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 language | American English |
|---|---|
| Pages (from-to) | 43020-43033 |
| Number of pages | 14 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 17 |
| Issue number | 30 |
| DOIs | |
| State | Published - 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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