High-efficiency organic light-emitting diodes based on ultrathin blue phosphorescent modification layer

Yellow organic light-emitting devices(YOLEDs) with a novel structure of ITO/MoO_3(5 nm)/NPB(40 nm)/TCTA(15 nm)/CBP:(tbt)_2Ir(acac)(x%)(25 nm)/FIrpic(y nm)/TPBi(35 nm)/Mg:Ag are fabricated. The ultrathin blue phosphorescent bis[(4,6-difluorophenyl)-pyridi-nato-N,C2■](picolinate) iridium(Ⅲ)(FIrpic) layer is regarded as a highperformance modification layer. By adjusting the thickness of FIrpic and the concentration of (tbt)_2Ir(acac), a YOLED achieves a high luminance of 41618 cd/m~2, power efficiency of 49.7 lm/W, current efficiency of 67.3 cd/A, external quantum efficiency(EQE) of 18%, and a low efficiency roll-off at high luminance. The results show that phosphorescent material of FIrpic plays a significant role in improving YOLED performance. The ultrathin FIrpic modification layer blocks excitons in EML. In the meantime, the high triplet energy of FIrpic(2.75 eV) alleviates the exciton energy transport from EML to FIrpic.     

Non-doped phosphorescent white organic light-emitting devices with a quadruple-quantum-well structure

Non-doped white organic light-emitting devices (WOLEDs) with a quadruple-quantum-well structure were fabricated. An alternate layer of ultrathin blue and yellow iridium complexes was employed as the potential well layer, while potential barrier layers (PBLs) were chosen to be 2,2',2''-(1,3,5-benzenetriyl)-tris(1-phenyl-1-H-benzimidazole) (TPBi) or N,N'-dicarbazolyl-3,5-benzene (mCP) combined TPBi. On adjusting the PBLs for device performance comparison, the results showed that the device with all-TPBi PBLs exhibited a yellow emission with the color coordinates of (0.50,0.47) at a luminance of 1000 cd/m², while stable white emission with the color coordinates of (0.36,0.44) was observed in the device using mCP combined TPBi as the PBLs. Meanwhile, for the WOLED, with a reduced efficiency roll-off, a maximum luminance, luminous efficiency, and external quantum efficiency of 12,610 cd/m², 10.2 cd/A, and 4.4%, respectively, were achieved. The performance improvement by the introduction of mCP PBL was ascribed to the well confined exciton and the reduced exciton quenching effect in the multiple emission regions.     

Effect of various red phosphorescent dopants in single emissive white phosphorescent organic light-emitting devices

In order to realize single emissive white phosphorescent organic light-emitting devices(PHOLEDs) with three color phosphorescent dopants(red, green, and blue), the energy transfer between the host material and the three dopants, as well as the among the three dopants themselves, should be considered and optimized. To explore the effect of red phosphorescent dopant on the color rendering index(CRI), the authors investigate the wavelength position of the maximum emission peak from three phosphorescent dopants. The CRI and luminous efficiency of white PHOLED in which Ir(pq)_2(αcαc) acts as the red phosphorescent dopant are found to be greater than those of devices prepared using Ir(pig)_3 and Ir(pq)_2(αcαc) as the emission spectrum has a relatively high intensity near the human perception of blue, red, and green wavelengths. Furthermore, we demonstrate that the performance of the three dopants is related to the absorption characteristics of the red phosphorescent dopant.With a maximum emission peak at 600 nm, Ir(pq)_2(αcαc) has a higher intensity in the concave section between 550 and 600 nm seen for red and blue dopants. In addition, the long metal-to-ligand charge transfer(MLCT)absorption tail of Ir(pq)_2(αcαc) overlaps with the emission spectra of the green dopant, enhancing emission. Such energy transfer mechanisms are confirmed to optimize white emission in the single emissive white PHOLEDs.     

Recombination zone shift in phosphorescent white organic light-emitting devices with single host structure of multi-emission layers

We have investigated the recombination zone in the phosphorescent white organic light-emitting devices with single host structure of multi-emission layers. Blue, green, and orange-red phosphorescent emitters were doped into the separate layers of single host material for fabricating the white devices with multi-emission layers. The electroluminescence spectrum was substantially modified by the shift of the recombination zone that was dependent upon the thickness of the electron transport layer. We investigated the recombination zone shift in terms of electric field distribution and carrier injection. A maximum external quantum efficiency of 15.9% and a maximum power efficiency of 28.9 lm/W were achieved by optimizing the recombination zone.     

