Related Experiment Video
Updated: May 15, 2025

Three-electrode Coin Cell Preparation and Electrodeposition Analytics for Lithium-ion Batteries
Published on: May 22, 2018
Dense Li Deposition and Enhanced Flame-retardant Enabled by Localized Strong Ion-Dipole Interactions
Tao Chen1, Lin Sun2, Zhekai Jin2
1Institute of Smart City and Intelligent Transportation, School of Chemistry, Southwest Jiaotong University, Chengdu, 611756, P. R. China.
Abstract:
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.
Related Concept Videos
Ionic Bonding and Electron Transfer
Trends in Lattice Energy: Ion Size and Charge
Bond Polarity, Dipole Moment, and Percent Ionic Character
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Molecular Shape and Polarity
Intermolecular Forces

