电解质
溶剂化
相间
阳极
钠
离子
电池(电)
化学工程
电化学窗口
电化学
电池电压
熵(时间箭头)
储能
化学
材料科学
能量密度
电压
纳米技术
充电周期
溶剂
电极
无机化学
电化学电池
离子电导率
容量损失
碳纤维
作者
Wensha Niu,Peng-Tao Guo,Ming‐Yuan Shen,Tao Wu,Bin He,Haoquan Hu,Hongliang Xie,Jun Ming,Wen‐Cui Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-10-20
卷期号:10 (11): 5542-5549
被引量:8
标识
DOI:10.1021/acsenergylett.5c02840
摘要
Designing electrolytes compatible with hard carbon (HC) anodes that withstand a wider voltage window remains a challenge in sodium-ion batteries. Herein, we develop high-entropy electrolytes by taking a propylene carbonate-based electrolyte as a paradigm, in which various solvents were deliberately introduced to tune the entropy of the electrolyte solvation structure. The formulated high-entropy electrolytes can withstand a voltage of 4.35 V, enabling the Na 0.75 Li 0.15 Mg 0.05 Ni 0.1 Mn 0.7 O 2 ||HC full cell to deliver a specific capacity of 114.8 mAh g –1 and to exhibit enhanced rate capabilities and cycling performance. In particular, the cell achieves an energy density of 361.1 Wh kg cathode –1 while preserving a capacity retention of 89.2% after 500 cycles without any presodiation treatment. We not only evaluated the individual roles of each electrolyte component to validate the strategy but also characterized the evolution of the electrolyte-electrode interphase in different electrolytes to elucidate the improved battery performance.
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