A preparative route based on citrate precursors is used to obtain LiAlxCo1-
xO2 solid solutions over the whole composition range. From XRD, IR, and NMR
the compounds have been shown to be a substitution of Co by Al in the octa
hedral sites of the layer. A detailed Al-27, Co-59, and Li-7 MAS NMR study
is carried out on these products by using a high spinning speed in a high m
agnetic field (11.7 T). Aluminum is surrounded by six second-neighbor metal
s. Co/Al substitution leads to an almost regular chemical shift increment o
f +7 ppm, thus giving a maximum chemical shift of 62.5 ppm for the aluminum
surrounded by six cobalt atoms. This value is in the "classical" chemical
shift range of tetrahedral environments but is, however, characteristic of
an octahedral environment. Despite this unusual aspect of the Al-27 NMR che
mical shift, all the other NMR, XRD, and IR observations converge to a cons
istent description of the phase as being a continuous solid state solution
of octahedral sites randomly occupied by Co or Al. In the composition range
from 0 to 0.20 in Al it seems that the phase is a modified LiCoO2 type and
beyond 0.2 in Al looks like a ideal mixture. It is only beyond 0.9 that th
e phase more resembles LiAlO2.