High power efficiency in single layer blue phosphorescent organic light-emitting diodes

High efficiency single layer blue phosphorescent organic light-emitting diodes (PHOLEDs) without any charge transport layer were developed. A mixed host of spirobifluorene based phosphine oxide (SPPO13) and 1, 1-bis[(di-4-tolylamino)phenyl]cyclohexane (TAPC) was used as the host in the emitting layer. A high maximum external quantum efficiency of 15.8% and a quantum efficiency of 8.6% at 1000 cd/m² were achieved in the single-layer blue PHOLEDs without any charge transport layer. The maximum power efficiency and power efficiency at 1000 cd/m² were 31.4 and 16.9 lm/W, respectively.     

High efficiency blue phosphorescent organic light-emitting diodes without electron transport layer

High efficiency blue phosphorescent organic light-emitting diodes were fabricated without an electron transport layer using a spirobifluorene based blue triplet host material. The simple blue PHOLEDs without the electron transport layer showed a high external quantum efficiency and current efficiency of 16.1% and 30.2 cd/A, respectively. The high device performances of the electron transport layer free blue PHOLEDs were comparable to those of blue PHOLEDs with the electron transport layer.     

Efficient white organic light-emitting diodes based on an orange iridium phosphorescent complex

Stable and efficient white light emission is obtained by mixing blue fluorescence and orange phosphorescence. The introduction of double exciton blocking layers brings about well confinement of both charge-carriers and excitons in the emission layer. By systematically adjusting blue fluorescent and orange phosphorescent emission layers thickness, carriers in emission zone are balanced, and electrically generated excitons can be efficiently utilized. One white device with power efficiency of 14.4 lm/W at 100 cd/m² has excellently stable spectra. The improvement of performance is attributed to efficient utilization of the excitons and more balance of charge-carriers in emission layer.     

Solution-processed white organic light-emitting devices based on small-molecule materials

We investigated solution-processed films of 4,4′-bis(2,2-diphenylvinyl)-1,1′-bibenyl (DPVBi) and its blends with N,N′-bis(3-methylphenyl)-(1,1′-biphenyl)-4,4′-diamine (TPD) by atomic force microscopy (AFM). The AFM result shows that the solution-processed films are pin-free and their morphology is smooth enough to be used in OLEDs. We have developed a solution-processed white organic light-emitting device (WOLEDs) based on small-molecules, in which the light-emitting layer (EML) was formed by spin-coating the solution of small-molecules on top of the solution-processed hole-transporting layer. This WOLEDs, in which the EML consists of co-host (DPVBi and TPD), the blue dopant (4,4′-bis[2-(4-(N,N-diphenylamino)phenyl)vinyl]biphenyl) and the yellow dye (5,6,11,12-tetraphenylnaphtacene), has a current efficiency of 6.0 cd/A at a practical luminance of 1000 cd/m², a maximum luminance of 22500 cd/m², and its color coordinates are quite stable. Our research shows a possible approach to achieve efficient and low-cost small-molecule-based WOLEDs, which avoids the complexities of the co-evaporation process of multiple dopants and host materials in vacuum depositions.     

利用BCP层调节白色磷光有机电致发光器件色度的研究

制备了三种结构的白色有机电致发光器件，通过比较得出：在发光层中间插入2，9-二甲基-4，7-二苯基-1，10-菲咯啉(BCP)能有效控制载流子在不同发光层的分布，进而对器件色度进行调节；而掺杂磷光染料Ir(ppy)₃作敏化剂能有效提高器件的效率. 结构为:氧化铟锡/聚乙烯基咔唑∶N，N′-二(1-萘基)-N，N′-二苯基-1，1′-联苯-4-4′-二胺(30nm)/二-(2-甲基-8-羟基喹啉)-4-联苯酚铝：3.0 wt%2，5，8，11-tetra-tertbutylperylene(TBPe)(30nm)/BCP(5.0nm)/4,4N,N二咔唑基二苯：5.0 wt%Ir(ppy)₃:2.0 wt%红荧烯(15nm)/BCP(10nm)/Mg:Ag的器件色度和效率俱佳. 其在17V工作电压下具有的亮度为4670cd/m²，对应色坐标为(0.31,0.37). 器件具有的最大外量子效率为1.4%，当驱动电压从5.0V升高到17V，器件色坐标严格位于白光色域区内. 关键词： 磷光染料 阻挡层 白光 双发光层     

