Chem. Mater., 20 (5), 18301840, 2008. 10.1021/cm702631r
Web Release Date: February 5, 2008

Copyright © 2008 American Chemical Society

2,3-Disubstituted Thiophene-Based Organic Dyes for Solar Cells

K. R. Justin Thomas, Ying-Chan Hsu, Jiann T. Lin,* Kun-Mu Lee,§ Kuo-Chuan Ho,*§ Chin-Hung Lai, Yi-Ming Cheng, and Pi-Tai Chou*

Institute of Chemistry, Academia Sinica, Taipei 115, Taiwan, Department of Chemistry, National Central University, Chungli 320, Taiwan, and Departments of Chemical Engineering and Chemistry and Institute of Polymer Science and Engineering, National Taiwan University, Taipei 106, Taiwan

Received September 14, 2007

Revised Manuscript Received November 22, 2007

Abstract:

New organic dyes that contain variable lengths of conjugation, featuring oligothiophene and arylamines at the 2- and 3-position, have been synthesized. These compounds are characterized by photophysical, electrochemical, and theoretical computational methods. Nanocrystalline TiO2-based dye-sensitized solar cells were fabricated using these molecules as light-harvesting sensitizers. The overall efficiencies of the sensitized cells range from 4.11 to 6.15%, compared to a cis-di(thiocyanato)-bis(2,2′-bipyridyl)-4,4′-dicarboxylate ruthenium(II)-sensitized device (7.86%) fabricated and measured under similar conditions. The devices made from these compounds have higher open-circuit voltage (VOC) compared to oligothiophene congeners with arylamines at the 2-position only. The hydrophobic segment at the 3-position appears to help retarding the charge transfer from the conduction band of TiO2 to the electrolyte, I3. Supplementary studies of the transient photovoltage and electrochemical impedance are in support of retarded charge transfer of TiO2 (e) with both oxidized sensitizer and I3. Computation on a pair of compounds with and without arylamines at 3-position indicates that the former has larger charge transfer efficiency at the electronically excited state.

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