The battery cathode material LiCoO2 was synthesized with a deliberate
excess of Li, according to Li1+yCoO2, where y = 0.08 and 0.35 (nominal
ly). The effect of divalent doping with Mg2+ was also explored for som
e samples, with y values of 0.0 (stoichiometric) and 0.08. Electrical
conductivity measurements of the stoichiometric material, without Mg,
as functions of oxygen partial pressure and temperature exhibit p-type
semiconducting behaviour and suggest that the defects primarily respo
nsible for the generation of holes are cobalt ion vacancies. Excess Li
increases the electrical conductivity, while the incorporation of Mg
leads to a more dramatic enhancement in conductivity, the latter inter
preted as a transition to metallic behaviour. NMR spectroscopic measur
ements of both Li-6,Li-7 isotopes suggest that only a small fraction (
< 20%) of the excess Li in the y = 0.35 material enters the structure
ionically while reducing the formal Co valence. Most of the excess con
sists of Li2CO3 and possibly other impurity phases, the former also ha
ving been identified by X-ray diffraction. Another small portion of th
e excess Li (about 10%) appears to enter interstitial sites in close p
roximity to paramagnetic Co2+ ions.