Development of high performance OLEDs for general lighting
07 Feb 2013-Journal of Materials Chemistry C (The Royal Society of Chemistry)-Vol. 1, Iss: 9, pp 1699-1707
TL;DR: The first white organic light-emitting device (OLED) was developed in 1993, and the power efficiency and lifetime of this white OLED were reportedly only < 1 lm W−1 and < 1 day, respectively.
Abstract: Since the development of the first white organic light-emitting device (OLED) in 1993, twenty years have passed. The power efficiency and lifetime of this white OLED were reportedly only <1 lm W−1 and <1 day, respectively. However, recent rapid advances in material chemistry have enabled the use of white OLEDs for general lighting. In 2012, white OLED panel efficiency has reached 90 lm W−1 at 1000 cd m−2, and a tandem white OLED panel has realized a lifetime of over 100 000 hours. What is more important in OLEDs is to shed clear light on the new design products, such as transparent lighting panels and luminescent wallpapers. These fascinating features enable OLEDs as a whole new invention of artificial lighting. In this review, we would like to overview the recent developments of white OLED, especially three key elemental technologies related to material chemistry: (1) low operating voltage technology, (2) phosphorescent OLED technology and (3) multi-photon emission (MPE) device technology.
Citations
More filters
••
TL;DR: In this article, a perovskite solar cell was fabricated by using room-temperature deposition processes and the cells were based on a layer of methylammonium lead iodide perovsite that is prepared by sublimation in a high-vacuum chamber and sandwiched between two thin organic charge-transport layers.
Abstract: Highly efficient perovskite solar cells have been fabricated by using room-temperature deposition processes. The cells are based on a layer of methylammonium lead iodide perovskite that is prepared by sublimation in a high-vacuum chamber and sandwiched between two thin organic charge-transport layers.
1,318 citations
••
TL;DR: It is demonstrated that increasing the distance between donor (D) and acceptor (A) in intramolecular-charge-transfer molecules is a promising strategy for simultaneously achieving small ΔE(ST) and large k(F), which is in good agreement with those predicted by corrected time-dependent density functional theory.
Abstract: Red fluorescent molecules suffer from large, non-radiative internal conversion rates (kIC) governed by the energy gap law. To design efficient red thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diodes (OLEDs), a large fluorescence rate (kF) as well as a small energy difference between the lowest singlet and triplet excited states (ΔEST) is necessary. Herein, we demonstrated that increasing the distance between donor (D) and acceptor (A) in intramolecular-charge-transfer molecules is a promising strategy for simultaneously achieving small ΔEST and large kF. Four D-Ph-A-Ph-D-type molecules with an anthraquinone acceptor, phenyl (Ph) bridge, and various donors were designed, synthesized, and compared with corresponding D-A-D-type molecules. Yellow to red TADF was observed from all of them. The kF and ΔEST values determined from the measurements of quantum yield and lifetime of the fluorescence and TADF components are in good agreement with those predicted by corrected tim...
750 citations
••
TL;DR: In this article, the efficiency records of OLED devices using fluorescent, phosphorescent, and thermally activated delay fluorescent materials are summarized and a review of all the available efficiency-effective device architectural approaches, which include using thin layer structures, low carrier injection barriers, high carrier mobility, balanced carrier injection, effective carrier confinement, effective host-to-guest energy transfer, effective recombination zone, effective exciton generation on the host and p-i-n structures, and tandem structures.
Abstract: Efficiency is crucial for organic light emitting diodes (OLEDs) to be energy-saving and to have a long lifetime for display and solid state lighting applications. Numerous approaches have been proposed to attain high efficiency OLEDs through the synthesis of novel organic materials, the design of light extraction structures and the design of efficiency-effective device architectures. In this report, we first summarise the efficiency records of OLED devices using fluorescent, phosphorescent, and thermally activated delay fluorescent materials. Importantly, we review all the available efficiency-effective device architectural approaches, which include using thin layer structures, low carrier injection barriers, high carrier mobility, balanced carrier injection, effective carrier confinement, effective host-to-guest energy transfer, effective recombination zone, effective exciton generation on the host, effective exciton confinement, p–i–n structures, and tandem structures. It is hoped that better device structures can therefore be devised upon suitable device engineering to achieve higher efficiency for OLED devices.
