Abstract
To date, it is extensively believed that ether electrolytes are incompatible with graphite anode in Li-ion batteries due to detrimental solvent co-intercalation and exfoliation. Here, we provide design criteria of ether electrolytes for reversible graphite anode without the high salt concentration. In short, for ether electrolytes, the reductive stability of anions (or their solvated complex) and the solid-electrolyte interphase (SEI) govern the reversibility of graphite anode. Exfoliation and co-intercalation are not the root cause of as-documented cell failures using graphite anodes. While reductive-instable lithium bis(fluorosulfonyl)imide (LiFSI) is the optimal salt paired with DOL, reductive-stable LiBF4 finds applications with DME. Individual 1,3-dioxolane (DOL) and 1,2-dimethoxyethane (DME) based electrolytes can enable ~99.9% Coulombic efficiency with excellent capacity retention and fast-charge capability using natural graphite. In DOL electrolytes, weakened Li-solvent interaction and preferential reduction of FSI anion coordinated with Li-ion contribute to homogeneous SEI enriched with inorganic species, for example, LiF. Therefore, electrolyte reduction and Li-DOL co-intercalation are inhibited. In DME electrolytes, we show that LiBF4 has limited reduction, majorly on the edge site. We discover that a self-terminating, heterogeneous interphase based on grainy LiF proves to be desirable for operating Li-solvent co-intercalation. Taking advantage of the anisotropic characteristics of natural graphite, we conducted a holistic investigation into the nature, function, and formation of the heterogeneous SEI. In these studies, we clarify a long-lasting confusing issue in LIBs community-that is, the compatibility between ether electrolytes and graphite anode. Our findings not only shed light on the enigmatic interphase formed by ether electrolytes but also offer critical insights into future electrolyte design for graphite anodes operated under extreme conditions.
Published Version
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