Organic light-emitting diodes (OLEDs) able to directly emit circularly polarized (CP) electroluminescence (CP-OLEDs) are rapidly gaining much interest, due to their possible applications in displays with antiglare filters and 3D displays. Development of more efficient CP-OLEDs can open their use also in point-of-care and personalized diagnostic tools, since CP light alteration can be related to health state of irradiated tissues. In this work it is shown that the performance of chiral europium complex-based CP-OLEDs can be improved both in terms of external quantum efficiency (measured on all the Eu bands) and degree of polarization of emitted photons (as measured by the dissymmetry factor gEL), by proper active layer formulation and through a fine tuning of the architecture of the device. Polarization performances (gEL = −1) are obtained about three times higher than for any other CP-OLED reported so far. Moreover, for the first time, it is shown that the position of the recombination zone (RZ) plays a major role on the polarization outcomes. In order to rationalize these results the level of light polarization is related to the position of the RZ allied with the reflection on the cathode through a simple mathematical model. The values predicted by this model are in qualitative agreement with the experimental ones

No abstract

Purely organic materials showing solid state room temperature phosphorescence (RTP) are receiving an ever growing interest due to their low toxicity, cost and environmental load compared to their organometallic counterparts.

Solid-state luminescent materials with long lifetimes are the subject of ever-growing interest from both a scientific and a technological point of view. However, when dealing with organic compounds, the achievement of highly efficient materials is limited by aggregation-caused quenching (ACQ) phenomena on one side and by ultrafast deactivation of the excited states on the other. Here, we report on a simple organic molecule, namely, cyclic triimidazole (CHN), 1, showing crystallization-induced emissive (CIE) behavior and, in particular, ultralong phosphorescence due to strong coupling in H-aggregated molecules. Our experimental data reveal that luminescence lifetimes up to 1 s, which are several orders of magnitude longer than those of conventional organic fluorophores, can be realized under ambient conditions, thus expanding the class of organic materials for phosphorescence applications.