Issue 38, 2014

Air-stable organic semiconductors based on 6,6′-dithienylindigo and polymers thereof

Abstract

Herein we report on the synthesis and properties of 6,6′-dithienylindigo (DTI), as well as its solubilized N,N′-di(tert-butoxy carbonyl) derivative (tBOC-DTI). tBOC-DTI can be electropolymerized and thermally interconverted into films of poly(DTI). Thin films of DTI afford quasi-reversible 2-electron reduction and oxidation electrochemistry, and demonstrate ambipolar charge transport in organic field-effect transistors with a hole mobility of up to 0.11 cm2 V−1 s−1 and an electron mobility of up to 0.08 cm2 V−1 s−1. Operation of the p-channel shows excellent air stability, with minimal degradation over a 60 day stressing study. Poly(DTI) can be reversibly oxidized and reduced over hundreds of cycles while remaining immobilized on the working electrode surface, and additionally shows a pronounced photoconductivity response in a diode device geometry. This work shows the potential of extended indigo derivatives for organic electronic applications, demonstrating impressive stability under ambient conditions.

Graphical abstract: Air-stable organic semiconductors based on 6,6′-dithienylindigo and polymers thereof

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2014
Accepted
21 Jul 2014
First published
22 Jul 2014

J. Mater. Chem. C, 2014,2, 8089-8097

Author version available

Air-stable organic semiconductors based on 6,6′-dithienylindigo and polymers thereof

E. D. Głowacki, D. H. Apaydin, Z. Bozkurt, U. Monkowius, K. Demirak, E. Tordin, M. Himmelsbach, C. Schwarzinger, M. Burian, R. T. Lechner, N. Demitri, G. Voss and N. S. Sariciftci, J. Mater. Chem. C, 2014, 2, 8089 DOI: 10.1039/C4TC00651H

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