Publication detail
Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells
Jana Honová, Stanislav Luňák, Martin Vala, Stanislav Střítesk ́y, Ladislav Fekete, Martin Weiter, Alexander Kovalenko
Original Title
Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells
Type
journal article in Web of Science
Language
English
Original Abstract
An extended study on a group of four soluble diphenyl-amino-stilbene based diphenyl-diketopyrrolo-pyrrole molecules has been carried out. Using the materials in thin-film transistors it was shown that the above-mentioned compounds can be successfully used as donors in organic photovoltaic devices. Influence of the molecular symmetry and solubilizing chain on the morphology and solar cell performance are described. It was shown that a shorter and non-branched ethyl acetate chain leads to higher charge carrier mobility, short circuit current, and better fill factor. After the basic optimization, a power conversion efficiency of about 1.5 % was reached. This, to the best of our knowledge, is the highest reported efficiency of thiophene-free small-molecule diketo-pyrrolopyrroles.
Keywords
organic solar cell, thiophene-free, diphenyl-amino-stilbene, hole mobility, molecular structure
Authors
Jana Honová, Stanislav Luňák, Martin Vala, Stanislav Střítesk ́y, Ladislav Fekete, Martin Weiter, Alexander Kovalenko
Released
26. 5. 2016
Publisher
DE GRUYTER
Location
Germany, Berlin
ISBN
1336-9075
Periodical
Chemical Papers
Year of study
1
Number
1
State
Slovak Republic
Pages from
1
Pages to
9
Pages count
9
URL
BibTex
@article{BUT126481,
author="Alexander {Kovalenko} and Jana {Vrchotová} and Stanislav {Luňák} and Martin {Vala} and Stanislav {Stříteský} and Martin {Weiter}",
title="Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells",
journal="Chemical Papers",
year="2016",
volume="1",
number="1",
pages="1--9",
doi="10.1515/chempap-2016-0068",
issn="1336-9075",
url="https://www.degruyter.com/dg/journalprintahead.articlelist.resultlinks.fullcontentlink:pdfeventlink/$002fj$002fchempap.ahead-of-print$002fchempap-2016-0068$002fchempap-2016-0068.pdf/chempap-2016-0068.pdf?t:ac=j$002fchempap"
}