阴极
电化学
材料科学
硫酸盐
氧化还原
电池(电)
化学工程
硫酸钾
无机化学
离子半径
扩散
钾离子电池
离子键合
硫酸钠
电解质
钾
容量损失
吸收(声学)
晶体结构
衍射
钠离子电池
分析化学(期刊)
电极
吸收光谱法
离子
化学
钠
离子交换
结构稳定性
Crystal(编程语言)
作者
Xinyue Xu,Guodong Li,Hao Zhang,Nan Wang,Tinghang Xu,Hui Yang,Jie Xu,Baofeng Wang,Junxi Zhang,Zhaolu Liu,Yongjie Cao
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-09-30
卷期号:18 (11): 94908121-94908121
被引量:2
标识
DOI:10.26599/nr.2025.94908121
摘要
Iron-based sulfates have emerged as promising cathode materials for potassium-ion batteries due to its low cost, high working potential, and environmentally friendly. However, the relatively large ionic radius and sluggish diffusion coefficient of K-ion pose significant challenges to the electrochemical performance and structural stability of cathode materials in PIBs. In this work, we successfully synthesis a new iron-based sulfate cathode material, potassium sodium iron sulfate (K1.66Na1.02Fe1.66(SO4)3, KNFS), through an electrochemical ion exchange method. As a cathode material, it exhibits a reversible specific capacity of 83 mAh g-1 and an average working potential of 3.84 V (vs. K/K+) at 0.1 C in PIBs. Even at 2 C, it still demonstrates a reversible specific capacity of 52 mAh g-1 with a capacity retention ratio of 88.2 % after 300 cycles. The in-situ X-ray diffraction (XRD) and ex-situ X-ray absorption spectroscopy reveal that the K-ion storage mechanism in KNFS is predominantly governed by the reversible Fe3+/Fe2+ redox couple, which provides a theoretical specific capacity of 94 mAh g-1 and involves minimal volume change (2.57 %). The first-principles calculations combined with XRD results indicate that the KNFS cathode exhibits a typical alluaudite-type crystal structure with multiple fast K-ion migration channels along the three-dimensional orientation.
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