Electroluminescence
(EL) from the singlet-excited (S1) state is the ideal choice
for stable, high-performing deep-blue
organic light-emitting diodes (OLEDs) owing to the advantages of an
adequately short radiative lifetime, improved device durability, and
low cost, which are the most important criteria for their commercialization.
Herein, we present the design and synthesis of three donor-acceptor-donor
(D–A–D)-configured deep-blue fluorescent materials (denoted
as TC–1, TC–2, and TC–3) composed of a thioxanthone or diphenyl sulfonyl acceptor and phenyl
carbazolyl donor. These systems exhibit strong deep-blue photoluminescence
(422–432 nm) in solutions and redshifted emission (472–486
nm) in thin films. The solid-state photoluminescence quantum yield
(PLQY) was estimated to be 78 and 94% for TC–2 and TC–3, respectively. TC–2 and TC–3 possess good molecular packing and
large molecular cross-sectional areas, which not only improves the
PLQY but enhances the triplet–triplet annihilation up-conversion
(TTAUC) efficiency of fluorescent emitters. Furthermore, both compounds
were applied as an acceptor for confirming their TTAUC property using
bis(2-methyldibenzo[f,h]quinoxaline)(acetylacetonate)iridium(III)
(Ir(MDQ)2acac) as the sensitizer. Non-doped OLEDs based
on TC–2 and TC–3 exhibit blue
EL in the 461–476 nm range. In particular, TC–3 exhibits a maximum external quantum efficiency (EQEmax) of 5.1%, and its EL maximum is 476 nm. In addition, the three emitters
were employed as hosts in red OLEDs using bis(1-phenylisoquinoline)(acetylacetonate)iridium(III)
(Ir(piq)2acac) as the phosphorescent dopant. The red phosphorescent
OLEDs based on TC–1, TC–2,
and TC–3 achieve excellent EQEmax values
of 21.6, 22.9, and 21.9%, respectively, and peak luminance efficiencies
of 12.0, 14.0, and 12.3 cd A–1. These results highlight
these fluorophores’ versatility and promising prospects in
practical OLED applications.