电化学
循环伏安法
阴极
兴奋剂
掺杂剂
离子
材料科学
钠
过渡金属
扩散
滴定法
电极
分析化学(期刊)
化学工程
无机化学
化学
光电子学
物理化学
冶金
催化作用
工程类
热力学
有机化学
物理
生物化学
色谱法
作者
Ningyun Hong,Kang Wu,Zhengjun Peng,Zenghu Zhu,Guofeng Jia,Min Wang
标识
DOI:10.1021/acs.jpcc.0c06032
摘要
O3-type layered transition metal oxides have shown great promise as high-capacity cathode materials for sodium-ion batteries in large-scale energy storage, due to their low cost and the abundance of sodium resources. However, the limited interlayer spacing and the unstable structure of the O3 phase result in inferior cycling stability and poor rate capability, which could even hinder their practical application process. Hereby, we present that doping with nonelectrochemically active Al in NaAlx(Ni0.5Mn0.5)1–xO2 (x = 0, 0.02, 0.06, 0.1) can effectively alleviate these issues. Among these materials, materials with x = 0.02 exhibited the best electrochemical behavior with improved capacity and better cycling property than other materials. Specifically, the discharge capacity of a 2 mol % Al-doped material possesses 63.2% capacity retention after 200 cycles at a current density of 240 mA g–1, which is 21.4% higher than that in NaNi0.5Mn0.5O2. In addition, a 2 mol % Al-doped electrode also shows outstanding rate capability and delivers 90 mAh g–1 at a high rate of 480 mA g–1, compared to only 67 mAh g–1 for that of the pristine one. X-ray diffraction (XRD), cyclic voltammetry (CV), and galvanostatic intermittent titration technique (GITT) analysis elucidated that the introduced Al dopant can effectively improve the structural stability and promote kinetics of Na+ diffusion mobility. Therefore, the strategy of doping inactive aluminum elements for optimizing the electrochemical performance of NaNi0.5Mn0.5O2 was verified, which could also open an avenue for the design of other O3-type sodium cathode materials.
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