电解质
石墨
离子
化学
材料科学
化学工程
无机化学
有机化学
工程类
电极
物理化学
作者
Ling Che,Zhaowen Hu,Tao Zhang,Peiming Dai,Chengyu Chen,Chao Shen,Haitao Huang,Lifang Jiao,Ting Jin,Keyu Xie
标识
DOI:10.1002/bte2.20230064
摘要
Abstract 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 LiFePO 4 ||Gr pouch cell to exhibit 96.85% capacity retention at −20°C. Remarkably, LiFePO 4 ||Gr pouch cell with the designed electrolyte can still retain 66.28% of its room‐temperature capacity even at −40°C.
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