电解质
材料科学
X射线光电子能谱
电导率
化学工程
离子电导率
羧酸盐
阴极
熔点
电化学
离子
扩散
化学
电极
有机化学
复合材料
物理化学
热力学
物理
工程类
作者
Yitong Liu,Hao‐Jie Liang,Miao Du,Jialin Yang,Zhen‐Yi Gu,Xiaotong Wang,Yuanzheng Tang,Jin‐Zhi Guo,Xing‐Long Wu
标识
DOI:10.1016/j.jmst.2023.09.040
摘要
With the continuous advancement of industrialization, sodium-ion batteries (SIBs) need to operate in various challenging circumstances, particularly in extremely cold conditions. However, at ultra-low temperatures, the reduced ionic conductivity and sluggish Na+ migration of commonly carbonate-based electrolytes will inevitably lead to a sharp decrease in the capacity of SIBs. Herein, we design a carboxylate ester-based electrolyte with excellent ultra-low temperature performance by straightforward cosolvent strategy. Due to the low viscosity, melting point, and sufficient ionic conductivity of the designed electrolyte, the resulting Na||Na3V2(PO4)2O2F can achieve the capacity retention of 96% (100 cycles at 0.1 C) at –40 °C and can also operate stably even at –50 °C. Besides, galvanostatic intermittent titration technique (GITT), ex-situ X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (TEM) tests are employed to analyze and confirm that the carboxylate ester-based electrolyte promotes robust and uniform cathode/electrolyte interface layer formation and accelerates ion diffusion kinetics, which collectively facilitates the better low-temperature performance. In addition, the assembled hard carbon||NVPOF full cells further prove the practicability of the carboxylate ester-based electrolyte at low-temperature, which delivers high discharge capacity of 108.4 and 73.0 mAh g–1 at –25 and –40 °C. This work affords a new avenue for designing advanced low-temperature electrolytes for SIBs.
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