4.5 Article

Evidence for structural defects in non-stoichiometric HT-LiCoO2:: electrochemical, electronic properties and 7Li NMR studies

Journal

SOLID STATE IONICS
Volume 128, Issue 1-4, Pages 11-24

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0167-2738(99)00335-5

Keywords

intercalation; lithium battery; LiCoO2; NMR; electronic conductivity

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HT-Lix(0)CoO(2) phases were synthesised via a solid state reaction with nominal Li/Co ratios x(0) = 0.90, 1.0, 1.05 and 1.10. These materials were studied by X-ray and neutron diffraction, galvanostatic lithium intercalation/deintercalation and electrical measurements as well as Li-7 MAS NMR spectroscopy. While the galvanostatic charge curve of the stoichiometric material shows a voltage plateau at ca. 3.93 V for 0.75 less than or equal to x less than or equal to 0.94 and a particular feature for Li0.5CoO2 (x(0) = 1.0) due to a monoclinic distortion, the charge curves of materials with x, = 1.05 and 1.10 do not present the voltage plateau nor the monoclinic distortion. XRD studies show the occurrence of a solid solution in the 0.60 less than or equal to x less than or equal to 1.10 domain. Li-7 MAS NMR spectra of Lix(0)CoO(2) materials with x(0) > 1 exhibit three new signals at 190, - 18 and - 40 ppm in addition to the signal at 0 ppm resulting from the presence of diamagnetic Co-III. A Li-7 MAS NMR study of the materials obtained by electrochemical deintercalation and reintercalation of lithium from Li1.10CoO2 shows that these new features do not arise from lithiated surface species or from interstitial Li+. On the basis of our general knowledge of Li NMR in comparable materials with electron spins, we suggest the presence of paramagnetic low-spin Co-II and of a simultaneous cobalt and oxygen deficiency in samples with x(0) > 1.0. (C) 2000 Elsevier Science B;V. All rights reserved.

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