Electronic transport properties of ensembles of perylene-substituted poly-isocyanopeptide arrays

Finlayson, Chris E., Friend, Richard H., Otten, Matthijs B. J., Schwartz, Erik, Cornelissen, Jeroen. J. L. M., Nolte, Roeland. L. M., Rowan, Alan E., Samori, Paolo, Palermo, Vicenzo, Liscio, Andrea, Peneva, Kalina, Muellen, Klaus, Trapani, Sara and Beljonne, David (2008) Electronic transport properties of ensembles of perylene-substituted poly-isocyanopeptide arrays. Advanced Functional Materials, 18 24: 3947-3955. doi:10.1002/adfm.200800943


Author Finlayson, Chris E.
Friend, Richard H.
Otten, Matthijs B. J.
Schwartz, Erik
Cornelissen, Jeroen. J. L. M.
Nolte, Roeland. L. M.
Rowan, Alan E.
Samori, Paolo
Palermo, Vicenzo
Liscio, Andrea
Peneva, Kalina
Muellen, Klaus
Trapani, Sara
Beljonne, David
Title Electronic transport properties of ensembles of perylene-substituted poly-isocyanopeptide arrays
Journal name Advanced Functional Materials   Check publisher's open access policy
ISSN 1616-301X
1616-3028
Publication date 2008-12-22
Year available 2008
Sub-type Article (original research)
DOI 10.1002/adfm.200800943
Open Access Status Not yet assessed
Volume 18
Issue 24
Start page 3947
End page 3955
Total pages 9
Place of publication Weinheim, Germany
Publisher Wiley - V C H Verlag GmbH & Co. KGaA
Language eng
Abstract The electronic transport properties of stacks of perylene- bis(dicarboximide) (PDI) chromophores, covalently fixed to the side arms of rigid, helical polyisocyanopeptides, are studied using thin-film transistors. In device architectures where the transistor channel lengths are somewhat greater than the average polymer chain length, carrier mobilities of order 10 -3 cm2 V-1 s-1 at 350K are found, which are limited by inter-chain transport processes. The influence of π-π interactions on the material properties is studied by using PDIs with and without bulky substituents in the bay area. In order to attain a deeper understanding of both the electronic and the electronic-transport properties of these systems, studies of self-assembly on surfaces are combined with electronic characterization using Kelvin probe force microscopy, and also a theoretical study of electronic coupling. The use of a rigid polymer backbone as a scaffold to achieve a full control over the position and orientation of functional groups is of general applicability and interest in the design of building blocks for technologically important functional materials, as well as in more fundamental studies of chromophoric interactions.
Keyword Chemistry, Multidisciplinary
Chemistry, Physical
Nanoscience & Nanotechnology
Materials Science, Multidisciplinary
Physics, Applied
Physics, Condensed Matter
Chemistry
Science & Technology - Other Topics
Materials Science
Physics
CHEMISTRY, MULTIDISCIPLINARY
CHEMISTRY, PHYSICAL
MATERIALS SCIENCE, MULTIDISCIPLINARY
NANOSCIENCE & NANOTECHNOLOGY
PHYSICS, APPLIED
PHYSICS, CONDENSED MATTER
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: Australian Institute for Bioengineering and Nanotechnology Publications
 
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