Cargando…

Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application

Two kinds of donor–acceptor π-conjugated copolymer based on poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[isoindigo]} (PDTP-IID) and poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[thiazol-2,5-diyl]} (PDTP-Thz) were investigated. These copolymers were synthesized via a Stille...

Descripción completa

Detalles Bibliográficos
Autores principales: Trinh, Cuc Kim, Nassar, Gamal M., Abdo, Nabiha I., Jung, Suhyun, Kim, Wonbin, Lee, Kwanghee, Lee, Jae-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198993/
https://www.ncbi.nlm.nih.gov/pubmed/35765342
http://dx.doi.org/10.1039/d2ra02608b
_version_ 1784727765965078528
author Trinh, Cuc Kim
Nassar, Gamal M.
Abdo, Nabiha I.
Jung, Suhyun
Kim, Wonbin
Lee, Kwanghee
Lee, Jae-Suk
author_facet Trinh, Cuc Kim
Nassar, Gamal M.
Abdo, Nabiha I.
Jung, Suhyun
Kim, Wonbin
Lee, Kwanghee
Lee, Jae-Suk
author_sort Trinh, Cuc Kim
collection PubMed
description Two kinds of donor–acceptor π-conjugated copolymer based on poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[isoindigo]} (PDTP-IID) and poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[thiazol-2,5-diyl]} (PDTP-Thz) were investigated. These copolymers were synthesized via a Stille coupling reaction. The results showed the structure–property relationships of different donor–acceptor (D–A) combinations. The polymer structures and photophysical properties were characterized by (1)H NMR, TGA, DSC, UV-vis absorption spectroscopy, AFM, CV, and XRD measurement. Through UV-vis absorption and cyclic voltammetry (CV) measurements, it showed that the copolymers exhibit not only a low bandgap of 1.29 eV and 1.51 eV but also a deep highest occupied molecular orbital (HOMO) of −5.49 and −5.11 eV. Moreover, photovoltaic properties in combination with the fullerene derivatives were investigated. The device based on the copolymers with PC(71)BM exhibited higher maximum power conversion efficiency and higher maximum short-circuit current density of 0.23% with 1.64 mA cm(−2) of PDTP-IID:PC(71)BM and 0.13% with 1.11 mA cm(−2) of PDTP-Thz:PC(71)BM than those of the copolymers with PC(61)BM. Measurements performed for N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-based copolymers proved the potential of these polymers to be applied in optoelectronic applications.
format Online
Article
Text
id pubmed-9198993
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-91989932022-06-27 Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application Trinh, Cuc Kim Nassar, Gamal M. Abdo, Nabiha I. Jung, Suhyun Kim, Wonbin Lee, Kwanghee Lee, Jae-Suk RSC Adv Chemistry Two kinds of donor–acceptor π-conjugated copolymer based on poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[isoindigo]} (PDTP-IID) and poly{[N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-2,6-diyl]alt-[thiazol-2,5-diyl]} (PDTP-Thz) were investigated. These copolymers were synthesized via a Stille coupling reaction. The results showed the structure–property relationships of different donor–acceptor (D–A) combinations. The polymer structures and photophysical properties were characterized by (1)H NMR, TGA, DSC, UV-vis absorption spectroscopy, AFM, CV, and XRD measurement. Through UV-vis absorption and cyclic voltammetry (CV) measurements, it showed that the copolymers exhibit not only a low bandgap of 1.29 eV and 1.51 eV but also a deep highest occupied molecular orbital (HOMO) of −5.49 and −5.11 eV. Moreover, photovoltaic properties in combination with the fullerene derivatives were investigated. The device based on the copolymers with PC(71)BM exhibited higher maximum power conversion efficiency and higher maximum short-circuit current density of 0.23% with 1.64 mA cm(−2) of PDTP-IID:PC(71)BM and 0.13% with 1.11 mA cm(−2) of PDTP-Thz:PC(71)BM than those of the copolymers with PC(61)BM. Measurements performed for N-hexyl-dithieno(3,2-b:2′,3′-d)pyrrole-based copolymers proved the potential of these polymers to be applied in optoelectronic applications. The Royal Society of Chemistry 2022-06-15 /pmc/articles/PMC9198993/ /pubmed/35765342 http://dx.doi.org/10.1039/d2ra02608b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Trinh, Cuc Kim
Nassar, Gamal M.
Abdo, Nabiha I.
Jung, Suhyun
Kim, Wonbin
Lee, Kwanghee
Lee, Jae-Suk
Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title_full Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title_fullStr Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title_full_unstemmed Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title_short Synthesis and photophysical properties of N-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
title_sort synthesis and photophysical properties of n-alkyl dithieno[3,2-b:2′,3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198993/
https://www.ncbi.nlm.nih.gov/pubmed/35765342
http://dx.doi.org/10.1039/d2ra02608b
work_keys_str_mv AT trinhcuckim synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT nassargamalm synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT abdonabihai synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT jungsuhyun synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT kimwonbin synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT leekwanghee synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication
AT leejaesuk synthesisandphotophysicalpropertiesofnalkyldithieno32b23dpyrrolebaseddonoracceptorpconjugatedcopolymersforsolarcellapplication