Interfacial solvation-structure regulation for stable Li metal anode by a desolvation coating technique

Author:

Li Guo-Xing1ORCID,Lennartz Peter2ORCID,Koverga Volodymyr34,Kou Rong1,Nguyen Au5,Jiang Heng1,Liao Meng1ORCID,Wang Daiwei1,Dandu Naveen34,Zepeda Michael3ORCID,Wang Haiying6,Wang Ke6,Ngo Anh T.34,Brunklaus Gunther2ORCID,Wang Donghai1ORCID

Affiliation:

1. Department of Mechanical Engineering, The Pennsylvania State University, University Park, PA 16802

2. Forschungszentrum Jülich, Helmholtz Institute Münster, Münster 48149, Germany

3. Department of Chemical Engineering, University of Illinois Chicago, Chicago, IL 60608

4. Materials Science Division, Argonne National Laboratory, Lemont, IL 60439

5. Department of Materials Science and Engineering, The Pennsylvania State University, University Park, PA 16802

6. Materials Research Institute, The Pennsylvania State University, University Park, PA 16802

Abstract

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.

Funder

DOE-Argonne National Lab

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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