Optimizing the Photocurrent Efficiency of Dye-Sensitized Solar Cells through the Controlled Aggregation of Chalcogenoxanthylium Dyes on Nanocrystalline Titania Films

Abstract

Chalcogenoxanthylium dyes were characterized as sensitizers of nanocrystalline titania in dye-sensitized solar cells (DSSCs). Four series of dyes were characterized: 2,7-bis(dimethylamino)-9-(2-thienyl-5-carboxy)chalcogenoxanthylium dyes ( 1-E, where E = O, S, Se); 2,7-bis(dimethylamino)-9-(3-thienyl-2-carboxy)chalcogenoxanthylium dyes ( 2-E, where E = S, Se); a 2,7-bis(dimethylamino)-9-(2-thienyl)selenoxanthylium dye ( 3-Se ); 4-Se, a constrained analog of 1-Se . The orientation and aggregation state of the dyes were controlled by varying the position of the surface-attachment group relative to the xanthylium core. Series 1 dyes and 4-Se underwent H-aggregation on titania surfaces, whereas series 2 dyes adsorbed in amorphous monolayers. ( 3-Se did not adsorb appreciably to titania films, due to the lack of a tethering group.) The H-aggregated dyes exhibited broader absorption bands, increased light-harvesting efficiencies, and improved photoelectrochemical performance compared to the dyes which adsorbed in amorphous monolayers. The maximum incident photon-to-current efficiencies (IPCEs) of series 1 dyes ranged from 70% to 84%, whereas those of 2-S and 2-Se were 11% and 20%. Our findings reveal that the light-harvesting efficiency, IPCE, and absorbed photon-to-current efficiency (APCE) of DSSCs with organic dyes can be optimized by systematically varying the structure of the dyes and their orientation and aggregation state on the surface.