Organic field effect transistor characteristics of bis (styryl) anthracene analogues

Kenii Mochida; Misuzu Konishi; Katsuhiko Fujita; Tetsuo Tsutsui

Organic field effect transistor characteristics of bis (styryl) anthracene analogues

Kenii Mochida, Misuzu Konishi, Katsuhiko Fujita, Tetsuo Tsutsui

Department of Advanced Device Materials

Research output: Contribution to conference › Paper › peer-review

Abstract

Bisstyrylanthracene derivatives with long alkyl side chains(BSA) can give thin films composed of giant anisotropic domains by simple melt process. However the large ionization potential of (5.76eV) causes low carrier mobility due to the high hole injection barrier from Au electrode. We synthesized BSA analogues which have various heterocyclic substituents (Fig.2) to reduce barrier and fabricated organic FET devices by vacuum deposition (Fig.la). It has been found that BBTVA has smaller ionization potentials of 5.50eV and faster carrier mobility of 2.0 × 10^-5(cm²/Vs) than BSA.

Original language	English
Pages	1373
Number of pages	1
Publication status	Published - 2006
Event	55th SPSJ Annual Meeting - Nagoya, Japan Duration: May 24 2006 → May 26 2006

Other

Other	55th SPSJ Annual Meeting
Country/Territory	Japan
City	Nagoya
Period	5/24/06 → 5/26/06

All Science Journal Classification (ASJC) codes

Engineering(all)

Cite this

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title = "Organic field effect transistor characteristics of bis (styryl) anthracene analogues",

abstract = "Bisstyrylanthracene derivatives with long alkyl side chains(BSA) can give thin films composed of giant anisotropic domains by simple melt process. However the large ionization potential of (5.76eV) causes low carrier mobility due to the high hole injection barrier from Au electrode. We synthesized BSA analogues which have various heterocyclic substituents (Fig.2) to reduce barrier and fabricated organic FET devices by vacuum deposition (Fig.la). It has been found that BBTVA has smaller ionization potentials of 5.50eV and faster carrier mobility of 2.0 × 10-5(cm2/Vs) than BSA.",

author = "Kenii Mochida and Misuzu Konishi and Katsuhiko Fujita and Tetsuo Tsutsui",

year = "2006",

language = "English",

pages = "1373",

note = "55th SPSJ Annual Meeting ; Conference date: 24-05-2006 Through 26-05-2006",

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T1 - Organic field effect transistor characteristics of bis (styryl) anthracene analogues

AU - Mochida, Kenii

AU - Konishi, Misuzu

AU - Fujita, Katsuhiko

AU - Tsutsui, Tetsuo

PY - 2006

Y1 - 2006

N2 - Bisstyrylanthracene derivatives with long alkyl side chains(BSA) can give thin films composed of giant anisotropic domains by simple melt process. However the large ionization potential of (5.76eV) causes low carrier mobility due to the high hole injection barrier from Au electrode. We synthesized BSA analogues which have various heterocyclic substituents (Fig.2) to reduce barrier and fabricated organic FET devices by vacuum deposition (Fig.la). It has been found that BBTVA has smaller ionization potentials of 5.50eV and faster carrier mobility of 2.0 × 10-5(cm2/Vs) than BSA.

AB - Bisstyrylanthracene derivatives with long alkyl side chains(BSA) can give thin films composed of giant anisotropic domains by simple melt process. However the large ionization potential of (5.76eV) causes low carrier mobility due to the high hole injection barrier from Au electrode. We synthesized BSA analogues which have various heterocyclic substituents (Fig.2) to reduce barrier and fabricated organic FET devices by vacuum deposition (Fig.la). It has been found that BBTVA has smaller ionization potentials of 5.50eV and faster carrier mobility of 2.0 × 10-5(cm2/Vs) than BSA.

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M3 - Paper

AN - SCOPUS:33749853061

SP - 1373

T2 - 55th SPSJ Annual Meeting

Y2 - 24 May 2006 through 26 May 2006

ER -

Organic field effect transistor characteristics of bis (styryl) anthracene analogues

Abstract

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All Science Journal Classification (ASJC) codes

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