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Crystalline nanostructure and morphology of TriF-IF-dione for high-performance stable n-type field-effect transistors

Authors
Kim, Beom JoonPark, Young-IlKim, Hyo JungAhn, KwangseokLee, Dong RyeolKim, Do HwanOh, Se-YoungPark, Jong-WookCho, Jeong Ho
Issue Date
2012
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY, v.22, no.29, pp.14617 - 14623
Journal Title
JOURNAL OF MATERIALS CHEMISTRY
Volume
22
Number
29
Start Page
14617
End Page
14623
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/13487
DOI
10.1039/c2jm31698f
ISSN
0959-9428
Abstract
The device performance and stability of n-type organic field-effect transistors (OFETs) based on 1,2,3,7,8,9-hexafluoro-indeno[1,2-b]fluorene-6,12-dione (TriF-IF-dione) were investigated. The electrical characteristics of TriF-IF-dione FETs were optimized by systematically controlling the dielectric surface properties via insertion of organic interlayers, such as self-assembled monolayers (NH2-, CH3-, and CF3-) or polymeric layers (polystyrene, PS) at the semiconductor-SiO2 dielectric interfaces. In particular, a thin PS buffer layer on the SiO2 surface provided a device that performed well, with a field-effect mobility of 0.18 cm(2) V-1 s(-1) and an on-off current ratio of 4.4 x 10(6). The improvements in the performance of TriF-IF-dione OFET conveyed by the PS interlayers were examined in terms of the crystalline nanostructure and the charge modulation effects in the channel. These properties were strongly correlated with, respectively, the hydrophobicity and the electron-donating characteristics of the dielectric surface. The TriF-IF-dione FETs with a PS interlayer showed excellent electrical stability attributed to high activation energies for charge trap creation. A complementary inverter comprising both p-type pentacene and n-type TriF-IF-dione was also successfully demonstrated.
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