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<p>The robust respective formations of a solid electrolyte interphase (SEI) and pillar at the surfaces of hard carbon and O3-type positive electrodes are the consequences of integrating LiPF<sub>6</sub> 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.</p><p></p>

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Transformative Effect of Li Salt for Proactively Mitigating Interfacial Side Reactions in Sodium-Ion Batteries

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年4月21日

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  • Jooeun Byun,
  • Joon Ha Chang,
  • Chihyun Hwang,
  • Chae Rim Lee,
  • Miseung Kim,
  • Jun Ho Song,
  • Boseong Heo,
  • Sunghun Choi,
  • Jong Hyeok Han,
  • Hee-Jae Jeon,
  • Beom Tak Na,
  • Youngjin Kim,
  • Ji-Sang Yu,
  • Hyun-seung Kim

摘要

The robust respective formations of a solid electrolyte interphase (SEI) and pillar at the surfaces of hard carbon and O3-type positive electrodes are the consequences of integrating LiPF6 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.