Synthesis and photoelectric properties of an organic dye containing benzo[1,2-b:4,B-b']dithiophene for dye-sensitized solar cells

A novel benzodithiophene-containing organic dye BDT was synthesized and characterized as a sensitizer for a nanocrystalline TiO2-based dye-sensitized solar cell. Under simulated AM1.5G solar light (100mW/cm2) illumination, the DSC based on BDT gives a power conversion efficiency of 1.78%. A novel be...

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Published inChinese chemical letters Vol. 24; no. 2; pp. 149 - 152
Main Authors Gao, Yu-Rong, Chu, Ling-Ling, Guo, Wei, Ma, Ting-Li
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.02.2013
Dalian Research and Design Institute of Chemical Industry, Dalian 116023, China%State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China
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Summary:A novel benzodithiophene-containing organic dye BDT was synthesized and characterized as a sensitizer for a nanocrystalline TiO2-based dye-sensitized solar cell. Under simulated AM1.5G solar light (100mW/cm2) illumination, the DSC based on BDT gives a power conversion efficiency of 1.78%. A novel benzodithiophene-containing organic dye BDT was synthesized and characterized as a sensitizer for a nanocrystalline TiO2-based dye-sensitized solar cell. The BDT dye shows two major electronic absorptions. The absorption of the BDT dye covers a broad visible range from 300nm to 550nm. The benzodithiophene unit was used as a π bridge with several advantages: (1) It facilitates the electron transfer from the donor to the acceptor; (2) A facile structural modification on the 4,8-positions in the benzodithiophene unit can be achieved; (3) Fusing benzene with two flanking thiophene units improves the thermal stability. Under simulated AM1.5G solar light (100mW/cm2) illumination, the DSC based on BDT gives a power conversion efficiency of 1.78%.
Bibliography:DyesSolar cellsBenzodithiophenePower conversion efficiency
11-2710/O6
Received 7 September 2012 Received in revised form 27 November 2012 Accepted 11 December 2012 Available online 4 February 2013
ISSN:1001-8417
1878-5964
DOI:10.1016/j.cclet.2013.01.010