Abstract
Two cyano-substituted spiro[fluorine-9,9′-xanthene] (SFX) derivatives, 2-carbonitrile-spiro[fluorene-9,9′-xanthene] (CNSFX) and 2,7-dicarbonitrile-spiro[fluorene-9,9′-xanthene] (DCNSFX) were conveniently prepared as electron acceptors to combine with tris(4-carbazoyl-9-ylphenyl)amine (TCTA) as electron donor to form exciplex emitters, respectively. Favorable exciplex-TADF was successfully achieved with photoluminescence quantum yield of 31% and electroluminescence efficiency of 8.2 cd A−1 in TCTA:DCNSFX, which possesses increases of 1.1 and 3.3 times than those (15% and 1.9 cd A−1) of TCTA:CNSFX, respectively. The relatively favorable performance of TCTA:DCNSFX is related to the stronger electron-accepting ability through dicyano-substitution and larger driving force in the exciplex emission. These appealing results reveal that the dicyano-substituted SFX derivative opens interesting perspectives for developing favorable exciplex-TADF organic light-emitting diodes in the future.
Original language | English |
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Pages (from-to) | 422-429 |
Number of pages | 8 |
Journal | Dyes and Pigments |
Volume | 149 |
DOIs | |
State | Published - Feb 2018 |
Keywords
- Dicyano-substitution
- Exciplex
- Improved efficiencies
- Organic light-emitting diode
- Spiro[fluorine-9,9′-xanthene]
- Thermally activated delayed fluorescence