电解质
电池(电)
钠
溶剂
离子
化学
无机化学
化学工程
材料科学
有机化学
工程类
热力学
物理
物理化学
电极
功率(物理)
作者
Soohwan Kim,Vinay Mirzapure,Rasha Atwi,Heramba V. S. R. M. Koppisetti,Kundan Wasnik,Nav Nidhi Rajput,Manjusha V. Shelke,Vilas G. Pol
出处
期刊:PubMed
日期:2025-07-24
卷期号:: e02142-e02142
标识
DOI:10.1002/smtd.202402142
摘要
Sodium-ion batteries (SIBs) show promise as an alternative to lithium-ion batteries. However, they face performance challenges at ultra-low temperatures (<-40 °C) due to slow Na+ transfer kinetics with conventional electrolytes. This limitation restricts their use in extreme environments such as polar regions and outer space. The presented systematic study addresses this challenge by modulating and tailoring the electrolyte composition for SIBs, enabling ultra-low temperature operation down to -110 °C for the first time. The comprehensive molecular dynamic and density functional theory calculations combined with experimental Raman spectroscopy and nuclear magnetic resonance studies of advanced electrolytes provided a deeper mechanistic understanding of the solvation structures and their impact on electrochemical performance. By varying the solvent composition with a combination of tetrahydrofuran and 2-Methyltetrahydrofuran solvents and sodium hexafluorophosphate (NaPF6) salt, the freezing point, solubility, and Na+ solvation structure of the electrolyte is modulated and studied in detail. The extensive anion engagement in the optimized mix solvent electrolyte facilitated the formation of a stable and inorganic-rich solid electrolyte interphase layer, ensuring low overpotentials and uniform Na+ deposition, yielding superior cycling stability. As a result, the developed electrolyte enables SIBs to achieve reversible capacities of 88 mAh g-1 at -60 °C and 50 mAh g-1 at -100 °C. These insights may contribute to developing improved energy storage devices suitable for challenging environmental conditions.
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