Synthesis of ruthenium complex and its application in dye-sensitized solar cells

An amphiphilic bipyridyl ligand, 4,4′-dicarboxy-octyl-2,2′-bipyridine, and its ruthenium(□) complex (termed as S8) were synthesized and characterized by UV/Vis, IR and NMR spectroscopy. The performance of this S8 complex as charge transfer photo-sensitizer in TiO 2-based dye-sensitized solar cells was studied under standard AM 1.5 sunlight and by using an electrolyte consisting of 0.70 M 1,2-dimethyl-3-propyl-imidazolium iodide, 0.10 M LiI, 40 mM iodine and 0.125 M 4-tert-butylpyridine in acetonitrile. Aliphatic chains linking to carboxylate groups of S8 act as an effective electron donor and carboxylate groups act as an effective electron withdrawing between the TiO 2 layer and the carboxylate linking TiO 2 layer leading to increasing of electron density at this interface, which is attributed to increasing efficiency of electron injection to the TiO 2 conduction band from the excited state of dye. The complex, S8, gave a photocurrent density of 13.02 mA/cm 2, 0.60 V open circuit voltage and 0.69 fill factor yielding 5.36% efficiency. The S8 dye with aliphatic chain improved conversion efficiency of the resulting DSSCs compared with a cell fabricated using the N3 dye.