Paper
17 November 2003 New liquid crystalline solution processible organic semiconductors and their performance in field effect transistors
Maxim N. Shkunov, Weimin Zhang, David Graham, David Sparrowe, Martin Heeney, Mark Giles, Steve Tierney, Clare Bailey, Iain McCulloch, Theo Kreouzis
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Abstract
New polymerisable liquid crystalline organic semiconductors based on small molecule "reactive mesogens" are reported. These molecules, comprising p-conjugated cores with reactive endgroups, were designed, synthesised then solution processed into thin films. The mesogenic morphology was attained thermally and fixed through a post fabrication photopolymerisation reaction. Thermal, optical and electrical properties of these thin films were characterised to reveal details of morphology and molecular orientation. Both bulk (time-of-flight) and surface (field-effect) charge carrier mobilities were measured. The relationship between molecular structure, corresponding macrostructure processability and charge mobility is discussed. Fabrication and characterisation of field-effect transistors based on reactive mesogens are presented and discussed.
© (2003) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Maxim N. Shkunov, Weimin Zhang, David Graham, David Sparrowe, Martin Heeney, Mark Giles, Steve Tierney, Clare Bailey, Iain McCulloch, and Theo Kreouzis "New liquid crystalline solution processible organic semiconductors and their performance in field effect transistors", Proc. SPIE 5217, Organic Field Effect Transistors II, (17 November 2003); https://doi.org/10.1117/12.505831
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Cited by 6 scholarly publications.
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KEYWORDS
Liquid crystals

Field effect transistors

Crystals

Liquids

Molecules

Transistors

Organic semiconductors

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