摘要
Lithium-ion batteries suffer from severe capacity loss and even fail to work under subzero temperatures, which is mainly due to the sluggish Li+ transportation in the solid electrolyte interphase (SEI) and desolvation process. Ethyl acetate (EA) is a highly promising solvent for low-temperature electrolytes, yet it has poor compatibility with graphite (Gr) anode. Here, we tuned the interfacial chemistry of EA-based electrolytes via synergies of anions. ODFB− with low solvation numbers, participates in the solvation sheath, significantly reducing the desolvation energy. Meanwhile, combined with the high dissociation of FSI−, the reduction of both anions constructs an inorganic-rich SEI to improve interfacial stability. The electrolyte enables Gr anode to deliver a capacity of 293 mA h g−1 and 2.5 Ah LiFePO4||Gr pouch cell to exhibit 96.85% capacity retention at −20°C. Remarkably, LiFePO4||Gr pouch cell with the designed electrolyte can still retain 66.28% of its room-temperature capacity even at −40°C.
源语言 | 英语 |
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文章编号 | 20230064 |
期刊 | Battery Energy |
卷 | 3 |
期 | 3 |
DOI | |
出版状态 | 已出版 - 5月 2024 |