Highly efficient all phosphorescent white organic light-emitting diodes for solid state lighting applications

We report highly efficient all phosphorescent white organic light-emitting diodes (OLEDs) with an exciton-confinement structure. By stacking two emissive layers (EMLs) with different charge transporting properties, effective charges as well as exciton confinements were achieved. Accordingly, efficient blue OLEDs with a peak external quantum efficiency (EQE) over 22% and power efficacy (PE) over 50 lm/W were developed by using iridium(III) bis(4,6-(difluorophenyl) pyridinato-N,C2′)picolinate (FIrpic) as an electro-phosphorescent dopant. When the optimized orange and red EMLs were sandwiched between the stacked two blue EMLs, white OLEDs with an EQE and PE of 24.3% and 45.9 lm/W at a luminance of 1000 cd/m² were obtained without the use of any out-coupling techniques. In addition, these white OLEDs exhibit a color rendering index (CRI) value of 84 with high efficacy.     

Effect of gold nanoparticles on the performances of the phosphorescent organic light-emitting devices

Gold nanoparticles (GNPs) on the performance of the phosphorescent organic light-emitting devices (OLEDs) were investigated. The green phosphorescent OLEDs with GNPs incorporated in hole transporting layer (HTL) or hole blocking layer (HBL) were fabricated using thermal evaporation technique. The results indicated that the performance of the OLEDs with GNPs were dependent on the position of the GNPs. The optimized device with GNPs in HBL shows enhanced current efficiency and reduced efficiency roll-off. However, the efficiency of the device with GNPs in HTL was decreased. The detailed physical mechanism is investigated in order to unveil such difference.     

Angle-stable top-emitting white organic light-emitting devices employing a down-conversion layer

Angle-stable white top-emitting organic light-emitting devices (WTEOLEDs) by the combination of a blue TEOLED with a down-conversion (DC) layer are demonstrated. The DC layer is composed of red fluorescent dye doped in a host of tris (8-hydroxy-quinolinato) aluminum. The TEWOLED shows a CIE coordinates of (0.240, 0.332) and a maximum current efficiency of 3.95 cd/A. Furthermore, the WTEOLED shows excellently angle-stable characteristic, the CIE coordinates at 20 mA/cm² only shift by (0.023, −0.007) from 0° to 60°. It can be attributed to the angle-stable blue TEOLED based on the Ag/Ge/Ag transparent cathode.     

Efficiency improvement of red organic light-emitting diodes using a blue phosphorescent exciton blocking layer

Quantum efficiency of red organic light-emitting diodes was improved using a blue phosphorescent emitting layer as an exciton blocking layer. Compared with 8.1% quantum efficiency of standard devices without an exciton blocking layer, high quantum efficiency of 14.1% was obtained using a blue phosphorescent emitting layer between the hole transport layer and the red emitting layer.     

Fabrication of blue top-emitting organic light-emitting devices with highly saturated color

Blue top-emitting organic light-emitting devices (TOLEDs) with highly saturated color were developed by microcavity effect. The device structure studied was glass/reflective silver/indium-tin oxide (ITO)/organic electroluminescent stack/semi-transparent cathode (calcium/silver). By changing the thicknesses of ITO and organic layers in the microcavity structure device doped with p-bis(p-N, N-di-phenyl-aminostyryl)benzene (DSA-ph), highly saturated color with Commission Internationale de L'Eclairage chromaticity coordinates (CIE_x,y) of (0.14, 0.08) was obtained.     

Luminescence mechanisms of green and blue organic light-emitting devices utilizing hole-blocking layers

Optical and electrical measurements on green and blue organic light-emitting devices (OLEDs) with and without hole-blocking layers (HBLs) were performed, and the luminescence mechanisms of green and blue OLEDs utilizing HBLs were investigated by using energy band diagrams and carrier density distributions. The dependence of the electroluminescence efficiencies on the existence of HBLs was described on the basis of a luminescence mechanism. The density distributions of the electrons and the holes in OLEDs under applied electric fields were estimated from the energy band diagrams, taking into account the electronic parameters and the layer thicknesses. The luminescence efficiencies and the color chromaticities were significantly affected by the existence of the HBLs. These analyses can help improve understanding of the luminescence mechanisms at play in and the electroluminescence efficiencies of green and blue OLEDs with HBLs, and the present results provide important information on the optical properties for enhancing the efficiencies of OLEDs operating in the green and the blue regions of the spectra.     

