Structure studies on LiMn0.25Fe0.75PO4 by in-situ synchrotron X-ray diffraction analysis

被引:27
作者
Chen, Yi-Chun [1 ]
Chen, Jin-Ming [2 ]
Hsu, Chia-Haw [2 ]
Yeh, Jien-Wei [1 ]
Shih, Han C. [1 ,3 ]
Chang, Yee-Shyi [1 ]
Sheu, Hwo-Shuenn [4 ]
机构
[1] Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu 300, Taiwan
[2] Ind Technol Res Inst, Chutung 310, Taiwan
[3] Chinese Culture Univ, Inst Mat Sci & Nanotechnol, Taipei 111, Taiwan
[4] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
关键词
LiMPO4; In-situ XRD; Phase transformation; Olivine structure; LITHIUM BATTERIES; CATHODE MATERIALS; LIFEPO4; CATHODE; XRD; OLIVINES;
D O I
10.1016/j.jpowsour.2008.07.088
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
In this work, we substituted Mn2(+) at the 4c site of LiFePO4 to prepare LiMn0.25Fe0.75PO4 in order to raise the working voltage. In order to study the phase transformation of lithium bi-metal phosphate (LiM'M '' PO4) during the lithiation/delithiation, in-situ synchrotron X-ray diffraction has been used. At 0.05C charge/discharge, X-ray patterns reveal that LiMn0.25Fe0.75PO4 undergoes two two-phase transformations during the delithiation, resulting from Fe2+/Fe3+ and then Mn2+/Mn3+ redox reactions. However, the phase transformation for lithiation is different, becoming a two-phase (Mn2+/Mn3+) reaction and single-phase (Fe2+/Fe3+) reaction. Even at a higher charge/discharge rate (0.5C), the results are the same. LiMn0.25Fe0.75PO4 also has a good cyclability, since there is no significant capacity fading during the cycling test. The X-ray patterns reveal that LiMn0.25Fe0.75PO4 still maintains a good crystal structure after 40 cycles because of its stable olivine structure. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:790 / 793
页数:4
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