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Modification of alkyl side chain on thiophene-containing benzothieno[3,2-b]benzothiophene-based organic semiconductors for organic field-effect transistors

Authors
Kim, Y.Yun, C.Yun, S.Ho, D.Earmme, T.Kim, C.Seo, S.
Issue Date
1-Dec-2022
Publisher
Elsevier Ltd
Keywords
Organic field-effect transistors; Organic semiconductors; Side chain engineering; Solution-process; [1]benzothieno[3,2-b]benzothiophene
Citation
Synthetic Metals, v.291
Journal Title
Synthetic Metals
Volume
291
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/30392
DOI
10.1016/j.synthmet.2022.117173
ISSN
0379-6779
Abstract
In this study, three new organic semiconductors based on benzothieno[3,2-b]benzothiophene with double thiophene rings and different types of alkyl side chains were synthesized and characterized as active layers for organic field-effect transistors. Physicochemical properties of the newly synthesized organic compounds including thermal, optical, and electrochemical properties were characterized through thermogravimetric analysis (TGA), differential scanning calorimeter (DSC), UV–vis spectroscopy, and cyclic voltammetry (CV). The thin film surface morphology and texture of all three compounds fabricated by solution-shearing process were analyzed via atomic force microscopy (AFM) and θ-2θ X-ray diffraction (XRD). All semiconductor thin films showed p-channel activity and the compound with monoalkylated 2-ethylhexyl group as a substituent exhibited the highest electrical performance with carrier mobility of 0.033 cm2/Vs and current on/off ratio of ∼106. © 2022 Elsevier B.V.
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