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LaF sub(3)-coated Li[Li sub(0.2)Mn sub(0.56)Ni sub(0.16)Co sub(0.08)]O sub(2) as cathode material with improved electrochemical performance for lithium ion batteries
In this article, the pristine Li-rich layered oxide Li[Li sub(0.2)Mn sub(0.56)Ni sub(0.16)Co sub(0.08)]O sub(2) porous microspheres have been successfully synthesized using a urea combustion method and then coated with 1 wt% LaF sub(3) via a facile chemical precipitation route. The structures and mo...
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Published in: | RSC advances 2015-06, Vol.5 (63), p.50859-50864 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | In this article, the pristine Li-rich layered oxide Li[Li sub(0.2)Mn sub(0.56)Ni sub(0.16)Co sub(0.08)]O sub(2) porous microspheres have been successfully synthesized using a urea combustion method and then coated with 1 wt% LaF sub(3) via a facile chemical precipitation route. The structures and morphologies of both pristine and LaF sub(3) coated Li sub(1.2)Mn sub(0.54)Ni sub(0.16)Co sub(0.08)O sub(2) were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HR-TEM). The results reveal that the obtained particles possesses the morphology of porous microspheres and a LaF sub(3) layer with a thickness of 5-8 nm coated on the surface of the Li[Li sub(0.2)Mn sub(0.56)Ni sub(0.16)Co sub(0.08)]O sub(2) particles. As lithium ion battery cathodes, the LaF sub(3) coated sample, compared with the pristine one, has shown a significantly improved electrochemical performance; the initial coulombic efficiency improves from 75.36% to 80.01% and the rate compatibility increased from 57.4 mA h g super(-1) to an extremely high capacity of 153.5 mA h g super(-1) at 5 C. Decreased electrochemical impedance spectroscopy (EIS) reveals that the enhanced electrochemical performance of the surface coating was attributed to the lower charge transfer resistance of the sample. |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c5ra06243h |