Effects of Na+ contents on electrochemical properties of Li1.2Ni0.13Co0.13Mn0.54O2 cathode materials
The Li1.2−xNaxNi0.13Co0.13Mn0.54O2 (0≤x≤0.1) cathode materials have been synthesized by a solid-state reaction method. The effects of the Na+ contents on the structure, surface components and electrochemical performance are studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) a...
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Published in | Journal of power sources Vol. 240; pp. 530 - 535 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.10.2013
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The Li1.2−xNaxNi0.13Co0.13Mn0.54O2 (0≤x≤0.1) cathode materials have been synthesized by a solid-state reaction method. The effects of the Na+ contents on the structure, surface components and electrochemical performance are studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electrochemical techniques. The XRD data indicate that the Li1.2−xNaxNi0.13Co0.13Mn0.54O2 samples evolve from a sole layered structure (0≤x≤0.02) to a mixture of Na+-contained layered structure (0.02<x≤0.1), which would transform into the single layered structure after the initial charge and discharge process. XPS data demonstrate that some of the Na+ ions could be reversibly de-/re-intercalated for the Li1.2−xNaxNi0.13Co0.13Mn0.54O2 materials. An electrochemical test reveals that a small amount of Na+ (x≤0.02) in the Li1.2−xNaxNi0.13Co0.13Mn0.54O2 materials can significantly increase the rate capacity, yet the capacity retention becomes worse. We also find that the capacity retention increases with the Na+ contents.
•A small amount of Na+ can significantly increase the initial discharge capacity.•Some of the Na+ ions could be reversibly de-/re-intercalated from the electrodes.•The structure evolves from a solely layered structure to a mixture of layered structure.•It could explain how the sodium species impact on the electrochemical performance. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2013.04.047 |