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Bis(2,2′-bipyridine)bis(isothiocyanato)ruthenium complexes are organo-metallic dyes having broad absorption properties in the visible region that are widely used in dye-sensitized opto-electronic devices. Here, we report the photocurrent measurement and stability studies of three Ru-complexes,
cis
-bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)ruthenium(II) (
N3
), its hydrophobic analogues
cis
-bis(isothiocyanato)(2,2’-bipyridyl-4,4’-dicarboxylato)(4,4’-di-nonyl-2’-bipyridyl)ruthenium(II) (
Z-907
) and hydrophilic analogues (di-tetrabutylammonium
cis
-bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)ruthenium(II), (
N719
).
Z907
shows higher stability and photoelectric conversion efficiency after 2 h analysis than its hydrophilic counter-molecules,
N3
and
N719
. The
Z907
-TiO
2
system exhibited a 1.09 mA/cm
2
photocurrent density after 2 h of analysis, with 78% of its performance retained even after an extended 48 h of analysis. The activity of
N719
-TiO
2
and
N3
-TiO
2
sharply decreased after 2 h of analysis, and significant desorption of the dye present on titanium oxide was also observed. This study suggests that hydrophobicity at the electrode-dye interface is a major factor supporting the stability of the dye-sensitized photoanode.