Organic dyes incorporating low-band-gap chromophores based on π-extended benzothiadiazole for dye-sensitized solar cells

Abstract: A series of new π-conjugated organic dyes (HKK-BTZ1, HKK-BTZ2, HKK-BTZ3 and HKK-BTZ4), comprising triphenylamine (TPA) moieties as the electron donor and benzothiadiazole moieties as the electron acceptor/anchoring groups, was synthesized for the use in dye-sensitized solar cells (DSSCs). TPA units are bridged to benzothiadiazole with single(S), double(D) and triple bonds(T) in different derivatives. And HKK-BTZ1 was modified by introducing alkoxy group of TPA unit, because the bulky alkoxy group is a strong donating group for the more red shift and for reducing aggregation of dyes in TiO2 film. The structure-property relationship was investigated. Under standard global AM 1.5G illumination, a maximum photo-to-electron conversion efficiency of 7.30% was achieved with the DSSC based on dye HKK-BTZ4 (J SC =17.9mA/cm−2, V OC =0.62V, FF=0.66), while the Ru dye N719-sensitized DSSC showed an efficiency of 7.82% with a J SC of 17.5mA/cm−2, a V OC of 0.62V, and a FF of 0.72. [Copyright &y& Elsevier]