Spirofluorene-locked carbazole based multiple resonance thermally activated delayed fluorescence emitters for efficient solution-processed narrowband green OLEDs?

Journal of Materials Chemistry C Pub Date: 2023-06-13 DOI: 10.1039/D3TC01321A

Abstract

Two kinds of multiple resonance thermally activated delayed fluorescence emitters namely SpDCz and DSpDCz are developed for solution-processed narrowband green organic light-emitting diodes (OLEDs) by fusing spirofluorene-locked carbazole moieties into the periphery of a boron, nitrogen-doped polycyclic aromatic hydrocarbon skeleton. Compared to the parent polycyclic aromatic skeleton with blue emission, SpDCz and DSpDCz exhibit longer emission wavelengths in the green region (λem = 498–505 nm) owing to the extended frontier molecular orbital distributions on the spirofluorene-locked carbazole moieties. Meanwhile, the photoluminescence quantum efficiency of the MR-TADF emitters is retained at up to 97–99% in solid-state films owing to the suppressed non-radiative transitions of excited states by the rigid and locked orthogonal configuration between outer carbazole and the polycyclic aromatic skeleton. Solution-processed OLEDs employing DSpDCz bearing two spirofluorene-locked carbazole moieties as emitters exhibit pure green electroluminescence at 505 nm with a FWHM of 31 nm and CIE coordinates of (0.13, 0.62), together with a maximum external quantum efficiency of 19.0%, representing a promising device efficiency for solution-processed narrowband green OLEDs.

Graphical abstract: Spirofluorene-locked carbazole based multiple resonance thermally activated delayed fluorescence emitters for efficient solution-processed narrowband green OLEDs
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