Issue 28, 2013

Oligofuran-containing molecules for organic electronics

Abstract

We describe the synthesis, characterization and field effect transistor (FET) properties of a series of furan-based conjugated oligomers such as unsubstituted, hexyl- and styryl-capped linear oligofurans and oligofuran-substituted anthracene derivatives. All studied oligofurans show high fluorescence and good thermal stability. Top contact organic FETs (OFETs) fabricated with oligofurans as the active layer show hole mobilities (∼0.01 to 0.07 cm2 V−1 s−1) and on/off ratios (104 to 106) on a par with the corresponding oligothiophene analogues, while the threshold voltages displayed by oligofuran-based OFETs are significantly reduced due to higher HOMO energies as compared to those of oligothiophenes. Electroluminescence observed in oligofuran-based OFETs in a bottom-contact geometry is limited by electron injection. Overall, we find that furan building blocks are excellent candidates for replacing thiophene in optoelectronic materials.

Graphical abstract: Oligofuran-containing molecules for organic electronics

Supplementary files

Article information

Article type
Paper
Submitted
13 Jan 2013
Accepted
21 Mar 2013
First published
26 Mar 2013

J. Mater. Chem. C, 2013,1, 4358-4367

Oligofuran-containing molecules for organic electronics

O. Gidron, A. Dadvand, E. Wei-Hsin Sun, I. Chung, L. J. W. Shimon, M. Bendikov and D. F. Perepichka, J. Mater. Chem. C, 2013, 1, 4358 DOI: 10.1039/C3TC00079F

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