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New D-A-D-A-D push-pull organic semiconductors with different benzo[1,2-b:4, 5-b '] dithiophene cores for solution processed bulk heterojunction solar cells

Authors
Do, KwangseokCho, NaraSiddiqui, S. A.Singh, Surya PrakashSharma, Ganesh D.Ko, Jaejung
Issue Date
9월-2015
Publisher
ELSEVIER SCI LTD
Keywords
Push-pull organic semiconductors; Bulk heterojunction organic solar cells; Power conversion efficiency; Solvent additives; Small molecules; Solution process
Citation
DYES AND PIGMENTS, v.120, pp.126 - 135
Indexed
SCIE
SCOPUS
Journal Title
DYES AND PIGMENTS
Volume
120
Start Page
126
End Page
135
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/92594
DOI
10.1016/j.dyepig.2015.04.012
ISSN
0143-7208
Abstract
The synthesis and characterization of two D-A-D-A-D push-pull organic semiconductors based on either his- (2-ethylhexyloxy) benzo [1,2-b:4,5-b'] dithiophene or bis- (triisopropylsilylethynyl) benzodithiophene electron rich core are described. The optical and electrochemical properties of these compounds indicate that these materials can absorb sunlight over a wide spectral range from 350 to 700 nm and exhibit suitable energy levels for efficient exciton dissociation. These small molecules were used as donor coupled with phenyl-C-71-butyric acid methyl ester acceptor for the fabrication of solution processed small molecule bulk heterojunction solar cells. The rigid and -conjugation of the silylacetylene substituted analog pi-extended compared to the hexyloxy substituted analog facilitates intermolecular packing interactions of small pi-pi charge transfer and intermolecular molecule which induce a deep HOMO level, producing a high open circuit voltage of similar to 0.98 V. The achieved PCE was 5.69% when the active layer hexyloxy analog: phenyl-C-71-butyric acid methyl ester was processed with optimized 1-chloronaphathalene additive. (C) 2015 Elsevier Ltd. All rights reserved.
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