Study of spherical Li1.2-xNaxMn0.534Ni0.133Co0.133O2 cathode based on dual Li+/Na+ transport system for Li-ion batteries

Zhou, Y., Shan, W., Hou, X., Lam, K.-h. , Zhao, X., Liu, X. and Wu, Y. (2020) Study of spherical Li1.2-xNaxMn0.534Ni0.133Co0.133O2 cathode based on dual Li+/Na+ transport system for Li-ion batteries. Solid State Ionics, 350, 115326. (doi: 10.1016/j.ssi.2020.115326)

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Abstract

The Na-doped layered Li1.2-xNaxMn0.534Ni0.133Co0.133O2 (x = 0, 0.05, 0.1 and 0.15) cathode materials with porous spherical structure for lithium-ion batteries have been successfully prepared via a facile co-precipitation method. The dual Li+/Na+ transport system is Li1.2-xNaxMn0.534Ni0.133Co0.133O2 cathode materials companying with dual Li+/Na+ electrolyte, which exhibits an improved initial charge-discharge efficiency, cycling stability and rate capability, compared with pristine Li1.2Mn0.534Ni0.133Co0.133O2. Electrochemical results verify that Li1.1Na0.1Mn0.534Ni0.133Co0.133O2 delivers the initial charge/discharge capacity of 329.68/277.86 mAh g−1 with improved initial coulombic efficiency of 84.28% at 0.1C, and shows good cycling performance with a capacity retention of 76.5% after 100 cycles at 1C much higher than 37.9% of the pristine sample. Such outstanding performance of Li1.2-xNaxMn0.534Ni0.133Co0.133O2 is mainly attributed to: on the one hand, the small particle size and porous structure are helpful to increase the electrochemical active surface, shorten dual Li+/Na+ diffusion pathway, thus enhancing the energy storage properties. On the other hand, the design of dual Li+/Na+ transport system enables to enlarge interlayer, stabilize crystal structure and exert mutual diffusion or transportation of Li+ and Na+.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Lam, Dr Koko
Authors: Zhou, Y., Shan, W., Hou, X., Lam, K.-h., Zhao, X., Liu, X., and Wu, Y.
College/School:College of Science and Engineering > School of Engineering > Systems Power and Energy
Journal Name:Solid State Ionics
Publisher:Elsevier
ISSN:0167-2738
ISSN (Online):1872-7689
Published Online:29 April 2020
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