Journal
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 150, Issue 4, Pages A403-A413Publisher
ELECTROCHEMICAL SOC INC
DOI: 10.1149/1.1554911
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We examined the evolution of the oxidation state and atomic structure of V in nanophase V2O5 aerogel and ambigel cathodes under in situ conditions using X-ray absorption spectroscopy (XAS). We show that the oxidation state of V in V2O5 aerogel and ambigel cathodes heated under vacuum (100 muTorr) at 220degreesC for 16 h is similar to that of V in a commercially obtained sample of orthorhombic V2O5. However, the local structure of V in aerogel and ambigel V2O5 has a higher degree of local symmetry relative to orthorhombic V2O5 and/or the average V-O bond length is greater than that of orthorhombic V2O5. Furthermore, we show that during the first cycle of discharge, the degree of Li insertion (x in Li-x V2O5) for the ambigel cathode is greater than that of the aerogel cathode (x = 3.06 for the ambigel cathode compared to x = 2.68 for the aerogel cathode) for the same cut-off voltage. Accordingly, the observed V K-edge energy shift for the fully discharged ambigel cathode is greater than that observed for the fully discharged aerogel cathode, and hence, the extent of reduction of pentavalent V is greater for the ambigel cathode. In both cases, the extent of reduction of the V is consistent with the amount of Li inserted (i.e., Li-x V2O5). Initially, pentavalent V is reduced to tetravalent V in the intercalation range 0 < x < 2 and then tetravalent V is reduced to trivalent V upon insertion of more Li (x > 2). Analyses of Fourier transform data reveal that V has a higher degree of local symmetry in the discharged state relative to that of the charged state. (C) 2003 The Electrochemical Society.
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