RESUMEN
Phosphorescent molecular aggregates show promise in realizing efficient and stable organic light-emitting diodes (OLEDs) operating at high brightness level, which is highly desired for future lighting and display applications. Herein, four tetradentate Pd(II) complexes are prepared with judicious ligand design, and their electrochemical and photophysical properties are thoroughly examined. The studies indicate that slight structural changes of ligands can modify the hole and electron transporting capabilities, and alter the horizontal emitting dipole ratios of aggregates in amorphous film, the latter of which are sensitive to the thin-film deposition conditions including the deposition rate and the choice of the templating layer. An optimized OLED device using Pd3O8-Py5 aggregates exhibits a peak external quantum efficiency (EQE) of 37.3% and a reduced efficiency roll-off with high EQEs of 36.0% and 32.5% at 1000 and 10 000 cd m-2 , respectively. Moreover, such an efficient device demonstrates a long measured LT95 (time to 95% of the initial luminance) lifetime of over 500 h with an initial brightness of 17 304 cd m-2 corresponding to an estimated LT95 lifetime of 48 246 h at 1000 cd m-2 .
RESUMEN
A novel host material of "M"-type carbazole/fluorene-based mDCzPF with a high triplet energy by utilizing meta-substituted phenyl groups as linkers was developed. It was demonstrated that the position of the substituents significantly affected the molecular configuration and dipole moment, which played a critical role in the device performances. Red phosphorescent OLED utilizing the "M"-type mDCzPF as the host represented a 10-fold operational lifetime improvement over the OLED using a "V"-type pDCzPF linked by para-substituted phenyl groups as the host because of the good charge transport ability of the mDCzPF. Additionally, the "M"-type mDCzPF host was also compatible with a blue emitting phosphorescent emitter PtNON. The PtNON-doped OLED using mDCzPF as the host exhibited a peak EQE of 18.3% with a small roll off, yet maintained an EQE of 13.3% at a high brightness of 5000 cd/m2. Thus, the novel "M"-type mDCzPF could be employed as stable host material for efficient OLED emitting across the whole visible spectrum. This study should provide a viable method for designing new host materials for the development of stable and efficient phosphorescent OLEDs.
RESUMEN
A tetradentate cyclometalated Pt(II) complex (PtN3N) is developed as an efficient, stable phosphorescent emitter. One PtN3N device exhibits an estimated LT97 of 2057 h at an initial luminance of 1000 cd m-2 , while maintaining an external quantum efficiency of 15.3% at such high brightness, demonstrating performance to overcome the last technical barrier to the commercialization of Pt complexes for many applications.
RESUMEN
We report the development of efficient small molecular organic photovoltaic devices incorporating tetracene anode interfacial layers. Planar heterojunction devices employing the tetracene anode interfacial layer achieved an EQE enhancement of 150% in the spectral region corresponding to ZnPc absorption. We demonstrate that this enhancement is due to the combined effect of the tetracene layer providing exciton-blocking at the anode/donor interface and potentially an increase in the exciton diffusion length in the ZnPc layer due to increased crystallinity and more preferred molecular stacking orientation. A power conversion efficiency of 4.7% was achieved for a planar heterojunction of a modified zinc phthalocyanine based material and C60 when employing the tetracene anode interfacial layer. By utilizing a planar-mixed heterojunction structure a peak EQE of nearly 70% and a power conversion efficiency of 5.8% was achieved.