材料科学
锑
阴极
相(物质)
钠离子电池
电化学
钠
离子
分析化学(期刊)
相变
电极
物理化学
化学
热力学
法拉第效率
冶金
有机化学
物理
色谱法
作者
Lianzheng Yu,Xuanxuan Xing,Siyuan Zhang,Xiaoyan Zhang,Xiaogang Han,Pengfei Wang,Sailong Xu
标识
DOI:10.1021/acsami.1c06576
摘要
O3-type sodium-layered oxides (such as antimony-based O3 structures) have been suggested as one of the most fascinating cathode materials for sodium-ion batteries (SIBs). Honeycomb-ordered antimony-based O3 structures, however, unsatisfactorily exhibit complex phase transitions and sluggish Na+ kinetics during cycling. Herein, we prepared a completely cationic-disordered O3-type Na0.8Ni0.6Sb0.4O2 compound by composition regulation for SIBs. Surprisingly, the measured redox potentials for typical O3–P3 phase transition are located at 3.4 V. Operando X-ray diffraction confirms a reversible phase transition process from the O3 to P3 structure accompanied with a very small volume change (1.0%) upon sodium extraction and insertion. The low activation barrier energy of 400 meV and the fast Na+ migration of 10–11 cm2·s–1 are further obtained by first-principles calculations and galvanostatic intermittent titration technique, respectively. As a result, the O3-Na0.8Ni0.6Sb0.4O2 cathode displays a reversible capacity of 106 mA h g–1 at 0.1C (12 mA g–1), smooth charge–discharge curves, and a high average working voltage of 3.5 V during battery cycling. The results highlight the importance of searching for a new O3-type structure with cation-disordering and high working voltage for realizing high energy SIBs.
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