Cargando…
An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application
A new phenacene-type molecule, [8]phenacene, which is an extended zigzag chain of coplanar fused benzene rings, has been synthesised for use in an organic field-effect transistor (FET). The molecule consists of a phenacene core of eight benzene rings, which has a lengthy π-conjugated system. The str...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060465/ https://www.ncbi.nlm.nih.gov/pubmed/24936854 http://dx.doi.org/10.1038/srep05330 |
_version_ | 1782321376949960704 |
---|---|
author | Okamoto, Hideki Eguchi, Ritsuko Hamao, Shino Goto, Hidenori Gotoh, Kazuma Sakai, Yusuke Izumi, Masanari Takaguchi, Yutaka Gohda, Shin Kubozono, Yoshihiro |
author_facet | Okamoto, Hideki Eguchi, Ritsuko Hamao, Shino Goto, Hidenori Gotoh, Kazuma Sakai, Yusuke Izumi, Masanari Takaguchi, Yutaka Gohda, Shin Kubozono, Yoshihiro |
author_sort | Okamoto, Hideki |
collection | PubMed |
description | A new phenacene-type molecule, [8]phenacene, which is an extended zigzag chain of coplanar fused benzene rings, has been synthesised for use in an organic field-effect transistor (FET). The molecule consists of a phenacene core of eight benzene rings, which has a lengthy π-conjugated system. The structure was verified by elemental analysis, solid-state NMR, X-ray diffraction (XRD) pattern, absorption spectrum and photoelectron yield spectroscopy (PYS). This type of molecule is quite interesting, not only as pure chemistry but also for its potential electronics applications. Here we report the physical properties of [8]phenacene and its FET application. An [8]phenacene thin-film FET fabricated with an SiO(2) gate dielectric showed clear p-channel characteristics. The highest μ achieved in an [8]phenacene thin-film FET with an SiO(2) gate dielectric is 1.74 cm(2) V(−1) s(−1), demonstrating excellent FET characteristics; the average μ was evaluated as 1.2(3) cm(2) V(−1) s(−1). The μ value in the [8]phenacene electric-double-layer FET reached 16.4 cm(2) V(−1) s(−1), which is the highest reported in EDL FETs based on phenacene-type molecules; the average μ was evaluated as 8(5) cm(2) V(−1) s(−1). The μ values recorded in this study show that [8]phenacene is a promising molecule for transistor applications. |
format | Online Article Text |
id | pubmed-4060465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40604652014-06-18 An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application Okamoto, Hideki Eguchi, Ritsuko Hamao, Shino Goto, Hidenori Gotoh, Kazuma Sakai, Yusuke Izumi, Masanari Takaguchi, Yutaka Gohda, Shin Kubozono, Yoshihiro Sci Rep Article A new phenacene-type molecule, [8]phenacene, which is an extended zigzag chain of coplanar fused benzene rings, has been synthesised for use in an organic field-effect transistor (FET). The molecule consists of a phenacene core of eight benzene rings, which has a lengthy π-conjugated system. The structure was verified by elemental analysis, solid-state NMR, X-ray diffraction (XRD) pattern, absorption spectrum and photoelectron yield spectroscopy (PYS). This type of molecule is quite interesting, not only as pure chemistry but also for its potential electronics applications. Here we report the physical properties of [8]phenacene and its FET application. An [8]phenacene thin-film FET fabricated with an SiO(2) gate dielectric showed clear p-channel characteristics. The highest μ achieved in an [8]phenacene thin-film FET with an SiO(2) gate dielectric is 1.74 cm(2) V(−1) s(−1), demonstrating excellent FET characteristics; the average μ was evaluated as 1.2(3) cm(2) V(−1) s(−1). The μ value in the [8]phenacene electric-double-layer FET reached 16.4 cm(2) V(−1) s(−1), which is the highest reported in EDL FETs based on phenacene-type molecules; the average μ was evaluated as 8(5) cm(2) V(−1) s(−1). The μ values recorded in this study show that [8]phenacene is a promising molecule for transistor applications. Nature Publishing Group 2014-06-17 /pmc/articles/PMC4060465/ /pubmed/24936854 http://dx.doi.org/10.1038/srep05330 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Okamoto, Hideki Eguchi, Ritsuko Hamao, Shino Goto, Hidenori Gotoh, Kazuma Sakai, Yusuke Izumi, Masanari Takaguchi, Yutaka Gohda, Shin Kubozono, Yoshihiro An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title | An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title_full | An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title_fullStr | An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title_full_unstemmed | An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title_short | An Extended Phenacene-type Molecule, [8]Phenacene: Synthesis and Transistor Application |
title_sort | extended phenacene-type molecule, [8]phenacene: synthesis and transistor application |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060465/ https://www.ncbi.nlm.nih.gov/pubmed/24936854 http://dx.doi.org/10.1038/srep05330 |
work_keys_str_mv | AT okamotohideki anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT eguchiritsuko anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT hamaoshino anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gotohidenori anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gotohkazuma anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT sakaiyusuke anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT izumimasanari anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT takaguchiyutaka anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gohdashin anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT kubozonoyoshihiro anextendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT okamotohideki extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT eguchiritsuko extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT hamaoshino extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gotohidenori extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gotohkazuma extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT sakaiyusuke extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT izumimasanari extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT takaguchiyutaka extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT gohdashin extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication AT kubozonoyoshihiro extendedphenacenetypemolecule8phenacenesynthesisandtransistorapplication |