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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.
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页码:6867 / 6872
页数:6
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