电解质
溶剂化
阳极
化学工程
金属
涂层
材料科学
溶剂
X射线光电子能谱
化学
无机化学
电极
有机化学
物理化学
纳米技术
工程类
作者
Guo‐Xing Li,Peter Lennartz,Volodymyr Koverga,Rong Kou,Au Nguyen,Heng Jiang,Meng Liao,Daiwei Wang,Naveen Dandu,Michael Zepeda,Haiying Wang,Ke Wang,Anh T. Ngo,Gunther Brunklaus,Donghai Wang
标识
DOI:10.1073/pnas.2311732121
摘要
Rechargeable lithium (Li) metal batteries face challenges in achieving stable cycling due to the instability of the solid electrolyte interphase (SEI). The Li-ion solvation structure and its desolvation process are crucial for the formation of a stable SEI on Li metal anodes and improving Li plating/stripping kinetics. This research introduces an interfacial desolvation coating technique to actively modulate the Li-ion solvation structure at the Li metal interface and regulate the participation of the electrolyte solvent in SEI formation. Through experimental investigations conducted using a carbonate electrolyte with limited compatibility to Li metal, the optimized desolvation coating layer, composed of 12-crown-4 ether-modified silica materials, selectively displaces strongly coordinating solvents while simultaneously enriching weakly coordinating fluorinated solvents at the Li metal/electrolyte interface. This selective desolvation and enrichment effect reduce solvent participation to SEI and thus facilitate the formation of a LiF-dominant SEI with greatly reduced organic species on the Li metal surface, as conclusively verified through various characterization techniques including XPS, quantitative NMR, operando NMR, cryo-TEM, EELS, and EDS. The interfacial desolvation coating technique enables excellent rate cycling stability (i.e., 1C) of the Li metal anode and prolonged cycling life of the Li||LiCoO 2 pouch cell in the conventional carbonate electrolyte (E/C 2.6 g/Ah), with 80% capacity retention after 333 cycles.
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