4.8 Article

Superior long-term cycling of high-voltage lithium-ion batteries enabled by single-solvent electrolyte

Journal

NANO ENERGY
Volume 89, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2021.106299

Keywords

High-voltage lithium-ion batteries; High-voltage electrolyte; Single-solvent electrolyte; Solid-electrolyte interphase; Aluminum corrosion

Funding

  1. U.S. Department of Energy (DOE)
  2. Vehicle Technologies Office (VTO)
  3. DOE Office of Science by UChicago Argonne, LLC [DE-AC02-06CH11357]
  4. Applied Battery Research for Transportation Program
  5. University of California
  6. National Science Foundation Major Research Instrumentation Program [CHE-1338173]

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A new single-solvent electrolyte system with lithium bis(fluorosulfonyl) imide (LiFSI) and beta-fluorinated sulfone (TFPMS) was designed to enable stable cycling of high-voltage lithium-ion batteries. The system displayed outstanding compatibility with graphite and improved cycling performance, making it a promising solution for high-voltage battery applications.
A new single-solvent electrolyte system comprising lithium bis(fluorosuflonyl) imide (LiFSI) and beta-fluorinated sulfone (TFPMS) was designed to enable very stable long-term cycling of high-voltage lithium-ion batteries. Compared to other fluorinated solvents such as alpha-fluorinated sulfone (FMES) and fluorinated carbonate (FEMC), which are prone to reduction on the graphite anode, the LiFSI-TFPMS system displayed outstanding compatibility with graphite. While regular carbonate and sulfone from the LiFSI electrolyte system are compatible with the graphite anode, their high solvating power not only induces severe corrosion on the aluminum cathode current collector at high voltage, but also renders a low aggregation level at a normal salt concentration (about 1.0 M), resulting in the formation of an unstable solid-electrolyte interphase (SEI) on the graphite anode. Owing to the low solvating power of TFPMS, the aggregation level of the LiFSI-TFPMS system is relatively high even at normal salt concentration, which not only facilitates the formation of a robust SEI by the sacrificial decomposition of LiFSI, but also suppresses the aluminum corrosion of the LiFSI electrolyte system at high voltage. Together with the high intrinsic anodic stability of TFPMS, the superior cycling performance of graphite parallel to LiNi0.6Co0.2Mn0.2O2 cells was achieved by employing the non-flammable LiFSI-TFPMS single-solvent electrolyte system.

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