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research article

Unsymmetrical squaraine dimer with an extended pi-electron framework: An approach in harvesting near infra-red photons for energy conversion

Kuster, Simon
•
Sauvage, Frederic  
•
Nazeeruddin, Md K.  
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2010
Dyes And Pigments

A fully conjugated unsymmetrical dimeric squaraine dye was synthesized. The synthetic key step for this dye, a selective Knoevenagel type condensation of end groups to the core moiety, allows the incorporation of a carboxylic acid function essentially for the strong coupling to the titanium dioxide (TiO2) surface. Moreover, the dimer exhibit outstanding optical properties such as absorption maximum in the NIR region with a huge molar absorption coefficient. The solvatochromic effects were also studied. Furthermore the electrochemical properties were determined with cyclic voltammetry. The reduction potential is just high enough to allow an efficient photo induced charge injection into the conduction band of the TiO2 semiconductor and the oxidation potential lies about 300 mV below the potential of the iodide / triiodide redox couple providing a good regeneration driving force. From electron density distribution calculations of the optimized BSQ01 structure we could see the directional charge displacement from the solvent exposed side in the HOMO to the carboxyl anchor group in the LUMO. The dimer was immobilised on TiO2 nanoparticles and a first dye sensitized solar cell was made as a proof-of-concept. (C) 2010 Elsevier Ltd. All rights reserved.

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Type
research article
DOI
10.1016/j.dyepig.2010.01.019
Web of Science ID

WOS:000278579500005

Author(s)
Kuster, Simon
•
Sauvage, Frederic  
•
Nazeeruddin, Md K.  
•
Graetzel, Michael  
•
Nueesch, Frank A.
•
Geiger, Thomas
Date Issued

2010

Publisher

Elsevier

Published in
Dyes And Pigments
Volume

87

Start page

30

End page

38

Subjects

Squaraine dye

•

Dimer

•

Synthesis

•

NIR-absorber

•

Molecular modelling

•

Dye sensitized solar cell

•

Sensitized Solar-Cells

•

Cyanine Dyes

•

Efficiency

•

Design

•

Films

Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LPI  
Available on Infoscience
September 14, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/53630
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