Experimental study demonstrates high-capacity operation in a lithium-metal-free lithium-sulfur full cell, indicating a viable pathway toward safer commercial energy storage.
Progress in sulfur cathodes and separator interlayers has substantially curtailed polysulfide shuttling and sluggish kinetics in Li–S batteries. However, the instability of lithium metal anodes remains a major barrier to commercialization. Replacing lithium with mature lithiated graphite is attractive, but ether-based electrolytes used in Li–S cells induce Li + /solvent co‐intercalation and rapid failure of graphite electrodes. Building optimized interlayers and sulfur cathodes, this study focuses on making graphite fully compatible with ether electrolytes (DOL/DME). By systematically adjusting the lithium-salt concentration and LiNO 3 additive, we found a finely tuned compositional regime in which the graphite electrode is free from solvent co-intercalation without markedly impairing cathode kinetics. This enabled the integration of an H–TiO 2 /S cathode, a thin freestanding PVDF/MS interlayer, and a lithiated graphite anode into a full cell, which delivered 1066 mAh⋅g sulfur −1 at 0.1 C ( N/P = 0.87). The resulting prototype demonstrates that Li–S chemistry can operate without a lithium-metal anode, offering a practical route toward safer and more commercially viable Li–S batteries.
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Deng et al. (2026) studied this question.
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