电解质
溶剂化
电化学
电池(电)
材料科学
化学工程
复合数
电导率
电极
电流密度
离子电导率
密度泛函理论
纳米技术
离子
无机化学
锂(药物)
离子键合
充电周期
电化学窗口
碳纳米管
超级电容器
容量损失
储能
相(物质)
扩散
作者
Enmin Li,Wei Shao,Huanming Wei,Xinlu Liu,Huanghao Pan,Bingqi Jiang,Chenjun Ju,Zhenglong Yang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-22
卷期号:20 (26): 18969-18983
被引量:1
标识
DOI:10.1021/acsnano.6c05928
摘要
Sodium-ion batteries have emerged as a promising alternative to lithium-ion batteries, offering distinct advantages that have garnered a significant amount of attention. However, challenges such as slow ion migration and unstable interfaces, stemming from the larger size and mass of sodium ions, severely impact the battery cycle life and fast-charging capabilities. To address these challenges, an effective solvation regulation strategy utilizing a trace amount of LiPF 6 additive is developed. The targeted introduction of LiPF 6 into the baseline NaPF 6 electrolyte induces the formation of unique Li + -Na + composite solvation structures, including “dual-anion” centered on Li + and ″Li + -Na + dual-cation″ with anions acting as bridges.This strategy not only enhances ionic conductivity and interfacial stability but also optimizes the structure of the Na 3 Fe 2 (PO 4 )P 2 O 7 (NFPP) electrode materials. Consequently, the capacity retention rate of NFPP∥Na batteries using this electrolyte surpassed 98% after 3000 cycles at 10 C, and the capacity retention rate of hard carbon (HC)∥Na batteries achieved 86.83% after 400 cycles at a current density of 1.0 A/g. Furthermore, when implemented in NFPP||HC pouch cells, the electrolyte maintained exceptional electrochemical performance even under charge and discharge cycles at a current density of 3 C. More importantly, this study extensively investigated the correlation between the constructed composite solvation structure and the electrochemical performance of the battery, providing a promising design approach for enhancing the performance of sodium-ion battery electrolytes in terms of both high-rate capability and extended cycle life.
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