507 citations
••
TL;DR: The recent advances in WPLEDs are summarized with special attention paid to the design of novel luminescent dopants and device structures that minimize the gap from other lighting sources such as fluorescent lamps, light-emitting diodes based on inorganic semiconductors, and vacuum-deposited small-molecular devices, thus rendering WPL EDs equally competitive.
Abstract: White polymer light-emitting devices (WPLEDs) have become a field of immense interest in both scientific and industrial communities. They have unique advantages such as low cost, light weight, ease of device fabrication, and large area manufacturing. Applications of WPLEDs for solid-state lighting are of special interest because about 20% of the generated electricity on the earth is consumed by lighting. To date, incandescent light bulbs (with a typical power efficiency of 12-17 lm W(-1) ) and fluorescent lamps (about 40-70 lm W(-1) ) are the most widely used lighting sources. However, incandescent light bulbs convert 90% of their consumed power into heat while fluorescent lamps contain a small but significant amount of toxic mercury in the tube, which complicates an environmentally friendly disposal. Remarkably, the device performances of WPLEDs have recently been demonstrated to be as efficient as those of fluorescent lamps. Here, we summarize the recent advances in WPLEDs with special attention paid to the design of novel luminescent dopants and device structures. Such advancements minimize the gap (for both efficiency and stability) from other lighting sources such as fluorescent lamps, light-emitting diodes based on inorganic semiconductors, and vacuum-deposited small-molecular devices, thus rendering WPLEDs equally competitive as these counterparts currently in use for illumination purposes.
451 citations
•
27 Mar 2015TL;DR: In this paper, novel tricarbazole compounds with appropriate HOMO and LUMO energies can be obtained for use as materials in a secondary hole transport layer, by appropriately selecting the nature of the tricarazole substituents.
Abstract: Novel tricarbazole compounds are provided. By appropriately selecting the nature of the tricarbazole substituents, compounds with appropriate HOMO and LUMO energies can be obtained for use as materials in a secondary hole transport layer.
445 citations
References
More filters
••
TL;DR: In this article, a double-layer structure of organic thin films was prepared by vapor deposition, and efficient injection of holes and electrons was provided from an indium-tinoxide anode and an alloyed Mg:Ag cathode.
Abstract: A novel electroluminescent device is constructed using organic materials as the emitting elements. The diode has a double‐layer structure of organic thin films, prepared by vapor deposition. Efficient injection of holes and electrons is provided from an indium‐tin‐oxide anode and an alloyed Mg:Ag cathode. Electron‐hole recombination and green electroluminescent emission are confined near the organic interface region. High external quantum efficiency (1% photon/electron), luminous efficiency (1.5 lm/W), and brightness (>1000 cd/m2) are achievable at a driving voltage below 10 V.
13,185 citations
••
TL;DR: In this paper, the performance of an organic light-emitting device employing the green electrophosphorescent material, fac tris(2-phenylpyridine) iridium [Ir(ppy)3] doped into a 4,4′-N,N′-dicarbazole-biphenyl host was described.
Abstract: We describe the performance of an organic light-emitting device employing the green electrophosphorescent material, fac tris(2-phenylpyridine) iridium [Ir(ppy)3] doped into a 4,4′-N,N′-dicarbazole-biphenyl host. These devices exhibit peak external quantum and power efficiencies of 8.0% (28 cd/A) and 31 lm/W, respectively. At 100 cd/m2, the external quantum and power efficiencies are 7.5% (26 cd/A) and 19 lm/W at an operating voltage of 4.3 V. This performance can be explained by efficient transfer of both singlet and triplet excited states in the host to Ir(ppy)3, leading to a high internal efficiency. In addition, the short phosphorescent decay time of Ir(ppy)3 (<1 μs) reduces saturation of the phosphor at high drive currents, yielding a peak luminance of 100 000 cd/m2.
