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Oxadiazole-integrated heterocoronene discotics as ambipolar organic semiconductors
The development of modern technologies has driven a quest for new semiconducting materials in optoelectronics, where self-assembled liquid crystal (LC) materials can play a potential role. The molecular engineering of disc-shaped LCs (DLCs) with suitable organic moieties, especially heterocyclic uni...
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Published in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2023-01, Vol.11 (3), p.98-985 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The development of modern technologies has driven a quest for new semiconducting materials in optoelectronics, where self-assembled liquid crystal (LC) materials can play a potential role. The molecular engineering of disc-shaped LCs (DLCs) with suitable organic moieties, especially heterocyclic units, can lead to control over their columnar architecture in the nano-scale regime, which holds the key to tuning the charge-transport properties of the system. Here, we have successfully designed and synthesized room-temperature DLCs (
1.1
,
1.2
and
1.3
) with 1,3,4-oxadiazole functional units acting as electron-deficient linkers between a central heterocoronene core and the peripheral alkoxy phenyl units. All the derivatives exhibited a broad columnar hexagonal mesophase range with high isotropic temperatures. When employed in space-charge limited current (SCLC) devices, they showed ambipolar charge transport behaviour in thin films, with maximum hole and electron mobilities of the order of 10
−3
and 10
−5
cm
2
V
−1
s
−1
, respectively.
Disc-shaped liquid crystals designed by introducing oxadiazole functional units into a heterocoronene system were explored in thin-film space-charge limited current (SCLC) devices. They were found to exhibit ambipolar semiconducting behavior. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d2tc04144h |