The concept of employing highly concentrated electrolytes has been widely incorporated into electrolyte design, due to their enhanced Li-metal passivation and oxidative stability compared to their diluted counterparts. However, issues such as high viscosity and sub-optimal wettability, compromise their suitability for commercialization. In this study, we present a highly concentrated dimethyl ether-based electrolyte that appears as a liquid phase at ambient conditions via Li+ - solvents ion-dipole interactions (Coulombic condensation). Unlike conventional high salt concentration ether-based electrolytes, it demonstrates enhanced transport properties and fluidity. The anion-rich solvation structure also contributes to the formation of a LiF-rich salt-derived solid electrolyte interphase, facilitating stable Li metal cycling for over 1000 cycles at 0.5 mA cm-2, 1 mAh cm-2 condition. When combined with a sulfurized polyacrylonitrile (SPAN) electrode, the electrolyte effectively reduces the polysulfide shuttling effect and ensures stable performance across a range of charging currents, up to 6 mA cm-2. This research underscores a promising strategy for developing an anion-rich, high concentration ether electrolyte with decreased viscosity, which supports a Li metal anode with exceptional temperature durability and rapid charging capabilities.
Keywords: Electrolyte; Fast Charge; Ion-dipole interaction; Li/Sulfur Batteries; Solvation structure.
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