A new rod-shaped BODIPY-acetylene molecule for solution-processed semiconducting microribbons in n-channel organic field-effect transistors

• Published in: New journal of chemistry 2017, Vol.41 (14), p.6232-6240
• Main Authors: Ozdemir, Mehmet, Choi, Donghee, Zorlu, Yunus, Cosut, Bunyemin, Kim, Hyungsug, Kim, Choongik, Usta, Hakan
• Format: Article
• Language: English
• ISSN: 1144-0546; 1369-9261
• DOI: 10.1039/C7NJ00266A

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 of BDY-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.