Derivatives of 2-Pyridone Exhibiting Hot-Exciton TADF for Sky-Blue and White OLEDs.

Development of emissive materials for utilization in organic light-emitting diodes (OLEDs) remains a highly relevant research field. One of the most important aspects in the development of efficient emitters for OLEDs is the efficiency of triplet-to-singlet exciton conversion. There are many concepts proposed for the transformation of triplet excitons to singlet excitons, among which thermally activated delayed fluorescence (TADF) is the most efficient and widespread. One of the variations of the TADF concept is the hot exciton approach according to which the process of exciton relaxation into the lowest energy electronic state (internal conversion as usual) is slower than intersystem crossing between high-lying singlets and triplets. In this paper, we present the donor-acceptor materials based on 2-pyridone acceptor coupled to the different donor moieties through the phenyl linker demonstrating good performance as components of sky-blue, green-yellow, and white OLEDs. Despite relatively low photoluminescence quantum yields, the compound containing 9,9-dimethyl-9,10-dihydroacridine donor demonstrated very good efficiency in sky-blue OLED with the single emissive layer, which showed an external quantum efficiency (EQE) of 3.7%. It also forms a green-yellow-emitting exciplex with 4,4',4″-tris[phenyl(m-tolyl)amino]triphenylamine. The corresponding OLED showed an EQE of 6.9%. The white OLED combining both exciplex and single emitter layers demonstrated an EQE of 9.8% together with excellent current and power efficiencies of 16.1 cd A-1 and 6.9 lm W-1, respectively. Quantum-chemical calculations together with the analysis of photoluminescence decay curves confirm the ability of all of the studied compounds to exhibit TADF through the hot exciton pathway, but the limiting factor reducing the efficiency of OLEDs is the low photoluminescence quantum yields caused mainly by nonradiative intersystem crossing dominating over the radiative fluorescence pathway.

Mixing of phosphorescent and exciplex emission in efficient organic electroluminescent devices.

We fabricated a yellow organic light-emitting diode (OLED) based on the star-shaped donor compound tri(9-hexylcarbazol-3-yl)amine, which provides formation of the interface exciplexes with the iridium(III) bis[4,6-difluorophenyl]-pyridinato-N,C2']picolinate (FIrpic). The exciplex emission is characterized by a broad band and provides a condition to realize the highly effective white OLED. It consists of a combination of the blue phosphorescent emission from the FIrpic complex and a broad efficient delayed fluorescence induced by thermal activation with additional direct phosphorescence from the triplet exciplex formed at the interface. The fabricated exciplex-type device exhibits a high brightness of 38 000 cd/m(2) and a high external quantum efficiency.