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Surprising Relationship between Silicon Anode Calendar Aging and Electrolyte Components in a Localized High-Concentration Electrolyte System

  • Oak Ridge National Laboratory
  • University of Tennessee, Knoxville
  • Argonne National Laboratory

Research output: Contribution to journalArticlepeer-review

5 Scopus Citations

Abstract

Although localized high-concentration electrolytes (LHCEs) have been shown to improve the calendar lifetime of silicon anodes, the roles of the electrolyte constituents in calendar aging are not well understood. Here, we utilize a voltage hold protocol and an LHCE with varying molar ratios of lithium bis(fluorosulfonyl)imide (LiFSI), tetramethylene sulfone (TMS), and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTE) to probe the component roles during aging. Interestingly, the estimated calendar lifetime and irreversible lithium losses from the V-hold experiments are independent of the electrolyte formulations. Contrarily, the solid electrolyte interphase (SEI) composition depends on the electrolyte formulation. X-ray photoelectron spectroscopy shows that TMS-coordinated species decompose to form insoluble alkanes and lithium hydroxide (LiOH), while lithium fluoride (LiF) originates from the anion-coordination complex. The SEI composition does not appear to play a significant role in the silicon anode passivity, as measured by parasitic current, suggesting that the SEI-electrolyte interactions dictate the calendar aging mechanisms.
Original languageAmerican English
Pages (from-to)43020-43033
Number of pages14
JournalACS Applied Materials and Interfaces
Volume17
Issue number30
DOIs
StatePublished - 2025

NLR Publication Number

  • NREL/JA-5700-94538

Keywords

  • calendar aging
  • localized high concentration electrolyte
  • parasitic reactions
  • Si anode
  • solid electrolyte interphase

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