Detail publikace
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
Originální název
Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells
Typ
článek v časopise ve Web of Science, Jimp
Jazyk
angličtina
Originální abstrakt
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.
Klíčová slova
organic solar cell, thiophene-free, diphenyl-amino-stilbene, hole mobility, molecular structure
Autoři
Jana Honová, Stanislav Luňák, Martin Vala, Stanislav Střítesk ́y, Ladislav Fekete, Martin Weiter, Alexander Kovalenko
Vydáno
26. 5. 2016
Nakladatel
DE GRUYTER
Místo
Germany, Berlin
ISSN
1336-9075
Periodikum
Chemical Papers
Ročník
1
Číslo
1
Stát
Slovenská republika
Strany od
1
Strany do
9
Strany počet
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"
}