Rational design of Na0.67Ni0.2Co0.2Mn0.6O2 microsphere cathode material for stable and low temperature sodium ion storage

材料科学 电化学 阴极 空位缺陷 相变 相(物质) 化学工程 过渡金属 扩散 氧化还原 动力学 容量损失 电极 结晶学 化学 冶金 物理化学 催化作用 热力学 物理 工程类 量子力学 有机化学 生物化学
作者
Xuan Wang,Xiuping Yin,Xiaochen Feng,Yong Li,Xiping Dong,Qinhao Shi,Yufeng Zhao,Jiujun Zhang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:428: 130990-130990 被引量:74
标识
DOI:10.1016/j.cej.2021.130990
摘要

Layered transition metal oxides with a classic composition of Na0.67Ni0.33Mn0.67O2 have attracted extensive attention due to their high specific capacity and suitable working voltage. However, its inherent structural defects can lead to a prone to phase change upon charging/discharging and cause degradation of electrochemical performance. In this work, a suitable Co-substituted Na0.67Ni0.2Co0.2Mn0.6O2 microsphere is designed and synthesized. The introduction of cobalt can effectively increase the interlayer spacing of transition metal oxides (TMO2), resulting in a faster Na+ diffusion kinetics. Such a structure enables the charge compensation from different redox couples (Ni2+/3+/4+, Co3+/4+ and Mn3+/4+), leading to a high specific capacity. Furthermore, the drawbacks of P2-O2 phase transition and Na+/vacancy ordering can be simultaneously restrained by a suitable content of Co substitution, which is confirmed by both cyclic voltammetry test and in-situ X-ray diffraction (XRD). The optimized Na0.67Ni0.2Co0.2Mn0.6O2 demonstrates a superior long-term cycle stability with a capacity retention rate of 83% over 200 cycles at 2 C. The electrochemical performance under extreme low-temperature (−40 °C) of this Na0.67Ni0.2Co0.2Mn0.6O2 material has also been explored for the first time, and the DNa+ values of this material can be maintained decently within a range from 10−11 to 10−10 cm2s−1. A high reversible discharge capacity of 132.2 mAh g−1 at 0.2 C is achieved at −40 °C, which is 80% of that at room temperature, indicating a satisfactory sodium storage performance at extremely low temperature.
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