Electrochemical behavior of iron-substituted lithium nickelate

被引:72
作者
Prado, G [1 ]
Rougier, A
Fournès, L
Delmas, C
机构
[1] CNRS, Inst Chim Mat Condensee Bordeaux, F-33608 Pessac, France
[2] Ecole Natl Super Chim & Phys Bordeaux, F-33608 Pessac, France
关键词
D O I
10.1149/1.1393620
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Lamellar phases with nominal composition Li(Ni1-yFey)O-2 (y less than or equal to 0.30) were synthesized and characterized by Rietveld refinement of their X-ray diffraction (XRD) patterns. These materials exhibited the formula Li1-z(Ni1-yFey)(1+z)O-2 with 0.06 less than or equal to z less than or equal to 0.08 and were used as positive electrodes in lithium batteries. Their electrochemical performances decreased with increasing iron content. The Li-x(Ni0.90Fe0.10)(1.06)O-2 phases were characterized by XRD and Mossbauer spectroscopy. A solid solution appeared in the entire deintercalation domain 0.28 less than or equal to x less than or equal to 0.94, and Rietveld refinement of the XRD patterns allowed us to characterize the variation of structural parameters upon lithium deintercalation. Fe-57 Mossbauer spectroscopy showed that nickel and iron ions were oxidized simultaneously. The fraction of high-spin Fe4+ was related to the strong ligand field resulting from the presence of the prevailing Ni3+ and Ni4+ ions which lead to a lattice contraction. The behavior upon deintercalation of the Li(Ni0.90Fe0.10)O-2 phase was compared to that of two-dimensional LiFeO2. (C) 2000 The Electrochemical Society. S0013-4651(99)12-113-X. All rights reserved.
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页码:2880 / 2887
页数:8
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