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Issue 47, 2014
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Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processing

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Abstract

To understand and optimize the performance of thin-film electronic devices incorporating crystalline organic semiconductors, it is important to consider the impact of their structural anisotropy on the charge transport. Here we report on the charge mobility anisotropy in 6,13-bis(triisopropylsilylethynyl) (TIPS) and 6,13-bis(triethylsilylethynyl) (TES) pentacene field effect transistors, in which microstructure is controlled by solution processing conditions. Thin-film structures that range from millimetre size, crystalline domains to macroscopic, high-aspect-ratio (∼1 μm wide and >1 cm long) needles are systematically produced by controlling the substrate displacement rate during zone-cast deposition. Through precise control of the microstructure we experimentally explore the differences in charge transport anisotropy between TIPS- and TES-pentacene molecules. Aligned needles of TIPS- pentacene result in a mobility anisotropy (μ/μ) of ∼20 (mobility of ∼0.7 cm2 V−1 s−1) whereas TES-pentacene produce an order of magnitude lower mobility (∼0.06 cm2 V−1 s−1) but much higher mobility anisotropy (>45). Such significant changes in absolute mobility and mobility anisotropy are attributed to their different packing structures, which permit 2D charge transport in TIPS-pentacene and 1D transport in TES-pentacene. Bulky TIPS- side groups (diameter ∼7.5 Å) force a brick-wall type packing structure, whereas TES- side groups (diameter ∼6.6 Å) pack in a 1D slipped-stack. Furthermore, through precise control of the molecular alignment, the impact of crystal orientation on charge transport is investigated. TIPS-pentacene achieves the highest mobility when the angle between the needle long-axis and charge transport directions is ∼35°, whereas in TES-pentacene it is much closer to 0°. These results are supported by theoretical simulations.

Graphical abstract: Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processing

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Publication details

The article was received on 24 Jun 2014, accepted on 26 Sep 2014 and first published on 20 Oct 2014


Article type: Paper
DOI: 10.1039/C4TC01353K
Citation: J. Mater. Chem. C, 2014,2, 10110-10115

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    Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processing

    J. Wade, F. Steiner, D. Niedzialek, D. T. James, Y. Jung, D. Yun, D. D. C. Bradley, J. Nelson and J. Kim, J. Mater. Chem. C, 2014, 2, 10110
    DOI: 10.1039/C4TC01353K

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