4.8 Article

Electrochemical and structural studies of LiCo1/3Mn1/3Fe1/3PO4 as a cathode material for lithium ion batteries

Journal

JOURNAL OF POWER SOURCES
Volume 195, Issue 19, Pages 6867-6872

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2010.01.058

Keywords

Olivine structure; Synchrotron X-ray; diffusivity; Lithium multi-transition metal phosphate

Funding

  1. National Science Council of the Republic of China [NSC95-2221-E007-042]

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A solid-state reaction to synthesize a lithium multi-transition metal phosphate LiCo1/3Mn1/3Fe1/3PO4 is used in this work, which has a high voltage of 3.72 V and capacity of 140 mAh g(-1) at a 0.05 C rate. From the in-situ XRD analysis, LiCo1/3Mn1/3Fe1/3PO4 has shown a high stability during cell charge/discharge, even operating at 5 V, which is due to the stable olivine structure. Although all the transition metals Co2+, Mn2+ and Fe2+ are at the same 4c site of the LiCo1/3Mn1/3Fe1/3PO4 structure, they seem to have different chemical activities and reflect on the electrochemical performance. The capacity contributed by the Co2+/Co3+ redox couple is only 20 mAh g(-1), which is less than that of the Fe2+/Fe3+ and Mn2+/Mn3+ redox couples. This is because of the fact that the diffusivity of lithium ion for the Co2+/Co3+ redox couple is 10(-16) cm(2) s(-1) which is one order less than that of the Fe2+/Fe3+ and Mn2+/Mn3+ redox couples in LiCo1/3Mn1/3Fe1/3PO4. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.

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