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 in | Chinese chemical letters Vol. 24; no. 2; pp. 149 - 152 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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 |
Subjects | |
Online Access | Get full text |
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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%. |
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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 |