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Updated: Sep 8, 2025

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
Ion-Dipole Interactions Modulated Anion-Reinforced Solvation Chemistry for Advanced Wide-Temperature Sodium-Ion Full
Yun Wan1,2,3, Xiaoyan Shi1,2,3, Zhiming Zhou1,2,3
1Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, China.
None:
Wide-temperature sodium-ion batteries (SIBs) are considered promising candidates for large-scale energy storage systems under extreme temperature conditions. However, SIBs generally suffer from an unstable electrode-electrolyte interface (EEI) at high temperature and sluggish interfacial kinetics at low temperature, resulting in poor temperature tolerance with fast capacity degradation. Herein, a weakly coordinated carboxylate ester cosolvent, methyl butyrate, is employed to modulate the ion-dipole interactions in fluorine-free ester-based electrolyte for the anion-reinforced solvation chemistry. The unique solvent chemistry enables the construction of stable anion-derived inorganic-rich EEI on both cathode and anode surfaces while simultaneously reducing the desolvation energy barrier, thereby significantly enhancing the interfacial stability and kinetics. Therefore, the Prussian blue||hard carbon (PB||HC) full cell demonstrates a stable operation at a wide temperature range from -20 to 100 °C. Noticeably, the PB||HC 18650 cylindrical cell delivers a superior capacity retention of 91.41% after 230 cycles at an elevated temperature of 55 °C. This work provides valuable guidance for designing fluorine-free ester-based electrolytes through rational modulation of ion-dipole interactions, paving a promising pathway for wide-temperature sodium-ion full batteries.
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