Abstract

Two copper complexes ([Cu(moby)2]2+/+ (moby=6,6′-bis(methoxymethyl)-2,2′-bipyridine) and [Cu(eoby)2]2+/+, (eoby=6,6′-bis(ethoxymethyl)-2,2′-bipyridine)) with bipyridine ligands were synthesized and used as redox mediators in dye-sensitized solar cells (DSSCs). The DSSCs exhibited high power conversion efficiencies of over 10% under simulated one sun irradiation (100 mW cm−2, AM 1.5G). The introduction of alkoxy groups onto the ligands effectively suppress charge recombination and increased the solubility of the copper complexes in acetonitrile, which led to the high photocurrent and stability of the DSSCs. The redox potentials of [Cu(moby)2]2+/+and [Cu(eoby)2]2+/+ were 0.65 and 0.70 V, respectively, whereas the open-circuit voltages of their DSSCs were still above 1.0 V. The relatively low redox potentials of the copper complexes enable them to match with more sensitizers to realize DSSCs with high photocurrent and photovoltage, providing an opportunity to further improve DSSCs by optimizing the copper redox mediator.

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