P. Ganguly et al., ENVIRONMENT DEPENDENCE OF METAL OR LIGAND OXIDATION IN COPPER-OXIDE SYSTEMS - EVIDENCE FROM HEATS OF FORMATION AND LI-7 SOLID-STATE NMR-STUDIES, Journal of physical chemistry, 100(12), 1996, pp. 5017-5024
The stability of the Cu3+ ion in an oxide matrix such as La(2)Li(0.5)M
(0.5)(3+)O(4) (M = Cu, Ni, or Co) or La2-xSrxCu1-yLiyO4 (x = 0 or 0.15
, y = 0 or 0.025) is examined. Heats of formation (as measured by solu
tion calorimetry) and Li-7 NMR have been used for this purpose. I:rom
the systematic nature of the reported heats of formation of binary com
pounds analyzed per ligand X ion, Delta H-X, arguments are presented f
or the existence of a maximum value of Delta H-X corresponding to a ma
ximum ionicity (similar to 660 kJ/g at X). A scheme is then proposed t
o extract the heat of formation per oxygen, Delta H(Cu)(O), in the CuO
1+delta component of ternary copper oxides of metals such as La, Ba, L
i, etc. which have Delta H-O close to the maximum value. We then find
that the value of Delta H(Cu)(O) in La2Li0.5Mo0.53+O4 (similar to 400
kJ/g at O) is very large relative to that in CuO (similar to 165 kJ/g
at O) and suggests an ionic Cu3+-O2- linkage (metal oxidation). In La2
-xSrxCuO4 the low value of Delta H(Cu)(O) is consistent with considera
ble O --> Cu charge transfer and creation of holes on oxygen. These co
nclusions are supported by Li-7 NMR studies which probe the local envi
ronment in the CuO matrix. Advantage is taken of the paramagnetic shif
ts of the resonance frequency in such anisotropic systems and the dual
principal axes (quadrupolar and magnetic dipolar) interaction tensors
to understand the Li-7 NMR. The main results of the NMR study are tha
t in La(2)Li(0.5)M(0.5)O(4) systems the quadrupolar splitting of the L
i-7 is nearly constant for all M ions indicating a similar LiO6 enviro
nment. When coupled with the Delta H(M)(O) data, this implies that the
re is little O --> M charge transfer. In La2-xSrxCu1-yLiyO4 on the oth
er hand the Li-7 NMR shows three kinds of environments for the Li ions
despite there being only a single crystallographic site. We suggest t
hat at least one of these environments is due to the creation of holes
on oxygen.