摘要
Low temperatures (< −20 °C) significantly diminish lithium-ion battery performance due to freezing issues within commercial electrolytes and the high energy barrier for Li+ desolvation at the interface. Although high-concentration electrolytes and localized high-concentration electrolytes enhance Li+ desolvation kinetics featuring anion-participated solvation structures, their high viscosity and propensity for Li salt precipitation render them unsuitable for low-temperature environments. This study introduces an anion-dominated conventional-concentrations electrolyte (ACCE) created by incorporating Lithium difluorophosphate(LiPO2F2)into a 1 M Lithium bis((trifluoromethyl)sulfonyl)azanide(LiTFSI) Dimethyl carbonate(DMC)/Fluoroethylene carbonate(FEC)/Methyl acetate(MA) electrolyte solution. LiPO2F2, characterized by its poor solubility and strong binding with Li+, demonstrates a pronounced tendency to integrate into the primary solvation sheath of Li+. Moreover, the synergy between LiTFSI and LiPO2F2 establishes a dual anion configuration, unveiling a dual anion-driven mechanism. This mechanism significantly diminishes the interaction between Li+ and solvent molecules, resulting in reduced desolvation energy under low temperatures. The ACCE exhibits high ionic conductivity of 1.3 mS cm−1 at −50 °C, enabling stable cycling of Li/NCM811 cells at −50 °C, and further allows 0.75 Ah graphite(Gr)/LiNi0.8Co0.1Mn0.1O2(NCM811) batteries dischargeable at −40 °C. This study presents a practical application potential for poorly soluble lithium salts and provides a new avenue for designing electrolytes suitable for low-temperature applications.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 2400337 |
| 期刊 | Advanced Functional Materials |
| 卷 | 34 |
| 期 | 33 |
| DOI | |
| 出版状态 | 已出版 - 14 8月 2024 |
| 已对外发布 | 是 |
联合国可持续发展目标
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学术指纹
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