4.5 Article

Organic electronic applications and charge transport mechanism in novel discotic liquid crystals

Journal

LIQUID CRYSTALS
Volume -, Issue -, Pages -

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/02678292.2023.2188616

Keywords

Discotic liquid crystal; charge transport; charge carrier mobility; time-of-flight technique

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This article presents the charge transport and organic electronic applications of naphthophenanthridine derivatives and a dimer composed of pentaalkynylbenzene and triphenylene discotic liquid crystals. The investigated compounds exhibit high ambipolar charge carrier mobility, making them suitable for fabricating organic semiconducting electronic devices.
Triphenylene-based pentaalkynylbenzene dyads and naphthophenanthridine derivativediscotic mesogens have been proven a backbone-like utility for modern optoelectronic applications. Herein, we present the charge transport and organic electronic applications of naphthophenanthridine derivatives and a dimer composed of pentaalkynylbenzene (PA) and triphenylene (TP) discotic liquid crystals (DLCs). Naphthophenanthridine derivatives exhibit a hexagonal columnar (Col(h)) phase; whereas, triphenylene-pentaalkynylbenzene dyads show a columnar centred rectangular (Col(r)) phase and transform into Col(h) phase on doping the pure compounds with an electron-acceptor 2,4,7-trinitrofluorenone (TNF) in a 2:1 TNF/compound ratio. The ambipolar charge transport behaviour of the compounds mentioned above has been investigated by the time-of-flight technique. Naphthophenanthridine derivative renders an ambipolar charge transport, showing temperature-independent electron and hole mobility of the order of 3 x 10(-4) cm(2)/Vs; whereas, TP-PA dimer yields an ambipolar charge carrier mobility of order 10(-3) cm(2)/Vs. The phenazine-fused triphenylene DLC shows unipolar hole mobility of the order of 10(-4) cm(2)/Vs; whereas, hydrogen-bonded Hpz-C-9-TP DLCs exhibit ambipolar charge mobility of the order of 10(-2) cm(2)/Vs. The high ambipolar charge carrier mobility in the investigated DLC compounds makes them suitable for fabricating organic semiconducting electronic devices.

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