电解质
阳极
离子电导率
材料科学
溶解
化学工程
电导率
聚合物
电化学
聚合物电解质
离子键合
航程(航空)
大气温度范围
电化学电池
耐久性
离子液体
无机化学
纳米技术
电极
作者
Jiaxuan Wang,Chunye Yang,Jing Wang,Xinping Ai,Yuliang Cao,Yongjin Fang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-03-11
卷期号:11 (4): 3386-3394
被引量:1
标识
DOI:10.1021/acsenergylett.6c00051
摘要
Solid polymer electrolytes are pivotal to safe, high-energy sodium–metal batteries but suffer from low ionic conductivity and poor interfacial stability. Here we pioneer a single-salt quasi-solid polymer electrolyte (PSDF) using NaDFOB, where dissolution is driven by interaction with C–O–C bonds rather than C═O groups. Together with succinonitrile-optimized solvation, PSDF achieves an ionic conductivity of 0.89 mS cm–1, a Na+ transference number of 0.58, and an oxidation potential of 5.1 V (vs Na+/Na). DFOB– preferentially forms B/F-rich interphases on both anode and cathode, enabling good interfacial stability. This allows the Na||PSDF||Na3V2(PO4)3 cell to retain 98.2% capacity after 3500 cycles, while operating effectively across a wide temperature range (−10 to 90 °C). Impressively, the cell respectively maintains 98 and 81.2% of its room-temperature capacity at 0 and −10 °C, and retains capacity retention >85% after 500 cycles at 80 and 90 °C. Besides, the Na||PSDF||Na3V2(PO4)3 pouch cells also show decent electrochemical performance and safety.
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