Abstract:Device degradation in red hyperfluorescent organic light-emitting diodes is primarily caused by exciton energy loss due to Dexter energy transfer (DET) from a thermally activated delayed fluorescence (TADF) assistant dopant to a fluorescent dopant. In this work, the donor segments in the TADF assistant dopants were delicately modulated to suppress DET for high efficiency. The derived benzothienocarbazole donors were introduced to the TADF assistant dopants instead of carbazole, and they accelerated the reverse… Show more
“…However, the 12BTCzTPN device showed slightly improved efficiency roll-off due to its higher rISC rate, which was attributed to the heavy-atom effect of the sulfur . Lee et al reported that red hyperfluorescent OLEDs fabricated with three benzothienocarbazole-based emitters (PLQY = 25–36%) showed slightly higher EQ E max values in the range of 12.3–14.7% compared to a carbazole counterpart (EQE max 11.3%) . These benzothienocarbazole-based derivatives also showed shorter DF lifetimes as compared to their nonsulfur TADF congeners.…”
Section: Resultsmentioning
confidence: 99%
“…Benzothienocarbazoles are relatively unexplored donor systems for designing TADF emitters, ,,, and so it was of particular interest to isolate any potential heavy-atom effect of sulfur by comparison with the parent carbazole analogue Cz-CF3 . Due to the relatively weaker donor strength of Cz compared to TCz, 1 wt % zeonex films of Cz-CF3 showed deeper-blue emission compared to TCz-CF3 and with a relatively large Δ E ST of 0.15 eV (Figure d, Table S5).…”
The efficiency of thermally activated delayed fluorescence (TADF) in organic materials relies on rapid intersystem crossing rates and fast conversion of triplet (T) excitons into a singlet (S) state. Heavy atoms such as sulfur or selenium are now frequently incorporated into TADF molecular structures to enhance these properties by increased spin−orbit coupling [spin orbit coupling (SOC)] between the T and S states. Here a series of donor−acceptor (D−A) molecules based on 12Hbenzo [4,5]thieno[2,3-a]carbazole and dicyanopyridine is compared with their nonsulfur control molecules designed to probe such SOC effects. We reveal that unexpected intermolecular interactions of the D−A molecules with carbazolecontaining host materials instead serve as the dominant pathway for triplet decay kinetics in these materials. In-depth photophysical and computational studies combined with organic light emitting diode measurements demonstrate that the anticipated heavy-atom effect from sulfur is overshadowed by exciplex formation. Indeed, even the unsubstituted acceptor fragments exhibit pronounced TADF exciplex emission in appropriate carbazole hosts. The intermolecular charge transfer and TADF in these systems are further confirmed by detailed time-dependent density functional theory studies. This work demonstrates that anticipated heavy-atom effects in TADF emitters do not always control or even impact the photophysical and electroluminescence properties.
“…However, the 12BTCzTPN device showed slightly improved efficiency roll-off due to its higher rISC rate, which was attributed to the heavy-atom effect of the sulfur . Lee et al reported that red hyperfluorescent OLEDs fabricated with three benzothienocarbazole-based emitters (PLQY = 25–36%) showed slightly higher EQ E max values in the range of 12.3–14.7% compared to a carbazole counterpart (EQE max 11.3%) . These benzothienocarbazole-based derivatives also showed shorter DF lifetimes as compared to their nonsulfur TADF congeners.…”
Section: Resultsmentioning
confidence: 99%
“…Benzothienocarbazoles are relatively unexplored donor systems for designing TADF emitters, ,,, and so it was of particular interest to isolate any potential heavy-atom effect of sulfur by comparison with the parent carbazole analogue Cz-CF3 . Due to the relatively weaker donor strength of Cz compared to TCz, 1 wt % zeonex films of Cz-CF3 showed deeper-blue emission compared to TCz-CF3 and with a relatively large Δ E ST of 0.15 eV (Figure d, Table S5).…”
The efficiency of thermally activated delayed fluorescence (TADF) in organic materials relies on rapid intersystem crossing rates and fast conversion of triplet (T) excitons into a singlet (S) state. Heavy atoms such as sulfur or selenium are now frequently incorporated into TADF molecular structures to enhance these properties by increased spin−orbit coupling [spin orbit coupling (SOC)] between the T and S states. Here a series of donor−acceptor (D−A) molecules based on 12Hbenzo [4,5]thieno[2,3-a]carbazole and dicyanopyridine is compared with their nonsulfur control molecules designed to probe such SOC effects. We reveal that unexpected intermolecular interactions of the D−A molecules with carbazolecontaining host materials instead serve as the dominant pathway for triplet decay kinetics in these materials. In-depth photophysical and computational studies combined with organic light emitting diode measurements demonstrate that the anticipated heavy-atom effect from sulfur is overshadowed by exciplex formation. Indeed, even the unsubstituted acceptor fragments exhibit pronounced TADF exciplex emission in appropriate carbazole hosts. The intermolecular charge transfer and TADF in these systems are further confirmed by detailed time-dependent density functional theory studies. This work demonstrates that anticipated heavy-atom effects in TADF emitters do not always control or even impact the photophysical and electroluminescence properties.
“…With the polycyclic aromatic hydrocarbon DBP as the fluorescent emitter hyperfluorescent 2BT12CzINN :DBP devices in a PBICT:DBTTP1 host had EQE max 14.7% and CIE(0.60, 0.39). 134 The EQE and the lifetime LT 90 of 41.8 h at L 0 3000 cd m −2 were improved compared to a reference 4CzTPN:DBP device (EQE max 11.3%; LT 90 27.8 h).…”
Section: Fused Carbazole Derivatives As Tadf Emittersmentioning
This review focuses on fused-ring carbazole derivatives, their molecular design, electronic and photophysical properties, and their applications as the emitter and/or the host material in organic light emitting diodes (OLEDs).
“…Donors of different chromophores, such as benzofurocarbazole and benzothienocarbazole, which are obtained by fusing carbazole with benzofuran or benzothiophene, have also been developed. [4][5][6] Recently, materials with improved rigidity, based on the v-DABNA backbone and known as HF materials, have been reported. 7,8 The second key principle involves conferring bipolar characteristics to maintain charge balance.…”
Three new blue materials, TPI-InCz, PAI-InCz, and CN-PAI-InCz, have been developed. Among the three materials, CN-PAI-InCz showed the highest external quantum efficiency of 3.31% with fast hole mobility of 1.50 × 10−3 cm2 V−1 s−1.
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