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salt into a sodium-ion battery electrolyte that considerably strengthens both interfaces of positive and negative electrodes. The improvement of cycle performances due to the formation of highly passivating SEI on the hard carbon electrode is induced by the alternated solvation structure following the addition of Li salt, which inhibits sodium-ion and electron leakage from further electrolyte decomposition. The SEI with incorporated Li is less soluble than Na-based SEI, and the passivation ability of the initially formed SEI can thus be well preserved. Conversely, the gas evolution caused by oxygen release is reduced considerably by the marginal surface intercalation of Li ions at the surface of the O3-positive electrode. Additionally, the LiF layer that forms on the O3 surface diminishes additional deterioration of the electrolyte after formation. Compared with the fluoroethylene carbonate additive that is typically applied, a simultaneously strengthened interface yields major improvements in capacity retention.
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Byun et al. (2025) studied this question.
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