Efficient and multifunctional deep-blue organic luminescent materials are in great demand for the development of organic light-emitting diodes (OLEDs) in the application of ultrahigh-definition displays with a wide color gamut...
A violet-blue OLED derived from an orthogonal phenanthroimidazole-substituted 1,2,4-triazole fluorophore achieved a high EQE of 6.01% and CIEy of 0.043, being close to the blue standard of Rec.2020.
Efficient and stable deep-blue organic luminescent materials are important but rare for the application in full-color display due to their intrinsic wide bandgap characteristics. Here, a high-performance deep-blue hybridized local...
Traditional donor‐acceptor type organic luminescent materials usually suffer from unfavorable spectral broadening and fluorescence quenching problems arising from strong inter/intra‐chromophore interactions in aggregation state. Here, two ultraviolet carbazole‐pyrimidine isomers (named o‐DCz‐Pm and m‐DCz‐Pm) with novel aggregation‐induced narrowband phenomenon are constructed and systematic investigated by experiments and theoretical simulations. Benefitting from strengthened steric hindrance and multiple noncovalent interactions, the nonradiative decay, vibrational motion, and structural relaxation of singlet state can be effectively suppressed in aggregation state. Consequently, the electroluminescence peak of 397 nm, full width at half maximum of 21 nm and external quantum efficiency of 3.4% are achieved simultaneously in nondoped o‐DCz‐Pm‐based device. This work paves an avenue toward the development of high‐performance narrowband nondoped ultraviolet materials and organic light‐emitting diodes.
Achieving ultraviolet and narrowband emission simultaneously in nondoped organic light-emitting diodes (OLEDs) remains a tremendous challenge. Here, a "space-crowded donor−acceptor− donor" molecular design strategy is proposed for developing ultraviolet pure organic fluorophores by the nearby substituted positions at the phenyl linker between carbazole and pyridine units. Benefitting from the large steric hindrance effect, multiple intramolecular interactions, and low-frequency vibronic coupling dominated excited state property, all the emitters exhibit excellent fluorescence efficiencies at the solid state as well as the narrow full width at half maximums (FWHMs). Moreover, the effect of different substitution positions of pyridine on the structure−property relationship is also revealed. Consequently, the nondoped OLEDs exhibit an electroluminescence emission peak of 397 nm with FWHMs of 17 and 22 nm. Due to the high-lying reverse intersystem crossing process, external quantum and exciton utilization efficiencies of 3.6 and 54.55%, respectively, have been achieved based on the emitter with para-linkage. These findings may pave an avenue for the development of high-performance narrowband ultraviolet materials and OLEDs.
Realizing high-performance deep-blue fluorophores and non-doped organic light-emitting diodes (OLEDs) with the Commission international de I'Eclairage (CIE) coordinate of CIEy < 0.046 is important and challenging task for the wide...
Correction for ‘Regulation of excited-state properties of dibenzothiophene-based fluorophores for realizing efficient deep-blue and HLCT-sensitized OLEDs’ by Jichen Lv et al., Mater. Chem. Front., 2022, https://doi.org/10.1039/d2qm01008a.
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