材料科学
电解质
共晶体系
化学工程
纳米技术
电极
热稳定性
普鲁士蓝
储能
电池(电)
碳酸丙烯酯
相容性(地球化学)
硫化
吸附
分子
氢
热分解
作者
Jian Chen,Zhuo Yang,X. Hermione Xu,Yun Qiao,X. Hermione Xu,Xueting Liu,Yue Shen,Xinrun Yu,Xianluo Hu,Yang Liu,Zheng Liang,Yunhui Huang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-01-06
卷期号:11 (2): 1851-1860
被引量:2
标识
DOI:10.1021/acsenergylett.5c03502
摘要
Sodium-ion batteries are pivotal for energy storage due to their scalability and cost efficiency, although they face safety challenges arising from unstable interfaces, parasitic reactions, and thermal or mechanical stresses. Here, we present a universal electrolyte design strategy that incorporates elevated-dielectric-constant solvents, N -methylacetamide (NMA) and vinylene carbonate (VC), to optimize succinonitrile (SN)-based deep eutectic electrolytes. This approach enhances the compatibility of SN with Lewis bases while simultaneously improving the intrinsic safety at elevated temperatures. The robust hydrogen bonding network (C=O···H–C) between NMA and SN effectively immobilizes free SN molecules and reduces Na + coordination. Through competitive preferential adsorption at the electrode interface, NMA and VC exclude SN from the Helmholtz plane, thereby establishing an anion-rich interfacial phase that mitigates electrolyte consumption, dendrite growth, phase transitions, and gas evolution. As anticipated, Prussian blue||hard carbon pouch cells demonstrate enhanced flame-retardancy, improved shear resistance, and a capacity retention of 71.0% after 500 cycles.
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