Triphenylamine- and benzothiadiazole-based dyes with multiple acceptors for application in dye-sensitized solar cells

Two novel dyes TPAR3 and BTDR2 based on triphenylamine and benzothiadiazole, respectively, with multiple electron acceptors were synthesized and characterized by FT-IR, 1H NMR, TGA and thermomechanical analysis (TMA). They carried terminal cyanoacrylic acid electron acceptors/anchoring moieties, whi...

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Published inJournal of power sources Vol. 195; no. 9; pp. 3002 - 3010
Main Authors Mikroyannidis, John A., Suresh, P., Roy, M.S., Sharma, G.D.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.05.2010
Elsevier
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Summary:Two novel dyes TPAR3 and BTDR2 based on triphenylamine and benzothiadiazole, respectively, with multiple electron acceptors were synthesized and characterized by FT-IR, 1H NMR, TGA and thermomechanical analysis (TMA). They carried terminal cyanoacrylic acid electron acceptors/anchoring moieties, which were connected with the central unit through a thiophene ring. The absorption bands of the dyes were extended up to ∼570 nm with long-wave absorption maximum at 425–455 nm and optical band gap of 2.10–2.17 eV. The dyes emitted yellow–orange light with photoluminescence maximum at 547–615 nm. We have investigated the photovoltaic properties of quasi solid state dye sensitized solar cells (DSSCs) based on these metal free organic dyes. It has been found that the power conversion efficiency of the DSSCs based on composite zinc titanium oxide (ZTO) nanocrystalline photoelectrode is higher than that for TiO 2 based DSSCs. This has been attributed to the longer electron lifetime and more negative conduction band edge of ZTO. The overall power conversion efficiency of the DSSCs based on TPAR3 and BTDR2 employing ZTO photoelectrode is 6.3% and 3.6%, respectively. These results indicate that both the acceptor moiety of metal free organic dyes and ZTO photoelectrode have an effect on the photovoltaic performance of DSSCs.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2009.10.107