Synchrotron X-ray absorption study of LiFePO4 electrodes

被引:73
作者
Haas, O [1 ]
Deb, A
Cairns, EJ
Wokaun, A
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
关键词
D O I
10.1149/1.1833316
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LiFePO4 was investigated in practical Li-ion intercalation electrodes used for Li-ion batteries by applying X-ray absorption spectroscopy (XAS). A special in situ XAS cell was constructed to charge and discharge the LiFePO4 electrodes at current densities typically used in Li-ion batteries. Ex situ XAS measurements were made with technically relevant electrodes developed by Hydro-Quebec power research using LiPF6 as an electrolyte and ethylene carbonate/dimethyl carbonate as a solvent. The X-ray absorption spectra were measured at the initial state [containing mainly LiFePO4, Fe(II)], which corresponds to the uncharged state of the battery and at the delithiated state [FePO4, Fe(III)], which corresponds to the battery's charged state. The X-ray absorption near-edge structure region of the X-ray absorption spectra showed a substantial Fe K-edge shift after the electrode was electrochemically oxidized. The pre-edge features of the X-ray absorption spectra revealed high spin configuration for the two oxidation states [Fe(II), d(6) and Fe(III), d(5)]. Reasonable ligand field stabilization energies could be extracted from the pre-edge features. Using the data analysis program EXAFSPAK with the FEFF8 code provided in this program, the EXAFS spectrum and its Fourier transformed radial structure function could be simulated satisfactorily, where only single scattering paths were used for this simulation. (C) 2004 The Electrochemical Society.
引用
收藏
页码:A191 / A196
页数:6
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