Electrochemical properties and structural evolution of O3-type layered sodium mixed transition metal oxides with trivalent nickel

被引:78
作者
Vassilaras, Plousia [1 ]
Kwon, Deok-Hwang [2 ]
Dacek, Stephen T. [1 ]
Shi, Tan [2 ]
Seo, Dong-Hwa [2 ]
Ceder, Gerbrand [1 ,2 ,3 ]
Kim, Jae Chul [3 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
CATHODE MATERIAL; HIGH-POWER; POSITIVE ELECTRODE; LITHIUM BATTERIES; ION BATTERIES; HIGH-ENERGY; INTERCALATION; DIFFUSION; DEINTERCALATION; STABILITY;
D O I
10.1039/c6ta09220a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical properties of NaNi0.5Co0.5O2 and NaNi0.5Fe0.5O2 and their structural transitions as a function of Na extraction associated with redox reactions are investigated in this work. Synthesized in the O3-type layered structure, both materials show reasonable electrochemical activities at room temperature, delivering approximately 0.5 Na per formula unit at C/10 discharge. More Na can be reversibly cycled in NaNi0.5Co0.5O2 at elevated temperature and/or in an extended voltage window, while NaNi0.5Fe0.5O2 shows significant capacity fading at a high voltage cutoff which is likely due to Fe4+ migration. In situ X-ray diffraction shows that the structural changes in the two materials upon desodiation are very different. NaNi0.5Co0.5O2 goes through many different two-phase reactions including three different O3-type and three different P3-type structures during cycling, producing a voltage profile with multiple plateau-like features. In contrast, NaNi0.5Fe0.5O2 has a smooth voltage profile and shows the typical O3-P3 phase transition without lattice distortion seen in other materials. This different structural evolution upon desodiation and re-sodiation can be explained by the electronic structure of the mixed transition metals and how it perturbs the ordering between Na ions differently.
引用
收藏
页码:4596 / 4606
页数:11
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