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

被引:28
作者
Chen, Yi-Chun [1 ]
Chen, Jin-Ming [2 ]
Hsu, Chia-Haw [2 ]
Lee, Jey-Jau [3 ]
Lin, Tsung-Chi [4 ]
Yeh, Jien-Wei [1 ]
Shih, Han C. [1 ,4 ]
机构
[1] Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu 300, Taiwan
[2] Ind Technol Res Inst, Chutung 310, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
[4] Chinese Culture Univ, Inst Mat Sci & Nanotechnol, Taipei 111, Taiwan
关键词
Olivine structure; Synchrotron X-ray; diffusivity; Lithium multi-transition metal phosphate; X-RAY-ABSORPTION; LIFEPO4; OLIVINES; FE; LIMN0.25FE0.75PO4; ELECTRODES; BEHAVIOR; ENERGY; CARBON;
D O I
10.1016/j.jpowsour.2010.01.058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:6867 / 6872
页数:6
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