电解质
材料科学
电化学
电池(电)
离子电导率
储能
电极
电导率
钠
溶剂化
化学工程
离子键合
电化学电池
无机化学
电化学窗口
离子
相容性(地球化学)
磷酸三甲酯
纳米技术
电化学能量转换
快离子导体
离子液体
磷酸盐
丙酸盐
钠离子电池
半电池
电化学储能
作者
Xiangwu Chang,Jian Chen,Yang Liu,Siwei Fan,Chengye Lin,Wenjun Xu,Li Li,Xiao Ji,Minghong Wu,Yun Qiao
标识
DOI:10.1002/adfm.202515745
摘要
Abstract High‐safety sodium energy storage across a broad‐temperature range is essential for large‐scale energy storage systems. Effective ion transport in the electrolyte and stable interface phase on the electrode are essential prerequisites for the secure operation of sodium ion batteries under challenging environmental conditions. Herein, a non‐flammable electrolyte with high ionic conductivity is designed by incorporating low‐melting‐point, weak solvation methyl propionate (MP) and a flame‐retardant triethyl phosphate (TEP). The dipole‐dipole interaction between MP and TEP weakens the coordination of TEP, thereby increasing the proportion of anions involved in the solvation structure. This electrolyte configuration promotes the formation of a resilient inorganic‐enriched interface and enhances the electrode compatibility of the TEP‐based electrolyte, enabling the sodium vanadyl phosphate (NVP)||Na half cell and NVP||hard carbon (HC) full cell to deliver excellent electrochemical performance from −40 to 50 °C. Undoubtedly, this work proposes a new electrolyte design strategy based on synergistic dipole–dipole interaction, paving the way for high‐safety sodium‐ion batteries operating in extreme environments.
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