Detail publikačního výsledku
Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials
Alexander Kovalenko, Cigdem Yumusak, Patricie Heinrichova, Stanislav Stritesky, Ladislav Fekete, Martin Vala, Martin Weiter, Niyazi Serdar Sariciftci and Jozef Krajcovic
Originální název
Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials
Anglický název
Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials
Druh
Článek WoS
Originální abstrakt
Novel ethyladamantylsolubilization side groups were found to induce pi-pi interactions between the conjugated cores through adamantyl–adamantyl stacking in soluble diketopyrrolopyrrole (DPP) derivatives. The closeness of the DPP cores amplifies charge transfer in the material,as far as pi-pi interaction is a dominant charge-hopping pathway. As a result, tenfold enhancement of hole mobilities exceeding those obtained for insoluble derivativeswasreached. Moreover, due to high crystallinity and co-planarity of the conjugated cores, electron transfer was preserved with a mobility of 0.2 cm2/(Vs)for dithiophene-DPP. At the same time, the material remained soluble, which is a significant advantage for purification and processing. This approach can be universally applied for many types of semiconducting organic materials containingtheimide motive, where solubilization is achieved by side-group substitution. Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials.
Anglický abstrakt
Novel ethyladamantylsolubilization side groups were found to induce pi-pi interactions between the conjugated cores through adamantyl–adamantyl stacking in soluble diketopyrrolopyrrole (DPP) derivatives. The closeness of the DPP cores amplifies charge transfer in the material,as far as pi-pi interaction is a dominant charge-hopping pathway. As a result, tenfold enhancement of hole mobilities exceeding those obtained for insoluble derivativeswasreached. Moreover, due to high crystallinity and co-planarity of the conjugated cores, electron transfer was preserved with a mobility of 0.2 cm2/(Vs)for dithiophene-DPP. At the same time, the material remained soluble, which is a significant advantage for purification and processing. This approach can be universally applied for many types of semiconducting organic materials containingtheimide motive, where solubilization is achieved by side-group substitution. Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials.
Klíčová slova
diketopyrrolopyrrole, side-chain engineering, OFET, ambipolarity, field-effectmobility
Klíčová slova v angličtině
diketopyrrolopyrrole, side-chain engineering, OFET, ambipolarity, field-effectmobility
Autoři
Alexander Kovalenko, Cigdem Yumusak, Patricie Heinrichova, Stanislav Stritesky, Ladislav Fekete, Martin Vala, Martin Weiter, Niyazi Serdar Sariciftci and Jozef Krajcovic
Rok RIV
2018
Vydáno
13.04.2017
ISSN
2050-7534
Periodikum
Journal of Materials Chemistry C
Svazek
5
Číslo
19
Stát
Spojené království Velké Británie a Severního Irska
Strany od
1
Strany do
10
Strany počet
10
URL
BibTex
@article{BUT135191,
  author="Alexander {Kovalenko} and Patricie {Heinrichová} and Stanislav {Stříteský} and Martin {Vala} and Martin {Weiter} and Jozef {Krajčovič}",
  title="Adamantane substitutions: a path to high-performing, soluble, versatile and sustainable organic semiconducting materials",
  journal="Journal of Materials Chemistry C",
  year="2017",
  volume="5",
  number="19",
  pages="1--10",
  doi="10.1039/C6TC05076J",
  issn="2050-7526",
  url="https://pubs.rsc.org/en/content/articlelanding/2017/tc/c6tc05076j#!divAbstract"
}Dokumenty