Issue 9, 2008

Functionalized anthradithiophenes for organic field-effect transistors

Abstract

Two new semiconductors for organic thin-film transistors (OTFTs), diperfluorophenyl anthradithiophene (DFPADT) and dimethyl anthradithiophene (DMADT), have been synthesized and characterized. The first material exhibits ambipolar transport in OTFT devices with field-effect mobilities (μ) of 6 × 10−4 cm2 V−1 s−1 and 0.05 cm2 V−1 s−1 for electrons and holes, respectively. Therefore, diperfluorophenyl substitution was found to be effective to induce n-type transport. Dimethyl-substituted anthradithiophene (DMADT) was also synthesized for comparison and exhibited exclusively hole transport with carrier mobility of ∼0.1 cm2 V−1 s−1. Within this semiconductor family, OTFT carrier mobility values are strongly dependent on the semiconductor film growth conditions, substrate deposition temperatures, and gate dielectric surface treatment.

Graphical abstract: Functionalized anthradithiophenes for organic field-effect transistors

Supplementary files

Article information

Article type
Paper
Submitted
11 Oct 2007
Accepted
03 Jan 2008
First published
25 Jan 2008

J. Mater. Chem., 2008,18, 1029-1036

Functionalized anthradithiophenes for organic field-effect transistors

M. Chen, C. Kim, S. Chen, Y. Chiang, M. Chung, A. Facchetti and T. J. Marks, J. Mater. Chem., 2008, 18, 1029 DOI: 10.1039/B715746K

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