钠
离子
金属
材料科学
化学工程
环境科学
化学
无机化学
冶金
工程类
有机化学
作者
Yiwen Gao,Haifeng Tu,Jiangyan Xue,Yan Wang,Shiqi Zhang,Suwan Lu,Lingwang Liu,Keyang Peng,Guochao Sun,Guangye Wu,Peng Ding,Yi Yang,Zhicheng Wang,Jingjing Xu,Xiaodong Wu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-06-19
卷期号:10 (7): 3315-3324
被引量:10
标识
DOI:10.1021/acsenergylett.5c01080
摘要
Rechargeable sodium ion batteries (SIBs) under extreme conditions are still limited by sluggish Na+ transport/desolvation kinetics and unstable electrode/electrolyte interface, thus leading to rapid capacity decay and a short lifespan. Herein, electrolyte engineering is proposed via solvent–solvent hydrogen bonding interaction between dimethyl sulfite (DMS) and glutaronitrile (GN) solvents for wide-temperature SIBs. The formed hydrogen bonding between DMS and GN solvents not only enhances the antioxidative ability of DMS but also simultaneously promotes the formation of a loose solvation structure by distancing DMS from Na+ ions, facilitating Na+ transport/desolvation kinetics. The well-designed electrolyte exhibits wide-temperature application from −55 to 60 °C in NaNi0.33Fe0.33Mn0.33O2 ||Na half cells, while the improved cycling stability with preactivated hard carbon anode is also obtained from −40 to 45 °C. This work sheds light on intersolvent synergistic effect for wide-temperature electrolyte design, specializing in regulating electrolyte thermodynamic and kinetic behavior.
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