溶剂化
电解质
法拉第效率
锂(药物)
材料科学
金属锂
密度泛函理论
扩散
无机化学
电池(电)
化学工程
离子电导率
化学
金属
化学物理
电导率
枝晶(数学)
锂电池
离子液体
隐溶剂化
分解
分子动力学
电化学窗口
钾
锂离子电池
电化学
六氟磷酸盐
作者
Houhou Huang,Meihua Zhu,Zhiwei Wang,Ji Lv,Chuipeng Kong,Ming Feng,Fuquan Bai
出处
期刊:Energy & environmental materials
[Wiley]
日期:2026-01-02
被引量:1
摘要
Uncontrolled dendrite growth and low Coulombic efficiency remain major challenges limiting the practical application of rechargeable lithium metal batteries. Here, we introduce potassium hexafluorophosphate (KPF 6 ) as an additive to a commercial 1 m LiPF 6 ‐EC/DEC (1:1 vol%) electrolyte, which induces the formation of positively charged small aggregates in which a PF 6 − anion is shared between Li + and K + solvation structures. Molecular dynamics simulations reveal that the 0.1 m KPF 6 ‐containing electrolyte exhibits a higher Li + diffusion coefficient than in the baseline system, consistent with its enhanced ionic conductivity and transference numbers. Complementary density functional theory calculations show that these small aggregates possess lower solvation energies, facilitating Li + desolvation, while their reduced LUMO energy promotes LiPF 6 decomposition to generate a robust inorganic‐rich SEI. Experimentally, the KPF 6 additive drives the formation of a smooth, uniform, and ion‐conductive SEI on lithium metal, enabling Li‖LiFePO 4 cells to deliver superior rate capability and capacity retention. Pouch cell tests further underscore the practical potential of this electrolyte design. These findings highlight the role of small aggregates in solvation structure engineering and provide new insights for the development of high‐performance lithium metal batteries.
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