Detailed analysis and contact properties of low-voltage organic thin-film transistors based on dinaphtho[2,3-b2′,3′-f]thieno[3,2-b]thiophene (DNTT) and its didecyl and diphenyl derivatives.pdfVIP
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Detailed analysis and contact properties of low-voltage organic thin-film transistors based on dinaphtho[2,3-b2′,3′-f]thieno[3,2-b]thiophene (DNTT) and its didecyl and diphenyl derivatives.pdf
Organic Electronics 35 (2016) 33e40
Contents lists available at ScienceDirect
Organic Electronics
journal homepage: /locate/orgel
Detailed analysis and contact properties of low-voltage organic thin?lm transistors based on dinaphtho[2,3-b:20,30-f]thieno[3,2-b] thiophene (DNTT) and its didecyl and diphenyl derivatives
Ulrike Kraft a, b, *, Kazuo Takimiya c, Myeong Jin Kang d, Reinhold Ro€del a, Florian Letzkus e, Joachim N. Burghartz e, Edwin Weber b, Hagen Klauk a
a Max Planck Institute for Solid State Research, Stuttgart, Germany b Department of Chemistry, Technical University Bergakademie Freiberg, Germany c Emergent Molecular Function Research Group, RIKEN Center for Emergent Matter Science (CEMS), Wako, Saitama, Japan d Department of Applied Chemistry, Hiroshima University, Higashi-Hiroshima, Japan e Institute for Microelectronics/IMS Chips, Stuttgart, Germany
article info
Article history: Received 19 February 2016 Received in revised form 18 April 2016 Accepted 23 April 2016 Available online 12 May 2016
Keywords: Organic ?eld-effect transistors Contact resistance Organic semiconductors Thin-?lm morphology Dinaphthothienothiophene (DNTT)
abstract
Low-voltage organic thin-?lm transistors (TFTs) based on four different small-molecule semiconductors (pentacene, DNTT (dinaphtho[2,3-b:20,30-f]thieno[3,2-b]thiophene), C10-DNTT and DPh-DNTT) were fabricated, and a detailed comparison of the semiconductor thin-?lm morphology, of the current-voltage
characteristics of transistors with channel lengths ranging from 100 to 1 mm, and of the contact re-
sistances is provided. The three thienoacene derivatives DNTT, C10-DNTT and DPh-DNTT all have signi?cantly larger charge-carrier mobilities and smaller contact resistances than pentacene. In terms of the intrinsic channel mobility (determined using the transmission line method), C10-DNTT and DPhDNTT perform quite similarly and notably better than DNTT, suggesting that the decyl substituents in C10-DNTT and the phenyl substitue
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