文摘
The photostability of [RuII(bpy)2(4,4鈥?(PO3H2)2bpy)]Cl2 (bpy = 4,4鈥?bipyridine) on nanocrystalline TiO2 and ZrO2 films was investigated using a standard measurement protocol. Stability was evaluated by monitoring visible light absorbance spectral changes, in real time, during 455 nm photolysis (30 nm fwhm, 475 mW/cm2) in a variety of conditions relevant to dye-sensitized solar cells and dye-sensitized photoelectrosynthesis cells. Desorption (kdes) and photochemical (kchem) processes were observed and found to be dependent upon solvent, anion, semiconductor, and presence of oxygen. Both processes are affected by oxygen with kdes and kphoto noticeably smaller in argon saturated solution. Desorption was strongly solvent and pH dependent with desorption rates increasing in the order: methanol (MeOH) 鈮?acetonitrile (MeCN) < propylene carbonate (PC) < pH 1 pH 7. Photochemistry occurred in MeOH and PC but not in aqueous, 0.1 M HClO4 and MeCN. The anion and solvent dependence of kphoto strongly suggests the photoreaction involves ligand substitution initiated by population of metal centered d-d states. The relative stability of 鈭扨O3H2- versus 鈭扖OOH-substituted [RuII(bpy)3]2+ was also quantitatively established.
Keywords:
dye-sensitized solar cell (DSSC); dye-sensitized photoelectrosynthesis cell (DSPEC); ruthenium polypyridine; photostability; desorption; photochemistry