Issue 47, 2012

Novel triethylsilylethynyl anthracene-based organic semiconductors for high performance field effect transistors

Abstract

A series of triethylsilylethynyl anthracene (TESAN) derivatives, end-capped with bithiophene and thienothiophene, were synthesized by Suzuki coupling. The thermal, optical, electrochemical, and crystalline properties of the TESAN derivatives were reported and correlated with charge transport behavior measured via both a thin film transistor and a single crystal transistor. The TESAN derivative substituted with bithiophene exhibited more efficient π electron delocalization over the molecule compared to the derivative substituted with fused thienothiophene, and consequently gave the highest FET mobility, 1.28 cm2 V−1 s−1, from single crystal transistors with negligible hysteresis and almost zero turn-on voltage. The discrepancy of charge carrier mobility between the thin film transistor and single crystal transistor and the solvent annealing effects are discussed in conjunction with morphological and structural analyses.

Graphical abstract: Novel triethylsilylethynyl anthracene-based organic semiconductors for high performance field effect transistors

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2012
Accepted
01 Oct 2012
First published
01 Oct 2012

J. Mater. Chem., 2012,22, 24924-24929

Novel triethylsilylethynyl anthracene-based organic semiconductors for high performance field effect transistors

H. Yun, D. S. Chung, I. Kang, J. W. Park, Y. Kim and S. Kwon, J. Mater. Chem., 2012, 22, 24924 DOI: 10.1039/C2JM34160C

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