A new rod-shaped BODIPY-acetylene molecule for solution-processed semiconducting microribbons in n-channel organic field-effect transistors. (14th June 2017)
- Record Type:
- Journal Article
- Title:
- A new rod-shaped BODIPY-acetylene molecule for solution-processed semiconducting microribbons in n-channel organic field-effect transistors. (14th June 2017)
- Main Title:
- A new rod-shaped BODIPY-acetylene molecule for solution-processed semiconducting microribbons in n-channel organic field-effect transistors
- Authors:
- Ozdemir, Mehmet
Choi, Donghee
Zorlu, Yunus
Cosut, Bunyemin
Kim, Hyungsug
Kim, Choongik
Usta, Hakan - Abstract:
- Abstract : A novel solution-processable BODIPY-based small molecule (BDY-PhAc-BDY ) yields highly-crystalline, one-dimensional (1-D) microribbon semiconductors for organic field-effect transistors (OFETs). Abstract : BODIPY-based π-conjugated small molecules have been extensively studied in various fields of sensing and biochemical labelling; however, their use in organic optoelectronic applications is very limited. A new solution-processable acceptor–donor–acceptor (A–D–A) type small molecule, BDY-PhAc-BDY, consisting of BODIPY π-acceptors and a rod-shaped 1, 4-bis-(thienylethynyl)2, 5-dialkoxybenzene π-donor, has been synthesized and fully characterized as a novel n-channel semiconductor in bottom-gate/top-contact organic field-effect transistors (OFETs). The new semiconductor exhibits an electrochemical band gap of 2.12 eV with highly stabilized HOMO/LUMO energy levels of −5.68 eV/−3.56 eV. Single-crystal X-ray diffraction (XRD) analysis ofBDY-PhAc-BDY reveals a relatively low "BODIPY- meso -thiophene" dihedral angle ( θ = 44.94°), antiparallel π-stacked BODIPY dimers with an interplanar distance of 3.93 Å, and strong "C–H⋯π (2.85 Å)" interactions. The OFET devices fabricated by solution processing show the formation of highly-crystalline, one-dimensional (1-D) microribbons, which results in clear n-channel semiconductivity with an electron mobility of 0.004 cm 2 V −1 s −1 and an on/off current ratio of 10 5 –10 6 . To date, this is the highest reported for BODIPY-basedAbstract : A novel solution-processable BODIPY-based small molecule (BDY-PhAc-BDY ) yields highly-crystalline, one-dimensional (1-D) microribbon semiconductors for organic field-effect transistors (OFETs). Abstract : BODIPY-based π-conjugated small molecules have been extensively studied in various fields of sensing and biochemical labelling; however, their use in organic optoelectronic applications is very limited. A new solution-processable acceptor–donor–acceptor (A–D–A) type small molecule, BDY-PhAc-BDY, consisting of BODIPY π-acceptors and a rod-shaped 1, 4-bis-(thienylethynyl)2, 5-dialkoxybenzene π-donor, has been synthesized and fully characterized as a novel n-channel semiconductor in bottom-gate/top-contact organic field-effect transistors (OFETs). The new semiconductor exhibits an electrochemical band gap of 2.12 eV with highly stabilized HOMO/LUMO energy levels of −5.68 eV/−3.56 eV. Single-crystal X-ray diffraction (XRD) analysis ofBDY-PhAc-BDY reveals a relatively low "BODIPY- meso -thiophene" dihedral angle ( θ = 44.94°), antiparallel π-stacked BODIPY dimers with an interplanar distance of 3.93 Å, and strong "C–H⋯π (2.85 Å)" interactions. The OFET devices fabricated by solution processing show the formation of highly-crystalline, one-dimensional (1-D) microribbons, which results in clear n-channel semiconductivity with an electron mobility of 0.004 cm 2 V −1 s −1 and an on/off current ratio of 10 5 –10 6 . To date, this is the highest reported for BODIPY-based small molecular semiconductors with alkyne linkages. Our results clearly demonstrate that BODIPY is an effective π-acceptor unit for the design of solution-processable, electron-transporting organic semiconductors and easily fabricable 1-D semiconductor micro-/nano-structures for fundamental/applied research in organic optoelectronics. … (more)
- Is Part Of:
- New journal of chemistry. Volume 41:Number 14(2017)
- Journal:
- New journal of chemistry
- Issue:
- Volume 41:Number 14(2017)
- Issue Display:
- Volume 41, Issue 14 (2017)
- Year:
- 2017
- Volume:
- 41
- Issue:
- 14
- Issue Sort Value:
- 2017-0041-0014-0000
- Page Start:
- 6232
- Page End:
- 6240
- Publication Date:
- 2017-06-14
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c7nj00266a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2855.xml