Organic dyes incorporating low-band-gap chromophores based on pi-extended benzothiadiazole for dye-sensitized solar cells
A series of new it-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 1.5 G illumination, a maximum photo-to-electron conversion efficiency of 7.30% was achieved with the DSSC based on dye HKK-BTZ4 (J(SC) = 17.9 mA/cm(-2). V-OC = 0.62 V, FF = 0.66), while the Ru dye N719-sensitized DSSC showed an efficiency of 7.82% with a J(SC) of 17.5 mA/cm(-2), a V-OC of 0.62 V, and a FF of 0.72. (C) 2011 Elsevier Ltd. All rights reserved.
Keywords: Metal-free organic dyes ; Low band-gap chromophore ; Benzothiadiazole unit ; Triphenylamine (TPA) unit ; pi-Bridge units ; Dye-sensitized solar cells ; Nanocrystalline Tio2 Electrodes ; Photovoltaic Performance ; Conversion-Efficiency ; Molecular Design ; Coumarin Dyes ; Light ; Derivatives ; Stability ; Injection ; Carboxyl
Record created on 2011-12-16, modified on 2016-08-09