氟化锂
氟化物
电解质
氟化钾
锂(药物)
无机化学
材料科学
法拉第效率
磺酰
X射线光电子能谱
电池(电)
化学工程
锰
有机硫化合物
锂硫电池
阴极
化学
锂离子电池
锂电池
作者
Myeong Ju Lee,Sun Bu Lee,Byeong Jun Koo,Yura Kim,Jinseo Kim,Chanyoung Lee,노은빈,Jonghoon Kim,Han Yong Bae,Jimin Oh
出处
期刊:Small
[Wiley]
日期:2026-07-15
卷期号:22 (49): e74510-e74510
摘要
ABSTRACT High‐nickel lithium nickel cobalt manganese oxide (NCM) cathodes suffer interfacial instability that impairs initial efficiency and long‐term cycling. To overcome those problems, we evaluate a series of five sulfonyl fluoride (–SO 2 F) electrolyte additives—Ethenesulfonyl fluoride (A), 2‐(Benzylthio)‐2‐phenylethane‐1‐sulfonyl fluoride (B), 2‐Chloroethane‐1‐sulfonyl fluoride (C), Methyl 2‐(fluorosulfonyl)acetate (D), Methanesulfonyl fluoride (E) for high‐nickel NCM cells. Additives C and E yielded the highest initial Coulombic efficiencies (ICE) (∼90%), markedly higher than other additives. Additives B and E showed higher specific discharge capacity (∼230 mAh/g). X‐ray photoelectron spectroscopy (XPS) revealed that the effective additives E form F‐rich and S‐containing interfacial layers (e.g., LiF and organosulfur species), in contrast to a negligible S signal without additives. These findings demonstrate that –SO 2 F functional additives can significantly enhance the initial efficiency and interphase stability of Ni‐rich cathodes. The results correlate the molecular structure of additives to their film‐forming behavior: proper small alkyl–SO 2 F (E) effectively form protective interphases. This study qualitatively evaluated the influence of SO 2 F moieties on high‐energy lithium battery performance depending on the surrounding materials and provides material‐function‐performance insights for the design of functional electrolyte additives to enhance battery performance.
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