Combustion-synthesized sodium manganese (cobalt) oxides as cathodes for sodium ion batteries

被引:59
作者
Bucher, Nicolas [1 ,2 ]
Hartung, Steffen [1 ,2 ]
Gocheva, Irina [1 ]
Cheah, Yan L. [3 ]
Srinivasan, Madhavi [1 ,3 ]
Hoster, Harry E. [1 ,2 ]
机构
[1] TUM CREATE, Singapore 138602, Singapore
[2] Tech Univ Munich, D-85748 Garching, Germany
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
基金
新加坡国家研究基金会;
关键词
RECHARGEABLE LITHIUM BATTERIES; INTERCALATION ELECTRODES; ELECTROCHEMICAL-BEHAVIOR; ENERGY-STORAGE; NA; PHASE; CHALLENGES; SUBSTITUTION; DIFFRACTION; PERFORMANCE;
D O I
10.1007/s10008-013-2047-x
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
We report on the electrochemical properties of layered manganese oxides, with and without cobalt substituents, as cathodes in sodium ion batteries. We fabricated sub-micrometre-sized particles of Na0.7MnO2 + z and Na0.7Co0.11Mn0.89O2 + z via combustion synthesis. X-ray diffraction revealed the same layered hexagonal P2-type bronze structure with high crystallinity for both materials. Potentiostatic and galvanostatic charge/discharge cycles in the range 1.5-3.8 V vs. Na | Na+ were performed to identify potential-dependent phase transitions, capacity, and capacity retention. After charging to 3.8 V, both materials had an initial discharge capacity of 138 mA h g(-1) at a rate of 0.3 C. For the 20th cycle, those values reduced to 75 and 92 mA h g(-1) for Co-free and Co-doped samples, respectively. Our findings indicate that earlier works probably underestimated the potential of (doped) P2-type Na0.7MnO2 + z as cathode material for sodium ion batteries in terms of capacity and cycle stability. Apart from doping, a simple optimization parameter seems to be the particle size of the active material.
引用
收藏
页码:1923 / 1929
页数:7
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