A molybdenum doped layer-spinel composite cathode material for sodium-ion battery

被引:3
|
作者
Vanam, Sai Pranav [1 ]
Barpanda, Prabeer [1 ,2 ,3 ]
机构
[1] Indian Inst Sci, Mat Res Ctr, Faraday Mat Lab FaMaL, Bangalore 560012, India
[2] Helmholtz Inst Ulm HIU, Electrochem Energy Storage, D-89081 Ulm, Germany
[3] Karlsruhe Inst Technol KIT, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
Sodium -ion battery; P2-layer; spinel composite; P2-P2? phase transition; OXYGEN; CHEMISTRY; ELECTRODE;
D O I
10.1016/j.electacta.2022.141122
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Sodium-ion batteries are pursued as pragmatic alternative to the Li-ion battery technology having operational similarity along with natural resource abundance. P2-type manganese-rich layered oxides are widely explored exhibiting high capacity along with fast rate kinetics. To improve their electrochemical performance and reduce voltage decay upon cycling and to mitigate irreversible phase transitions, cation doping or hybrid composite integrations have been proposed. Here, we report a unique Mn-rich layer-spinel composite, Na0.7(Li1/18Mn11/ 18Ni3/18Fe2/18 chi 1/18)O2-xNa2MoO4, leading to a synergistic effect of layered P2 and spinel phases. This stable layer/spinel biphasic composite was stabilized through Mo doping and its electrochemical activity was studied at different voltage windows. When cycled between 1.5-4.5 V, this composite delivered a high specific capacity of 183 mAh.g-1 involving both cationic and anionic (O2-/O2n-) redox. The structural evolution during (dis)charge was studied by ex-situ X-ray diffraction and cyclic voltammetry. It is observed that mitigating P2-P2 '' phase transition at higher voltage is crucial to improve the electrochemical performance, cycling stability and reduce the voltage hysteresis.
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页数:8
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