Universal Display Corporation

About: Universal Display Corporation is a company organization based out in Trenton, New Jersey, United States. It is known for research contribution in the topics: OLED & Layer (electronics). The organization has 323 authors who have published 622 publications receiving 21320 citations. The organization is also known as: UDC.

White Organic Light‐Emitting Devices for Solid‐State Lighting

Abstract: White organic light-emitting devices (WOLEDs) have advanced over the last twelve years to the extent that these devices are now being considered as efficient solid-state lighting sources. Initially, WOLEDs were targeted towards display applications for use primarily as liquid-crystal display backlights. Now, their power efficiencies have surpassed those of incandescent sources due to improvements in device architectures, synthesis of novel materials, and the incorporation of electrophosphorescent emitters. This review discusses the advantages and disadvantages of several WOLED architectures in terms of efficiency and color quality. Hindrances to their widespread acceptance as solid-state lighting sources are also noted.

Blue organic electrophosphorescence using exothermic host-guest energy transfer

Abstract: We demonstrate efficient blue electrophosphorescence using exothermic energy transfer from a host consisting of N,N′-dicarbazolyl-3,5-benzene (mCP) to the phosphorescent iridium complex iridium(III)bis[(4,6-difluorophenyl)-pyridinato-N,C2′]picolinate (FIrpic). By examining the temperature dependence of the radiative lifetime and the photoluminescence of a film of mCP doped with FIrpic, we confirm the existence of exothermic energy transfer in contrast to the endothermic transfer characteristic of the N,N′-dicarbazolyl-4-4′-biphenyl and FIrpic system. In employing exothermic energy transfer between mCP and FIrpic, a maximum external electroluminescent quantum efficiency of (7.5±0.8)% and a luminous power efficiency of (8.9±0.9)lm/W are obtained, representing a significant increase in performance over previous endothermic blue electrophosphorescent devices.

Endothermic energy transfer: A mechanism for generating very efficient high-energy phosphorescent emission in organic materials

Abstract: Intermolecular energy transfer processes typically involve an exothermic transfer of energy from a donor site to a molecule with a substantially lower-energy excited state (trap). Here, we demonstrate that an endothermic energy transfer from a molecular organic host (donor) to an organometallic phosphor (trap) can lead to highly efficient blue electroluminescence. This demonstration of endothermic transfer employs iridium(III)bis(4,6-di-fluorophenyl)-pyridinato-N,C2′)picolinate as the phosphor. Due to the comparable energy of the phosphor triplet state relative to that of the 4,4′-N,N′-dicarbazole-biphenyl conductive host molecule into which it is doped, the rapid exothermic transfer of energy from phosphor to host, and subsequent slow endothermic transfer from host back to phosphor, is clearly observed. Using this unique triplet energy transfer process, we force emission from the higher-energy, blue triplet state of the phosphor (peak wavelength of 470 nm), obtaining a very high maximum organic light-emi...

High-efficiency red electrophosphorescence devices

Abstract: We demonstrate high-efficiency red electrophosphorescent organic light-emitting devices employing bis(2-(2′-benzo[4,5-a]thienyl)pyridinato-N,C3′) iridium(acetylacetonate) [Btp2Ir(acac)] as a red phosphor. A maximum external quantum efficiency of ηext=(7.0±0.5)% and power efficiency of ηp=(4.6±0.5) lm/W are achieved at a current density of J=0.01 mA/cm2. At a higher current density of J=100 mA/cm2, ηext=(2.5±0.3)% and ηp=(0.56±0.05) lm/W are obtained. The electroluminescent spectrum has a maximum at a wavelength of λmax=616 nm with additional intensity peaks at λsub=670 and 745 nm. The Commission Internationale de L’Eclairage coordinates of (x=0.68, y=0.32) are close to meeting video display standards. The short phosphorescence lifetime (∼4 μs) of Btp2Ir(acac) leads to a significant improvement in ηext at high currents as compared to the previously reported red phosphor, 2,3,7,8,12,13,17,18-octaethyl-12H, 23H-prophine platinum (II) PtOEP with a lifetime of ∼50 μs.

100% phosphorescence quantum efficiency of Ir(III) complexes in organic semiconductor films

Abstract: We demonstrate that three Ir(III) complexes used as principal dopants in organic electrophosphorescent diodes have very high photoluminescence quantum efficiency (ηPL) in a solid-state film. The green emitting complex, fac-tris(2-phenylpyridinato)iridium(III) [Ir(ppy)3], the red-emitting bis[2-(2′-benzothienyl)pyridinato-N,C3′] (acetylacetonato)iridium(III) [Btp2Ir(acac)], and the blue complex bis[(4,6-difluorophenyl)pyridinato-N,C2](picolinato)iridium(III) (FIrpic) were prepared as codeposited films of varying concentration with 4,4′-bis(N-carbazolyl)-2,2′-biphenyl, a commonly used host material. The maximum ηPL values for Ir(ppy)3, Btp2Ir(acac), and FIrpic were, respectively, 97%±2% (at 1.5mol%), 51%±1% (at 1.4mol%), and 78%±1% (at 15mol%). Furthermore, we also observed that the maximum ηPL of FIrpic reached 99%±1% when doped into the high triplet energy host, m-bis(N-carbazolyl)benzene, at an optimal concentration of 1.2mol%.