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We report high efficiency and low roll-off for blue electrophosphorescent organic light emitting devices based on a mixed host layer architecture. The devices were fabricated using a mixed layer of di-[4-(N,N-ditolyl-amino)-phenyl]cyclohexane, a hole transport material, and 2,8-bis(diphenylphosphoryl)dibenzothiophene, an electron transport material, as the host layer doped with the blue phosphor iridium (III) bis[(4,6-difluorophenyl)-pyridinato-N,C2′]picolinate. Using a mixed layer as the host allowed us to achieve high power efficiency (59 lm/W at 100 cd/m2), low turn-on voltage (2.7 V for >10 cd/m2), and low roll-off in these devices. [ABSTRACT FROM AUTHOR]

We report blue electrophosphorescent organic light emitting devices with an ambipolar host material, 4-(diphenylphosphoryl)-N,N-diphenylaniline (HM-A1), doped with FIrpic (iridium (III)bis[(4,6-difluorophenyl)-pyridinato-N,C2′]picolinate). The ambipolar nature of the host was verified using single carrier devices. The power efficiency of devices with PO15 (2,8-bis(diphenylphosphoryl)dibenzothiophene) electron transport layer (ETL) showed optimized performance when the ETL thickness was 500 Å, giving a peak power efficiency of 46 lm/W (corresponding external quantum efficiency (EQE) of 17.1%). The EQE and power efficiency at the brightness of 800 cd/m2 were measured with no light outcoupling enhancement and found to be 15.4% and 26 lm/W, respectively. [ABSTRACT FROM AUTHOR]

We demonstrate high efficiency white organic light-emitting devices with two adjacent emissive layers each doped with three phosphorescent emitters (blue, green, and red). Efficient charge and exciton confinement is realized by employing charge transport layers with high triplet energy, leading to a maximum external quantum efficiency of (19±1)%. Using the p-i-n device structure, we have achieved a peak power efficiency of (40±2) lm/W and (36±2) lm/W at 100 cd/m2, a color rendering index of 79, and Commission Internationale de L’Eclairage coordinates of (0.37, 0.40) for the white light emission. [ABSTRACT FROM AUTHOR]

We have demonstrated a substantial enhancement in the efficiency of iridium (III) bis[(4,6-di-fluorophenyl)-pyridinate-N,C2′]picolinate based blue phosphorescent organic light-emitting devices (PHOLEDs). The efficiencies of PHOLEDs with conventional electron transport materials are low due to their low electron mobilities as well low triplet energies. High triplet energy electron transporting material with high electron mobility was used as a hole blocker to achieve efficient exciton confinement and good charge balance in the device thereby achieving a high current efficiency of 49 cd/A and an external quantum efficiency of 23%. [ABSTRACT FROM AUTHOR]

We report on very high efficiency deep-blue phosphorescent organic light-emitting devices (PHOLEDs) based on iridium(III) bis(4′,6′-difluorophenylpyridinato)tetrakis(1-pyrazolyl)borate (FIr6). Dual emissive layers consisting of an N,N′-dicarbazolyl-3,5-benzene layer doped with 4 wt % FIr6 and a p-bis(triphenylsilyly)benzene layer doped with 25 wt % FIr6 were employed to maximize exciton generation on FIr6 molecules. Combined with the p-i-n device structure, we achieved a low turn-on voltage of 3.2 V and very high power efficiencies of 25±2 lm/W at 100 cd/m2 and 20±2 lm/W at 1000 cd/m2 for such deep-blue PHOLEDs with peak emission at a wavelength of 458 nm. [ABSTRACT FROM AUTHOR]

We have demonstrated that the light extraction efficiency of an organic light emitting device is a strong function of device geometry. Specifically, we have found that the ratio of the extracted mode to the substrate-guided mode varies from 22% to 55% depending on the location of the recombination zone. Our simulation results also indicate that more light is trapped in the substrate as the optical length of device increases. We further show that the light intensity profile varies from a Lambertian shape to a non-Lambertian shape depending on the device geometry due to the cavity effect. [ABSTRACT FROM AUTHOR]