An efficient solution-processable non-doped hybridized local and charge-transfer (HLCT) emitter for a simplified organic light-emitting diode
Here, a new solution-processable hybridized local and charge-transfer (HLCT) fluorescent molecule, CPBzFC , is designed and synthesized as an efficient emitter for low-cost and simple-structured electroluminescent devices. CPBzFC contains 7-(4-(carbazol- N -yl)phenyl)benzothiadiazole as an HLCT frag...
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Veröffentlicht in: | Materials chemistry frontiers 2022-10, Vol.6 (21), p.3225-3236 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Here, a new solution-processable hybridized local and charge-transfer (HLCT) fluorescent molecule,
CPBzFC
, is designed and synthesized as an efficient emitter for low-cost and simple-structured electroluminescent devices.
CPBzFC
contains 7-(4-(carbazol-
N
-yl)phenyl)benzothiadiazole as an HLCT fragment directly linked to a hole-transporting and highly soluble 7-(3,6-di-
tert
-butylcarbazol-
N
-yl)-9,9′-bis(8-(3,6-di-
tert
-butylcarbazol-
N
-yl)octyl)fluorene part. The photophysical results and theoretical calculations unveil an HLCT excited-state character with a strong yellowish-green fluorescence emission (a solid-state photoluminescence quantum yield of 82%), decent hole-transporting mobility, good film morphology, and thermal and electrochemical stabilities.
CPBzFC
is successfully utilized as a solution-processed non-doped emitter in simple structured OLEDs. This device achieves excellent electroluminescence (EL) performance with an ultra-high brightness of 30 800 cd m
−2
, a maximum external quantum efficiency (EQE
max
)of 6.74%, a maximum current efficiency (CE
max
) of 14.38 cd A
−1
, and a high exciton utilization efficiency (EUE) of 41%.
A solution-processable HLCT fluorescent molecule realizes a highly efficient non-doped OLED with a high brightness of 30 800 cd m
−2
, a maximum external quantum efficiency (EQE
max
) of 6.74% and a maximum current efficiency (CE
max
) of 14.38 cd A
−1
. |
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ISSN: | 2052-1537 2052-1537 |
DOI: | 10.1039/d2qm00401a |