Neighboring alkenyl group participated ether-based electrolyte for wide-temperature lithium metal batteries

邻位烯基参与了宽温锂金属电池的醚基电解质的制备

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Abstract

The extensive dendrite formation and unstable interfacial chemical environment pose significant obstacles to operating lithium metal batteries under extreme conditions. Here, we develop an allyl ether electrolyte operated across a wide-temperature range. Leveraging the neighboring group participation effect of alkenyl groups, the designed electrolyte possesses a quasi-weak solvation structure with low desolvation energy. Moreover, this effect facilitates the anion decomposition to form a dual-layer solid electrolyte interface, suppressing dendrite formation and surface parasitic reactions. Therefore, the single-salt, single-solvent electrolyte enables reversible lithium plating/stripping with high Coulombic efficiencies from -40 °C to 60 °C. The assembled 50 μm lithium | |3.5 mAh cm(-2) sulfurized polyacrylonitrile full cells achieve capacity retention of 93.1% after 150 stable cycles (0.2 C) at 25 °C, where the positive electrode could retain 78% of its room temperature capacity at -40 °C. Moreover, the pouch cells demonstrate promising cycling stabilities, with a capacity retention of 94.8% (0.5 C), 92.4% (0.2 C), and 72.7% (0.1 C) after 100 cycles at 60 °C, 25 °C, and -40 °C, respectively. This terminal group modification strategy offers perspectives for wide-temperature electrolyte design, representing a crucial advancement in enhancing the performance of lithium metal batteries.

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