Cargando…
Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells
ABSTRACT: Herein, we describe the synthesis and characterization of a conjugated donor–acceptor copolymer consisting of a pyrrolopyridazinedione (PPD) acceptor unit, and a benzodithiophene (BDT) donor unit. The polymerization was done via a Stille cross-coupling polycondensation. The resulting PPD–B...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387020/ https://www.ncbi.nlm.nih.gov/pubmed/28458400 http://dx.doi.org/10.1007/s00706-017-1949-1 |
_version_ | 1782520860845801472 |
---|---|
author | Knall, Astrid-Caroline Jones, Andrew O. F. Kunert, Birgit Resel, Roland Reishofer, David Zach, Peter W. Kirkus, Mindaugas McCulloch, Iain Rath, Thomas |
author_facet | Knall, Astrid-Caroline Jones, Andrew O. F. Kunert, Birgit Resel, Roland Reishofer, David Zach, Peter W. Kirkus, Mindaugas McCulloch, Iain Rath, Thomas |
author_sort | Knall, Astrid-Caroline |
collection | PubMed |
description | ABSTRACT: Herein, we describe the synthesis and characterization of a conjugated donor–acceptor copolymer consisting of a pyrrolopyridazinedione (PPD) acceptor unit, and a benzodithiophene (BDT) donor unit. The polymerization was done via a Stille cross-coupling polycondensation. The resulting PPD–BDT copolymer revealed an optical bandgap of 1.8 eV and good processability from chlorobenzene solutions. In an organic solar cell in combination with PC(70)BM, the polymer led to a power conversion efficiency of 4.5%. Moreover, the performance of the copolymer was evaluated in polymer/nanocrystal hybrid solar cells using non-toxic CuInS(2) nanocrystals as inorganic phase, which were prepared from precursors directly in the polymer matrix without using additional capping ligands. The PPD–BDT/CuInS(2) hybrid solar cells showed comparably high photovoltages and a power conversion efficiency of 2.2%. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-5387020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-53870202017-04-27 Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells Knall, Astrid-Caroline Jones, Andrew O. F. Kunert, Birgit Resel, Roland Reishofer, David Zach, Peter W. Kirkus, Mindaugas McCulloch, Iain Rath, Thomas Monatsh Chem Original Paper ABSTRACT: Herein, we describe the synthesis and characterization of a conjugated donor–acceptor copolymer consisting of a pyrrolopyridazinedione (PPD) acceptor unit, and a benzodithiophene (BDT) donor unit. The polymerization was done via a Stille cross-coupling polycondensation. The resulting PPD–BDT copolymer revealed an optical bandgap of 1.8 eV and good processability from chlorobenzene solutions. In an organic solar cell in combination with PC(70)BM, the polymer led to a power conversion efficiency of 4.5%. Moreover, the performance of the copolymer was evaluated in polymer/nanocrystal hybrid solar cells using non-toxic CuInS(2) nanocrystals as inorganic phase, which were prepared from precursors directly in the polymer matrix without using additional capping ligands. The PPD–BDT/CuInS(2) hybrid solar cells showed comparably high photovoltages and a power conversion efficiency of 2.2%. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2017-03-30 2017 /pmc/articles/PMC5387020/ /pubmed/28458400 http://dx.doi.org/10.1007/s00706-017-1949-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Knall, Astrid-Caroline Jones, Andrew O. F. Kunert, Birgit Resel, Roland Reishofer, David Zach, Peter W. Kirkus, Mindaugas McCulloch, Iain Rath, Thomas Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title | Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title_full | Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title_fullStr | Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title_full_unstemmed | Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title_short | Synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (PPD–BDT) copolymer and its application in organic and hybrid solar cells |
title_sort | synthesis of a conjugated pyrrolopyridazinedione–benzodithiophene (ppd–bdt) copolymer and its application in organic and hybrid solar cells |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387020/ https://www.ncbi.nlm.nih.gov/pubmed/28458400 http://dx.doi.org/10.1007/s00706-017-1949-1 |
work_keys_str_mv | AT knallastridcaroline synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT jonesandrewof synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT kunertbirgit synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT reselroland synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT reishoferdavid synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT zachpeterw synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT kirkusmindaugas synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT mccullochiain synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells AT raththomas synthesisofaconjugatedpyrrolopyridazinedionebenzodithiopheneppdbdtcopolymeranditsapplicationinorganicandhybridsolarcells |