Surface modification by suitable dyes of TiO2 electrodes used in photo
electrochemical cells allows noticeable increase of their photo-to-ele
ctrical conversion efficiency. Several bis or trisbipyridylruthenium(I
I) complexes, containing different functional groups (in particular, c
arboxylation of the pyridine ring is necessary to obtain a strong adso
rption) were studied. All of them were identified by ''normal'' (witho
ut any ''artificial'' enhancement) ex situ Raman spectroscopy. The dif
ferences (in peak position and intensity) of their spectra, typical of
the pyridine rings, carboxylated or not, yields the position of the m
olecule with respect to the oxide surface. It is the first time that s
uch a monolayer-on-oxide substrate was studied by Raman spectroscopy;
the laser light must stimulate the charge transfer in the Ti-molecule
surface complex.