电解质
过电位
溶剂化
阳极
石墨
相间
化学工程
插层(化学)
离子电导率
电导率
材料科学
工作(物理)
电荷(物理)
化学物理
电化学
离子
化学
无机化学
电极
物理化学
有机化学
热力学
复合材料
物理
生物
工程类
遗传学
量子力学
作者
Yang Yang,Fang Zhong,Yue Yin,Yongjie Cao,Yonggang Wang,Xiaoli Dong,Yongyao Xia
标识
DOI:10.1002/anie.202208345
摘要
Abstract Graphite anode suffers from great capacity loss and even fails to charge ( i.e . Li + ‐intercalation) under low temperature, mainly arising from the large overpotential including sluggish de‐solvation process and insufficient ions movement in the solid electrolyte interphase (SEI). Herein, an electrolyte is developed by utilizing weakly solvated molecule ethyl trifluoroacetate and film‐forming fluoroethylene carbonate to achieve smooth de‐solvation and high ionic conductivity at low temperature. Evolution of SEI formed at different temperatures is further investigated to propose an effective room‐temperature SEI formation strategy for low‐temperature operations. The synergetic effect of tamed electrolyte and optimized SEI enables graphite with a reversible charge/discharge capacity of 183 mAh g −1 at −30 °C and fast‐charging up to 6C‐rate at room temperature. Moreover, graphite||LiFePO 4 full cell maintains a capacity retention of 78 % at −30 °C, and 37 % even at a super‐low temperature of −60 °C. This work offers a progressive insight towards fast‐charging and low‐temperature batteries.
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