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Cyclopentadithiophene–benzothiadiazole oligomers: Synthesis via direct arylation, X-ray crystallography, optical properties, solution casted field-effect transistor and photovoltaic characteristics

Chang, S-W. and Waters, H. and Kettle, J. and Horie, M. (2012) Cyclopentadithiophene–benzothiadiazole oligomers: Synthesis via direct arylation, X-ray crystallography, optical properties, solution casted field-effect transistor and photovoltaic characteristics. Organic Electronics, 13 ((12)). pp. 2967-2974. DOI: 10.1016/j.orgel.2012.08.023

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Abstract

This article reports the synthesis, crystallographic structure and OFET and OPV performance of the conjugated oligomer of cyclopentadithiophene (CPDT) with benzothiadiazole (BT). Synthesis of the oligomer composed of the CPDT-BT-CPDT sequence is accomplished using direct arylation reactions. Theoretical and experimental X-ray single crystallography confirms that two CPDT-BT-CPDT molecules are not entirely disordered, but are actually stacking directly across each other at the central BT units with an intermolecular distance of 3.61 �, providing valuable insight into the polymer bulk structure. The performance of the oligomer in OFET devices is investigated by fabricating bottom gate top contact devices and demonstrates a hole mobility of 5.0 � 10�3 cm2 V�1 s�1. OPV devices of the oligomer blended with PC61BM and PC71BM show power conversion efficiency (PCE) of 1.61%. One potential use for the oligomer could be as a sensitiser in a ternary blend with P3HT�PC61BM or PCPDTBT�PC61BM OPVs; the PCE can be relatively increased by 3�9% depending on concentration, primarily as a result of increased short circuit current density.

Item Type: Article
Subjects: Research Publications
Departments: College of Physical and Applied Sciences > School of Electronic Engineering
Date Deposited: 09 Dec 2014 16:47
Last Modified: 23 Sep 2015 03:10
ISSN: 1566-1199
URI: http://e.bangor.ac.uk/id/eprint/1092
Identification Number: DOI: 10.1016/j.orgel.2012.08.023
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