4.8 Article

Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 48, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202104638

Keywords

ambipolar charge transport; electroluminescence; fluorination; light-emitting transistor; organic optoelectronics

Funding

  1. RSF [18-12-00499, 20-73-10090]
  2. State Assignment of Ministry of Science and Higher Education of Russian Federation [0238-2019-0004]
  3. Russian Science Foundation [18-12-00499, 20-73-10090] Funding Source: Russian Science Foundation

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The selective fluorination of FPCOs lowers the energies of frontier molecular orbitals, improving the photostability, tuning the pi-pi stacked packing, and allowing the first realization of electron transport in FPCOs. Selectively fluorinated 2,2'- (2,3,5,6-tetrafluoro-1,4-phenylene) bis[5-(3,5-difluorophenyl) furan] demonstrates well-balanced ambipolar charge transport and efficient electroluminescence in an OLET with high external quantum and luminous efficiencies. Smart fluorination is a powerful tool to fine-tune the stability and performance of linearly conjugated small molecules for organic optoelectronics.
Linearly conjugated oligomers attract ever-growing attention as promising systems for organic optoelectronics because of their inherent lucky combination of high charge mobility and bright luminescence. Among them, furan-phenylene co-oligomers (FPCOs) are distinguished by outstanding solubility, very bright luminescence, and good hole-transport properties; however, furan-containing organic semiconductors generally lack electron transport, which makes it impossible to utilize them in efficient light-emitting electronic devices, specifically, ambipolar light-emitting transistors. In this work, 1,4-bis(5-phenylfuran-2-yl)benzene (FP5) derivatives are synthesized with the fully/partially fluorinated central and edge phenyl rings. It is shown that the selective fluorination of FPCOs lowers the energies of frontier molecular orbitals, maintaining the bandgap, solubility, and bright luminescence, dramatically improves the photostability, tunes the pi-pi stacked packing, and allows the first realization of electron transport in FPCOs. It is found that selectively fluorinated 2,2 '-(2,3,5,6-tetrafluoro-1,4-phenylene)bis[5-(3,5-difluorophenyl)furan] demonstrates well-balanced ambipolar charge transport and efficient electroluminescence in an organic light-emitting transistor (OLET) with external quantum and luminous efficiencies as high as 0.63% and 5 cdA(-1), respectively, which are among the best reported for OLETs. The findings show that smart fluorination is a powerful tool to fine-tune the stability and performance of linearly conjugated small molecules for organic optoelectronics.

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