Based on the experimental observations that the three-phase nano-TiO2/F:SnO
2/I-/I-3(-) electrolyte front contact has to have pronounced rectifying pro
perties (reverse reaction with electrolyte suppressed) for efficient operat
ion of the dye-sensitization solar cell and plays an active part in the gen
eration of photoelectrochemical energy, an analytical formula is derived wh
ich allows the understanding of the relevance and involvement of a variety
of kinetic and cell parameters. Essentially, the TiO2 layer is treated as a
photocathode, donating electrons to a kinetically controlled front contact
, with the counter-charges being. transported by the electrolyte within the
pores. The formula was expanded to include photochemical kinetics of the s
ensitizer, for which photodegradation properties were also calculated. The
branching ratio, the ratio of regeneration-rate constant of the sensitizer
and of product-formation rate, turned out to be critical for long-term stab
ility. It may have to be improved by one order of magnitude for efficient c
ells to reach a lifetime of 20 years.
The degree of rectifying character of the nano-TiO2/F:SnO2/I-/I-3(-) electr
olyte interface (electric-field-dependent charge transfer to the front cont
act versus recombination-rate constant with I-3(-) distinguishes between a
low-efficiency ('dynamic') Galvani-type solar cell (efficiency determined b
y photoinduced chemical potential gradients, no rectifying contact) and a m
ore highly efficient 'junction-type' solar cell (separation and collection
of charges additionally assisted by junction potential). Several controvers
ial subjects are addressed. The key challenges for the improvement of such
cells are discussed, especially with respect to photodegradation and to sol
id-state devices.