电化学
材料科学
阴极
扩散
离子
氧化物
相(物质)
结构稳定性
化学工程
过渡金属
兴奋剂
钠
纳米技术
电极
光电子学
化学
催化作用
冶金
物理化学
热力学
生物化学
物理
有机化学
结构工程
工程类
作者
Yi‐Hu Feng,Zhiwei Cheng,Chen‐Liang Xu,Lianzheng Yu,Duo Si,Boheng Yuan,Mengting Liu,Bin Zhao,Pengfei Wang,Xiaogang Han
标识
DOI:10.1021/acsami.2c03469
摘要
O3-NaNi0.25Fe0.5Mn0.25O2 layered oxide is considered one of the most promising cathode candidates for sodium-ion batteries because of its advantages, such as its large capacity and low cost. However, the practical application of this material is limited by its poor cyclic stability and insufficient rate capability. Here, a strategy to substitute the Fe3+ in NaNi0.25Fe0.5Mn0.25O2 with Al3+ is adopted to address these issues. The substitution of Fe3+ with Al3+ enhances the framework stability and phase transition reversibility of the parent NaNi0.25Fe0.5Mn0.25O2 material by forming a stronger TM–O bond, which improves the cycling stability. Moreover, partial Al3+ substitution increases the interslab distance, providing a spacious path for Na+ diffusion and resulting in fast diffusion kinetics, which lead to improved rate capability. Consequently, the target NaNi0.25Fe0.5–xAlxMn0.25O2 sample with optimal x = 0.045 exhibits a remarkable electrochemical performance in a Na-ion cell with a large reversible capacity of 131.7 mA h g–1, a stable retention of approximately 81.6% after cycling at 1C for 100 cycles, and a rate performance of 81.3 mA h g–1 at 10C. This method might pave the way for novel means of improving the electrochemical properties of layered transitional-metal oxides and provide insightful guidance for the design of low-cost cathode materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI