Recent thermodynamic and electrical conductivity data are evaluated to sele
ct the most appropriate electrolyte composition for IT-SOFC operation at 50
0 degrees C. Ce0.9Gd0.1O1.95 has an ionic lattice conductivity of 10(-2) S
cm(-1) at 500 degrees C, and the Gd3+ ion is the preferred dopant, compared
to Sm3+ and Y3+, at this temperature. Thermodynamic investigations indicat
e that for CeO2-Re2O3 solid solutions at intermediate temperatures it becom
es easier to reduce Ce4+ as the concentration of Re2O3 is increased. As the
associated electron mobilities do not appear to be a strong function of co
mposition it follows that Ce0.9Gd0.1O1.95 has a wider ionic domain than Ce0
.8Gd0.2O1.9 at intermediate temperatures. particular attention is drawn to
the deleterious effects of impurities (principally SiO2) which are responsi
ble for large dopant concentration dependent grain boundary resistivities.
These grain boundary resistivities can obscure the intrinsic lattice ionic
conductivities and cause investigators to select non-optimal dopant composi
tions. It follows that the use of clean (SiO2 < 50 ppm) powders is strongly
recommended, particularly as these are now commercially available. At pres
ent there is also no compelling evidence to confirm that the intrinsic latt
ice electronic conductivity is significantly changed by co-doping with Pr6O
11. Finally the I-V characteristics of single cells incorporating 25-mu m t
hick Ce0.9Gd0.1O1.95 electrolytes are modelled, and the requirements for co
mposite electrodes briefly discussed so that power densities of 0.4 W cm(-2
) at 500 degrees C can be attained. (C) 2000 Elsevier Science B.V. All righ
ts reserved.