Enabling high-mobility, ambipolar charge-transport in a DPP-benzotriazole copolymer by side-chain engineering. Issue 12 (8th September 2015)
- Record Type:
- Journal Article
- Title:
- Enabling high-mobility, ambipolar charge-transport in a DPP-benzotriazole copolymer by side-chain engineering. Issue 12 (8th September 2015)
- Main Title:
- Enabling high-mobility, ambipolar charge-transport in a DPP-benzotriazole copolymer by side-chain engineering
- Authors:
- Gruber, Mathias
Jung, Seok-Heon
Schott, Sam
Venkateshvaran, Deepak
Kronemeijer, Auke Jisk
Andreasen, Jens Wenzel
McNeill, Christopher R.
Wong, Wallace W. H.
Shahid, Munazza
Heeney, Martin
Lee, Jin-Kyun
Sirringhaus, Henning - Abstract:
- Abstract : In this article we discuss the synthesis of four new low band-gap co-polymers based on the diketopyrrolopyrrole (DPP) and benzotriazole (BTZ) monomer unit. Abstract : In this article we discuss the synthesis of four new low band-gap co-polymers based on the diketopyrrolopyrrole (DPP) and benzotriazole (BTZ) monomer unit. We demonstrate that the BTZ unit allows for additional solubilizing side-chains on the co-monomer and show that the introduction of a linear side-chain on the DPP-unit leads to an increase in thin-film order and charge-carrier mobility if a sufficiently solubilizing, branched, side chain is attached to the BTZ. We compare two different synthetic routes, direct arylation and Suzuki-polycondensation, by a direct comparison of polymers obtained via the two routes and show that direct arylation produces polymers with lower electrical performance which we attribute to a higher density of chain Furthermore we demonstrate that a polymer utilizing this design motif and synthesized via Suzuki-polycondensation ((l-C18 )-DPP-(b-C17 )-BTZ ) exhibits exceptionally high and near balanced average electron and hole mobilities >2 cm 2 V −1 s −1 which are among the highest, robustly extracted mobility values reported for DPP copolymers in a top-gate configuration to date. Our results demonstrate clearly that linear side chain substitution of the DPP unit together with co-monomers that allow for the use of sufficiently long or branched solubilizing side chains canAbstract : In this article we discuss the synthesis of four new low band-gap co-polymers based on the diketopyrrolopyrrole (DPP) and benzotriazole (BTZ) monomer unit. Abstract : In this article we discuss the synthesis of four new low band-gap co-polymers based on the diketopyrrolopyrrole (DPP) and benzotriazole (BTZ) monomer unit. We demonstrate that the BTZ unit allows for additional solubilizing side-chains on the co-monomer and show that the introduction of a linear side-chain on the DPP-unit leads to an increase in thin-film order and charge-carrier mobility if a sufficiently solubilizing, branched, side chain is attached to the BTZ. We compare two different synthetic routes, direct arylation and Suzuki-polycondensation, by a direct comparison of polymers obtained via the two routes and show that direct arylation produces polymers with lower electrical performance which we attribute to a higher density of chain Furthermore we demonstrate that a polymer utilizing this design motif and synthesized via Suzuki-polycondensation ((l-C18 )-DPP-(b-C17 )-BTZ ) exhibits exceptionally high and near balanced average electron and hole mobilities >2 cm 2 V −1 s −1 which are among the highest, robustly extracted mobility values reported for DPP copolymers in a top-gate configuration to date. Our results demonstrate clearly that linear side chain substitution of the DPP unit together with co-monomers that allow for the use of sufficiently long or branched solubilizing side chains can be an attractive design motif for solution processable, high mobility DPP copolymers. … (more)
- Is Part Of:
- Chemical science. Volume 6:Issue 12(2015:Dec.)
- Journal:
- Chemical science
- Issue:
- Volume 6:Issue 12(2015:Dec.)
- Issue Display:
- Volume 6, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 6
- Issue:
- 12
- Issue Sort Value:
- 2015-0006-0012-0000
- Page Start:
- 6949
- Page End:
- 6960
- Publication Date:
- 2015-09-08
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5sc01326g ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9.xml