4.8 Article

Establishing the Preferential Adsorption of Anion-Dominated Solvation Structures in the Electrolytes for High-Energy-Density Lithium Metal Batteries

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 30, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202011109

Keywords

anion-dominated solvation structures; electrolytes; lithium metal batteries; preferential adsorption

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. University of Waterloo
  3. Waterloo Institute for Nanotechnology
  4. Outstanding Youth Project of Guangdong Natural Science Foundation [2021B1515020051]
  5. Department of Science and Technology of Guangdong province [2019JC01L203, 2020B0909030004]
  6. Science and Technology Program of Guangzhou [2019050001]
  7. Yunnan Expert Workstation [202005AF150028]

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This study reveals that the unstable solid electrolyte interface (SEI) in Li metal batteries (LMBs) mainly originates from the kinetic instability of Li+-solvation structures in the electrolyte. By integrating preferentially adsorbed anions into the Li+-solvation structures, the formation of an anion-derived SEI layer with high Li-ion conductivity and low Li atom adhesion energy is achieved, facilitating high Coulombic efficiency and stable cycling in realistic testing conditions.
The practical application of Li metal batteries (LMBs) is severely hindered by the unstable solid electrolyte interface (SEI). In this work, it is revealed that the unstable SEI mainly originates from the kinetic instability of Li+-solvation structures in the electrolyte which can result in continuous electrolyte decomposition and nonuniform Li deposition. To address this issue, preferential adsorption of anion-dominated solvation complexes (A-Coms) are established by integrating preferentially adsorbed anions (NO3- and Li2S8) into the Li+-solvation structures. In these structures, the locations of the lowest unoccupied molecular orbital energy level shift from solvents to anions, rendering a relieved electrolyte decomposition and an anion-derived SEI formation. Meanwhile, the anions in the A-coms preferentially adsorb on the Li metal surfaces due to their stronger chemisorption capability toward lithium metal anodes (LMAs) compared to the solvent molecules, effectively shielding solvent molecules from parasitic reaction with LMAs. Furthermore, the anion-derived SEI exhibits high Li-ion conductivity and low Li atom adhesion energy, which can facilitate uniform Li deposition. Consequently, this electrolyte can enable a high Li plating/stripping Coulombic efficiency of 98.5% over 500 cycles and a stable cycling under realistic testing conditions with a high-energy-density of 310 W h kg(-1) based on a full cell configuration.

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