Abstract
Low temperature synthesis of the Lithium-rich cubic spinel Li4Mn5O12 with an oxidation state very close to +4 is described. The effect of doping this compound with cobalt according to the solid solution mechanism Li4-xMn5-2xCo3xO12 up to the solid solution limit, LiMnCoO4, has also been explored. The evolution of the structure and electrochemistry with increasing cobalt doping is described. With increasing x there is increasing population of the tetrahedral 8a site by transition metal ions reaching 25% occupancy by Co at LiMnCoO4 with corresponding displacement of Li to 16d sites. The optimum performance was obtained for die composition Li3.75Mn4.5Co0.75O12 which yields a capacity of 250 mA g(-1) at a rate of 25 mA g(-1) (equivalent to C/6) with no perceptible capacity loss, in sharp contrast to the pure Mn materials. (C) 2001 Elsevier Science B.V. All rights reserved.
Original language | English |
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Pages (from-to) | 332-335 |
Number of pages | 4 |
Journal | Journal of Power Sources |
Volume | 97-98 |
Publication status | Published - Jul 2001 |
Keywords
- lithium batteries
- lithium-rich cubic spinel
- lithium intercalation
- ELECTROCHEMICAL PERFORMANCE
- INTERCALATION CATHODES
- LIMN2O4
- ELECTRODES
- LI4MN5O12
- INSERTION
- PHASE