The
effects of coadsorbing the amphiphilic ruthenium-based dye
Z907 (cis-bis(isothiocyanato)(2,20-bipyridyl-4,40-dicarboxylato)(4,40-dinonyl-20-bipyridyl)ruthenium(II))
with the coadsorbent DPA (n-decylphosphonic
acid) and with the organic dye D35 ((E)-3-(5-(4-(bis(2′,4′-dibutoxybiphenyl-4-yl)amino)phenyl)thiophen-2-yl)-2-cyanoacrylic
acid) on mesoporous TiO2 were investigated using photoelectron
spectroscopy (PES). Z907 is expected to adsorb to the TiO2 surface via the carboxylic acid groups. However, Z907 also shows
signs of interacting with the TiO2 via the sulfur of the
thiocyanate groups, and this interaction is affected by both the addition
of DPA and D35. DPA, when added, exchanges with Z907 at the TiO2 surface, and each Z907 is replaced by six DPA molecules,
but it does not affect the energy level alignment between Z907 and
TiO2 substantially. Adding D35 to Z907 induces changes
in the adsorption configuration of Z907 by the means of suppressing
the interaction of the thiocyanate ligands and the TiO2 surface. The HOMO level of Z907 is shifted by the addition of D35.
Coadsorbing Z907 with D35 thus gives changes at a molecular level,
meaning that this is an example of collaborative sensitization.