Organic solar cell dyes containing the most common anchoring group, cyanoacrylic acid, are shown to be photolabile and undergo photoisomerization. This may have significant consequences for dye-sensitized solar cells, as isomerisation competes with electron injection and leads to modifications of the dye and surface arrangement.

The structure of the dye layer adsorbed on the titania substrate in a dye-sensitized solar cell is of fundamental importance for the function of the cell, since it strongly influences the injection of photoelectrons from the excited dye molecules into the titania substrate. The adsorption isotherms of the N719 ruthenium-based dye were determined both with a direct method using the depth profiling technique neutral impact collision ion scattering spectroscopy (NICISS) and with the standard indirect solution depletion method. It is found that the dye layer adsorbed on the titania surface is laterally inhomogeneous in thickness and there is a growth mechanism already from low coverage levels involving a combination of monolayers and multilayers. It is also found that the amount of N719 adsorbed on the substrate depends on the titania structure. The present results show that dye molecules in dye-sensitized solar cells are not necessarily, as presumed, adsorbed as a self-assembled monolayer on the substrate.

Concentration depth profiles of the ruthenium based dyes Z907 and N719 adsorbed onto titania are measured directly and used for determining the adsorption isotherm of the dyes. Dye layers formed by both grow in islands on the titania which do not cover the entire titania surface even at the maximum coverage. Impedance spectroscopy in conjunction with the adsorption isotherms shows that recombination losses mainly appear between the dye and the electrolyte solution. The short circuit current and the efficiency increase linearly with the dye coverage. The open circuit voltage slightly increases with increasing dye coverage which is interpreted as most likely to be a consequence of the higher charge in the particles upon higher dye loading on the TiO2 surface.

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