Interconvertible and rejuvenated Lewis acidic electrolyte additive for lean electrolyte lithium sulfur batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 40707526.
- Also identified by DOI 10.1038/s41467-025-62169-z and PMC identifier 12289984.
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Abstract
Realizing practical lithium-sulfur batteries with high energy density requires lean electrolyte design. However, under low electrolyte/sulfur (E/S) ratios, highly concentrated lithium polysulfides in the electrolyte phase limit cycling and capacity. Here, we report that a small amount of Lewis acidic calcium cation in the electrolyte addresses the problems of lean electrolyte lithium-sulfur batteries. Because of its Lewis acidity, Ca<sup>2+</sup> readily converts lithium polysulfides into CaS and S<sub>8</sub>, preventing electrolyte jamming, polysulfide shuttle and Li corrosion. The in situ-formed CaS catalyzes the reduction reaction of lithium polysulfides. Ca<sup>2+</sup> rejuvenates via electrochemical oxidation of CaS during charging, enabling a sustainable interconversion between Ca<sup>2+</sup> and CaS during cycling. Li-S pouch cells with Ca<sup>2+</sup> additive delivered an energy density of 493 Wh kg<sup>-1</sup> (E/S of 2.4 μL mg<sup>-1</sup>) based on the total mass of the cell excluding external packaging, with 70% capacity retention at 220 cycle under 1 mA cm<sup>-2</sup> discharge, and 346 Wh kg<sup>-1</sup> (2.9 μL mg<sup>-1</sup>) with 77% capacity retention at 360 cycle under 1.0 C 2 mA cm<sup>-2</sup> discharge. The judicious integration of lithium-sulfur and calcium-sulfur chemistries offers a handy but effective approach to overcome the long-lasting trade-off between energy density and cycling stability in the development of lithium-sulfur batteries.