Evolution of local electronic and atomic structure of Co-doped LiMn2O4 cathode material for lithium rechargeable batteries

被引:22
作者
Hwang, BJ
Tsai, YW
Santhanam, R
Wu, YW
Hu, SG
Lee, JF
Liu, DG
机构
[1] Natl Taiwan Univ Sci & Technol, Microelect Chem Lab, Dept Chem Engn, Taipei 106, Taiwan
[2] Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
关键词
electronic structure; atomic structure XAS; Co-doped; LiMn2O4;
D O I
10.1016/S0378-7753(03)00516-0
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 situ X-ray absorption spectroscopy (XAS) techniques are performed to investigate the evolution of the local electronic and atomic structure of a spinel cathode material LiCO0.2Mn1.8O4 in the 4 V range. Changes in the oxidation state, bond distance, and local disorder of Mn and Co absorbers in the Co-doped LiMn2O4 are measured as a function of potentials. The X-ray absorption near edge spectra shows that charging (Li deintercalation) leads to the oxidation of manganese to Mn4+. On the other hand, Co atoms are also oxidized but the edge energy shift is small, which suggests that Co is also electroactive in LiCo0.2Mn1.8O4 in the 4 V range. The change in the Debye-Waller factor of the Co-O shell is smaller than that of Mn-O shell. Furthermore, from Debye-Waller factor and bond distance values, it appears that the Co environment fluctuates markedly during discharging. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:206 / 215
页数:10
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