TY - JOUR
T1 - Extended and Modulated Thienothiophenes for Thermally Durable and Solution-Processable Organic Semiconductors
AU - Inoue, Satoru
AU - Shinamura, Shoji
AU - Sadamitsu, Yuichi
AU - Arai, Shunto
AU - Horiuchi, Sachio
AU - Yoneya, Makoto
AU - Takimiya, Kazuo
AU - Hasegawa, Tatsuo
N1 - Funding Information:
This study was partly supported by Grants-in-Aid for Scientific Research (A) (Grant 18H03875), for Young Scientist (B) (Grant 17K14370), and on Innovative Areas (Grant 17H05144) from the Japan Society for the Promotion of Science (JSPS). S.A. also is thankful for the support from Nanotech CUPAL from JST. The synchrotron X-ray experiment was performed with the approval of the Photon Factory Program Advisory Committee (2014S2-001 and 2017S2-001). The thin-film X-ray diffraction experiments were conducted at the Advanced Characterization Nanotechnology Platform of the University of Tokyo, supported by “Nanotechnology Platform” of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/8/14
Y1 - 2018/8/14
N2 - Herein, we report the rational design of practical small-molecule organic semiconductors based on a π-electron skeleton of benzothieno[3,2-b]naphtho[2,3-b]thiophene (BTNT) whose layered herringbone (LHB) packing is intentionally modulated by the designated asymmetric substitutions with the phenyl group and normal alkyl chains. The thermal stability of the hybrid BTNT core is high enough, as it lies between those of dinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene (DNTT) and benzothieno[3,2-b]benzothiophene (BTBT), although the solvent solubility for the substituted BTNT at ordinary 2,8-substituting positions by the alkyl chain and phenyl group remains extremely low. We show in the BTBT and BTNT derivatives that the tuning of the substituting position works to slightly bend the rodlike organic semiconductor molecules and thus to decrease the cohesive energy of the crystals with retention of the bilayer-type herringbone (b-LHB) packing for the asymmetric rodlike molecules. This modification eventually leads to an increase in solvent solubility, a decrease in phase transition temperature, and the suppression of liquid-crystalline phases at high temperatures. By using the substituting effect, we successfully achieve the organic semiconductors with modulated alkylated Ph-BTNT that exhibits both a sufficiently high solvent solubility and a sufficiently high thermal stability. The variation in the crystal packing also enhances the intermolecular transfer integrals along the T-shaped contacts within the intralayer herringbone packing. Spin coating of the material under ambient conditions affords high-performance bottom-gate, bottom-contact organic thin-film transistors, exhibiting high thermal durability in the device characteristics below 150 °C. The obtained devices also exhibit a higher mobility, a lower threshold voltage, and a smaller subthreshold swing, by initial thermal treatment at 140 °C, composed to those of the as-prepared films, because the thermal treatment stabilizes the b-LHB packing and thus suppresses the residual minority holes and shallow traps. These findings should be crucial in the design and development of organic semiconductor materials for practical printed electronics applications.
AB - Herein, we report the rational design of practical small-molecule organic semiconductors based on a π-electron skeleton of benzothieno[3,2-b]naphtho[2,3-b]thiophene (BTNT) whose layered herringbone (LHB) packing is intentionally modulated by the designated asymmetric substitutions with the phenyl group and normal alkyl chains. The thermal stability of the hybrid BTNT core is high enough, as it lies between those of dinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene (DNTT) and benzothieno[3,2-b]benzothiophene (BTBT), although the solvent solubility for the substituted BTNT at ordinary 2,8-substituting positions by the alkyl chain and phenyl group remains extremely low. We show in the BTBT and BTNT derivatives that the tuning of the substituting position works to slightly bend the rodlike organic semiconductor molecules and thus to decrease the cohesive energy of the crystals with retention of the bilayer-type herringbone (b-LHB) packing for the asymmetric rodlike molecules. This modification eventually leads to an increase in solvent solubility, a decrease in phase transition temperature, and the suppression of liquid-crystalline phases at high temperatures. By using the substituting effect, we successfully achieve the organic semiconductors with modulated alkylated Ph-BTNT that exhibits both a sufficiently high solvent solubility and a sufficiently high thermal stability. The variation in the crystal packing also enhances the intermolecular transfer integrals along the T-shaped contacts within the intralayer herringbone packing. Spin coating of the material under ambient conditions affords high-performance bottom-gate, bottom-contact organic thin-film transistors, exhibiting high thermal durability in the device characteristics below 150 °C. The obtained devices also exhibit a higher mobility, a lower threshold voltage, and a smaller subthreshold swing, by initial thermal treatment at 140 °C, composed to those of the as-prepared films, because the thermal treatment stabilizes the b-LHB packing and thus suppresses the residual minority holes and shallow traps. These findings should be crucial in the design and development of organic semiconductor materials for practical printed electronics applications.
UR - http://www.scopus.com/inward/record.url?scp=85050604060&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85050604060&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.8b01339
DO - 10.1021/acs.chemmater.8b01339
M3 - Article
AN - SCOPUS:85050604060
SN - 0897-4756
VL - 30
SP - 5050
EP - 5060
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 15
ER -