Cobalt-substituted Na0.44Mn1-xCoxO2: phase evolution and a high capacity positive electrode for sodium-ion batteries

被引:46
作者
Zhou, Yu-Ting [1 ,2 ]
Sun, Xin [1 ,2 ]
Zou, Bang-Kun [1 ,2 ]
Liao, Jia-Yin [1 ,2 ]
Wen, Zhao-Yin [3 ]
Chen, Chun-Hua [1 ,2 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Mat Energy Convers, Dept Mat Sci & Engn, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Anhui, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
sodium ion battery; phase evolution; layered structure; sodium manganese oxide; cobalt doping; CATHODE MATERIALS; ENERGY-STORAGE; NA0.44MNO2; CHALLENGES; OXIDE; INTERCALATION; NANOWIRES;
D O I
10.1016/j.electacta.2016.07.089
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Na0.44Mn1-xCoxO2 (x = 0, 0.01, 0.08, 0.11, 0.22, 0.33, 0.44) powders are synthesized as positive electrodes for sodium-ion batteries via a thermopolymerization method. X-ray diffraction and scanning electron microscopy are used to analyze their crystal structures and particle morphologies. Galvanostatic cell cycling is used to characterize the electrochemical properties. The Co-substitution can change the structure of Na0.44Mn1-xCoxO2 from T-type (x = 0) into layered P2-type (x = 0.11) or P3-type (x = 0.44). For the samples synthesized under our specific conditions, the particle morphology can be used as an indicator of their crystal structures: rod-like (T-type), plate-like (P2-type) and granules (P3-type). P2-type Na0.44Mn0.89Co0.11O2 allows more Na+ intercalation into the inter-layer spacing and results in a high discharge capacity with 220 mAh g (1) at 12 mA g (1) in initial cycle, 180 mAh g (1) after 40 cycles in the voltage range of 2.0-4.2 V and a good rate performance of 104 mAh g (1) at a rate of 600 mA g (1) in the voltage range of 2.0-4.0 V. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:496 / 503
页数:8
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