阴极
扫描电子显微镜
钾
电化学
材料科学
锰
微观结构
兴奋剂
过渡金属
离子
分析化学(期刊)
化学工程
电极
复合材料
冶金
化学
物理化学
光电子学
色谱法
有机化学
催化作用
工程类
作者
Cai‐ling Liu,Shaohua Luo,Hongbo Huang,Xin Liu,Zhai Yu-chun,Zhaowen Wang
标识
DOI:10.1016/j.cej.2019.122167
摘要
Abstract A series of iron-substituted layered P3-type manganese oxides, K0.45Mn1−xFexO2 (x = 0, 0.1, 0.2, 0.3, 0.4 and 0.5) were fabricated using a convenient solid-state method and studied as cathode materials for potassium-ion batteries. The microstructure and morphology of the as-synthesized materials were examined by X-ray diffraction (XRD) and scanning electron microscope (SEM) techniques. The electrochemical characteristics of K0.45Mn1−xFexO2 samples have been investigated systematically and K0.45Mn0.8Fe0.2O2 shows the best cyclic stability and highest rate performance. It delivers a large reversible discharge capacity of 106.2 mAh g−1 at 20 mA g−1 with a capacity retention rate of 77.3% after 100 cycles. It also presents obviously enhanced rate performance with the capacity of 64.9 mAh g−1 at 200 mA g−1 and stable cycling capability of 44.7 mAh g−1 after 100 cycles. The results demonstrate that the relatively small substitution (20%) at the transition metal site can improve the cycle stability during potassium ions insertion and extraction. Therefore, the layered P3-K0.45Mn0.8Fe0.2O2 possibly serves as a potentially promising cathode material that made from completely earth-abundant elements for potassium-ion batteries applications.
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