3,594 citations
••
TL;DR: An improved OLED structure which reaches fluorescent tube efficiency and focuses on reducing energetic and ohmic losses that occur during electron–photon conversion, which could make white-light OLEDs, with their soft area light and high colour-rendering qualities, the light sources of choice for the future.
Abstract: The development of white organic light-emitting diodes (OLEDs) holds great promise for the production of highly efficient large-area light sources. High internal quantum efficiencies for the conversion of electrical energy to light have been realized. Nevertheless, the overall device power efficiencies are still considerably below the 60-70 lumens per watt of fluorescent tubes, which is the current benchmark for novel light sources. Although some reports about highly power-efficient white OLEDs exist, details about structure and the measurement conditions of these structures have not been fully disclosed: the highest power efficiency reported in the scientific literature is 44 lm W(-1) (ref. 7). Here we report an improved OLED structure which reaches fluorescent tube efficiency. By combining a carefully chosen emitter layer with high-refractive-index substrates, and using a periodic outcoupling structure, we achieve a device power efficiency of 90 lm W(-1) at 1,000 candelas per square metre. This efficiency has the potential to be raised to 124 lm W(-1) if the light outcoupling can be further improved. Besides approaching internal quantum efficiency values of one, we have also focused on reducing energetic and ohmic losses that occur during electron-photon conversion. We anticipate that our results will be a starting point for further research, leading to white OLEDs having efficiencies beyond 100 lm W(-1). This could make white-light OLEDs, with their soft area light and high colour-rendering qualities, the light sources of choice for the future.
3,095 citations
••
TL;DR: This device challenges incandescent sources by exhibiting total external quantum and power efficiencies that peak at 18.7 ± 0.6 lm W-1, respectively, and two distinct modes of energy transfer within this device serve to channel nearly all of the triplet energy to the phosphorescent dopants, retaining the singlet energy exclusively on the blue fluorescent dopant.
Abstract: Lighting accounts for approximately 22 per cent of the electricity consumed in buildings in the United States, with 40 per cent of that amount consumed by inefficient (approximately 15 lm W(-1)) incandescent lamps. This has generated increased interest in the use of white electroluminescent organic light-emitting devices, owing to their potential for significantly improved efficiency over incandescent sources combined with low-cost, high-throughput manufacturability. The most impressive characteristics of such devices reported to date have been achieved in all-phosphor-doped devices, which have the potential for 100 per cent internal quantum efficiency: the phosphorescent molecules harness the triplet excitons that constitute three-quarters of the bound electron-hole pairs that form during charge injection, and which (unlike the remaining singlet excitons) would otherwise recombine non-radiatively. Here we introduce a different device concept that exploits a blue fluorescent molecule in exchange for a phosphorescent dopant, in combination with green and red phosphor dopants, to yield high power efficiency and stable colour balance, while maintaining the potential for unity internal quantum efficiency. Two distinct modes of energy transfer within this device serve to channel nearly all of the triplet energy to the phosphorescent dopants, retaining the singlet energy exclusively on the blue fluorescent dopant. Additionally, eliminating the exchange energy loss to the blue fluorophore allows for roughly 20 per cent increased power efficiency compared to a fully phosphorescent device. Our device challenges incandescent sources by exhibiting total external quantum and power efficiencies that peak at 18.7 +/- 0.5 per cent and 37.6 +/- 0.6 lm W(-1), respectively, decreasing to 18.4 +/- 0.5 per cent and 23.8 +/- 0.5 lm W(-1) at a high luminance of 500 cd m(-2).
2,118 citations