Nanocrystalline particles of ZnO
and TiO
2 of approximately equal size (~15 nm) were used to preparemesoporous electrodes for dye-sensitized solar cells. Electron transport in the solar cells was studied usingintensity-modulated photocurrent spectroscopy
and revealed very similar results for ZnO
and TiO
2. Apparentactivation energies for electron transport in nanostructured ZnO of
0.1 eV were calculated from thetemperature dependence of transport times under short-circuit conditions. The lifetime of electrons in thenanostructured semiconductors was evaluated from open-circuit voltage decay
and intensity-modulatedphotovoltage spectroscopy. Significantly longer lifetimes were obtained with ZnO. Despite the reducedrecombination, ZnO-based solar cells performed worse than TiO
2 cells, which was attributed to a lower electroninjection efficiency from excited dye molecules
and/or a lower dye regeneration efficiency. The internalvoltage in the nanostructured ZnO film under short-circuit conditions was about 0.23 V lower than the open-circuit potential at the same light intensity. Results may be explained using a multiple trapping model, but aselectrons are usually only shallowly trapped in ZnO, an alternative view is presented. If there is significantdoping of the ZnO, resulting b
and bending in the nanocrystals will form energy barriers for electron transport
and recombination that can explain the observed properties.