Anthracene derivatives are one of the most promising blue emitters employed in organic light-emitting devices (OLEDs) because of their electrochemical and thermal stabilities. However, their high crystallinity owing to their large π-planar structures severely impedes the progress in the development of solution-based systems. In this work, we developed two types of highly soluble multifunctional anthracene derivatives terminated with ortho-biphenyl and triphenylamine moieties and showed high solubility in general organic solvents such as toluene, tetrahydrofuran, and cyclohexanone at high concentrations (>10 mg mL ), and showed blue emission with a peak wavelength of ∼465 nm and a high photoluminescence quantum yield that ranges up to 81 %.
View Article and Find Full Text PDFInvited for the cover of this issue is Hisahiro Sasabe, Junji Kido and co-workers at Yamagata University in Japan. This image depicts that the chemical structure of the acceptor is one of the most important keys to maximize the potential of triazine/acridine-based thermally activated delayed fluorescence (TADF) emitters realizing high external quantum efficiency (EQE) of over 30%. Read the full text of the article at 10.
View Article and Find Full Text PDFRecently, researchers have focused on thermally activated delayed fluorescence (TADF) for efficient future lighting and displays. Among TADF emitters, a combination of triazine and acridine is a promising candidate for realizing high-efficiency organic light-emitting devices (OLEDs). However, simultaneous development of perfect horizontal orientation (Θ=100 %) and an external quantum efficiency (EQE) of over 40 % is still challenging.
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