Kim Soohwan, Mirzapure Vinay, Atwi Rasha, Koppisetti Heramba V S R M, Wasnik Kundan, Rajput Nav Nidhi, Shelke Manjusha, Pol Vilas G
Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, 47907, USA.
Physical and Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune, Maharashtra, 411008, India.
Small Methods. 2025 Sep;9(9):e02142. doi: 10.1002/smtd.202402142. Epub 2025 Jul 24.
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 (NaPF) 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 around 81 mAh g at -60 °C and around 21 mAh g at -100 °C. These insights may contribute to developing improved energy storage devices suitable for challenging environmental conditions.
钠离子电池(SIBs)有望成为锂离子电池的替代品。然而,由于传统电解质中钠离子转移动力学缓慢,它们在超低温(<-40°C)下面临性能挑战。这一限制阻碍了它们在极地地区和外层空间等极端环境中的应用。本文提出的系统研究通过调节和定制钠离子电池的电解质成分来应对这一挑战,首次实现了低至-110°C的超低温运行。先进电解质的综合分子动力学和密度泛函理论计算,结合拉曼光谱和核磁共振实验研究,为溶剂化结构及其对电化学性能的影响提供了更深入的机理理解。通过将四氢呋喃和2-甲基四氢呋喃溶剂与六氟磷酸钠(NaPF)盐混合来改变溶剂组成,对电解质的冰点、溶解度和钠溶剂化结构进行了调节和详细研究。优化混合溶剂电解质中广泛的阴离子相互作用促进了稳定且富含无机物的固体电解质界面层的形成,确保了低过电位和均匀的钠沉积,产生了优异的循环稳定性。结果,所开发的电解质使钠离子电池在-60°C时能够实现约81 mAh g的可逆容量,在-100°C时能够实现约21 mAh g的可逆容量。这些见解可能有助于开发适用于具有挑战性环境条件的改进型储能装置。