Tetradentate Pt(II) Complexes with Bulky Carbazole Moieties for High-Efficiency and Narrow-Emitting Blue Organic Light-Emitting Devices.

Abstract

Blue tetradentate Pt(II) complexes, Pt-tBuCz and Pt-dipCz, are synthesized by introducing carbazoles with bulky substituents for improving the rigidity and inhibiting intermolecular interactions of phosphorescent emitter. tert-Butyl and 2,6-diisopropylphenyl groups are substituted as the blocking groups at 3 position of the carbazole in Pt-tBuCz and Pt-dipCz, respectively. These new phosphorescent emitters exhibit a narrow full width at half maximum (FWHM) and a high horizontal emitting dipole orientation ratio. Pt-dipCz demonstrates a small FWHM of 24nm, a high emitting dipole orientation ratio of 81%, and a high photoluminescence quantum yield value of 94%. As a result, the Pt-tBuCz and Pt-dipCz devices exhibited external quantum efficiencies (EQEs) of 23.7% and 25.0% with small FWHMs of 25 and 22nm, respectively. For the Pt-dipCz device, the small FWHM and high EQE of >20% are maintained even at a doping concentration of 20 wt%. Furthermore, phosphor-sensitized organic light-emitting diodes fabricated using Pt-dipCz as a sensitizer achieved a high EQE of 31.4% with an FWHM of 18nm. This result indicates that the 2,6-diisopropylphenyl group is a effective blocking group for Pt(II) complexes to develop highly efficient, color stable, doping concentration resistant, and efficiently sensitizing blue phosphors.