Efficient fluorescent white organic light-emitting devices with a reduced efficiency roll-off based on a blue ambipolar fluorescent emitter

White organic light-emitting devices (WOLEDs) with fluorescent donor-acceptor-substituted spirobifluorene compounds (red 2-diphenylamino-7-(2,2-dicyanovinyl)-9,9′-spirobifluorene and blue 2-diphenylamino-7-(2,2-diphenylvinyl)-9,9′-spirobifluorene) have been fabricated. The optimized WOLEDs shows a maximum current efficiency 5.9 cd/A and very low efficiency roll-off. From the brightness at maximum current efficiency to high brightness of 10000 cd/m², the current efficiency roll-off is only 0.4%. It can be attributed to the ambipolar blue fluorescent emitter with voltage-independnet mobility which makes the device having a broader charge recombination zone and balance of carrier transport.     

White organic light-emitting devices

In view of their potential applications in flat panel displays, organic light-emitting devices have attracted much attention in the past decade. A challenging target in this field is to realize full color display applications. One of the approaches proposed for these is combining white emission with color filters, where efficient and pure white emission (especially at high brightness) is necessary. In this paper, three kinds of white organic light-emitting devices with different structures and materials are fabricated and their characteristics are discussed.     

High-external-quantum-efficiency organic light-emitting devices

We study the internal and external quantum efficiencies of vacuum-deposited organic light-emitting devices (OLED's). The internal quantum efficiency of OLED's based on tris-(8-hydroxyquinoline) aluminum is calculated to be 5.7 times the observed external quantum efficiency ?(e), consistent with measurements. We demonstrate a shaped substrate that increases ?(e) by a factor of 1.9+/-0.2 over similar OLED's fabricated upon flat glass substrates and leads to a 100%-emissive aperture, i.e., the emitting area completely occupies the display area even in the presence of metal interconnects. We also discuss a substrate structure that increases ?(e) by an additional factor of 2. The high device efficiencies are promising for developing OLED-based displays with extremely low power consumption and increased operational lifetime.     

Co50Fe50-xSix合金的结构相变和磁性

利用实验测量和理论计算相结合的方法,研究了介于B2结构CoFe低有序合金和L2₁结构Co₂FeSi高有序合金之间的Co₅₀Fe_50-xSi_x合金的结构相变、磁相变、分子磁矩和居里温度.采用考虑Coulomb相互作用的广义梯度近似(GGA+U)方法计算了合金的能带结构.研究发现,合金出现较强的原子有序倾向,表现出较强的共价成相作用.合金的晶格常数、磁矩、居里温度随Si含量的增加而线性地降低,极限成分Co₂FeSi合金的分子磁矩和居里温度分别达到5.92μ_B和777 ℃.原子尺寸效应导致合金晶格发生变化,但并未成为居里温度和分子磁矩变化的主导因素.分子磁矩的变化符合Slater-Pauling原理,但发现原子磁矩的变化并非线性,据此提出了共价成相对磁性影响的观点.采用Stearns理论解释了居里温度的变化趋势,排除了原子间距对居里温度的主导影响作用.能带计算的结果还表明,Co₂FeSi作为半金属材料并非十分完美,可能在实际应用中会出现自旋极化率降低的问题.发现该系列合金的结构相变和磁相变随着成分的变化聚集在窄小的成分和温度范围内. 关键词： 磁性 Heusler合金 结构相变     

Ca/Ag bilayer cathode for transparent white organic light-emitting devices

We have demonstrated that the compositional modification of the Ca/Ag films is principally responsible for a high transmittance (over 70% in the visible range) and low sheet resistance (10-12 Ω/sq). X-ray photoelectron spectroscopy (XPS) sputter depth profiling of Ca/Ag structure reveals the presence of Ca(OH)₂ and Ca metal. A chemical model of the Ca/Ag cathode is proposed. Using transparent ITO anode and Ca (10 nm)/Ag (10 nm) cathode, efficient white organic light-emitting devices (WOLEDs) emitting from both sides have been fabricated. Brightness of 3813 cd/m² and Commission Internationale de l’Eclairage (CIE) coordinates (0.36, 0.34) at 10 V through ITO anode and values of 1216 cd/m² and (0.33, 0.30) through Ca/Ag cathode are reported. A low turn-on voltage of 5.5 V is measured.