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Research Article | Open Access

Separated Solvated Ion Pair-Assisted Aqueous Electrolyte for Supercapacitor at Ultralow Temperature

Dewei Xiao1Zhemin Li1Lanxin Yan1Jiayin Shi1Jianwei Xiong1Zhenming Xu1Xiaoli Dong2 ( )Xiaogang Zhang1 ( )
Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies, College of Material Science and Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai 200433, China
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Abstract

Aqueous electrolytes have the advantages of low cost, environmental friendliness, and fast ion transport kinetics, which show great low-temperature potential. However, the high freezing point limit practical applications. In electrolytes, the design of ion pairs can effectively improve the charge transport properties, while its effect on low-temperature performance is neglected. Here, we acquired the lithium trifluoromethanesulfonate (LiOTf)-based aqueous electrolytes with different ion pair structures. Using advanced characterization and simulation, it was revealed that the 10 m LiOTf electrolyte-enriched separated solvated ion pairs (SSIPs) show excellent ultralow-temperature stability. The changes in energy storage behavior under different temperature were discussed, which revealed that SSIPs contribute to efficient adsorption at low temperatures. The supercapacitor with 10 m LiOTf reached high energy density of 34.67 Wh/kg at −40 ℃ and maintained long cycle stability at −70 ℃. Our work suggests a strategy for the rational design of electrolytes that could enable next-generation ultralow-temperature electrochemical storage systems.

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Energy Material Advances
Article number: 0189

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Cite this article:
Xiao D, Li Z, Yan L, et al. Separated Solvated Ion Pair-Assisted Aqueous Electrolyte for Supercapacitor at Ultralow Temperature. Energy Material Advances, 2026, 7: 0189. https://doi.org/10.34133/energymatadv.0189

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Received: 22 October 2024
Revised: 03 January 2025
Accepted: 03 February 2025
Published: 16 January 2026
© 2026 Dewei Xiao et al. Exclusive licensee Beijing Institute of Technology Press. No claim to original U.S. Government Works.

Distributed under a Creative Commons Attribution License (CC BY 4.0).