solvation structure;
D O I
10.1002/chem.202500623
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Uncontrolled lithium (Li) deposition can lead to the formation of dendrites and "dead" Li, accelerating the degradation of cycling stability and safety performance in lithium metal batteries (LMBs). Herein, we propose a strategy to achieve dense Li deposition and flame-retardant by designing an electrolyte based on localized strong ion-dipole (LSID) interactions. The strong ion-dipole interactions between the multiple-dipole solvent (G4), NO3-, FSI-, and Li+ promote the formation of Li+ primary solvation sheaths for stabilizing Li deposition behavior. While the weak dipole fluorine-containing diluent (TTE) is distributed in the secondary solvation sheath due to weak ion-dipole interactions of Li+-TTE to improve interfacial wettability and flame retardancy due to preferential separation. Consequently, the localized strong ion-dipole interactions strategy in the designed electrolyte successfully achieves a Coulombic efficiency of more than 99% for Li||Cu cells, and ultrathin Li-matched Li||LFP and Li||NCM523 cells also demonstrate excellent cycling stability, as well as an improved safety performance of LMBs.
引用
收藏
页数:8
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