Exciton quenching by diffusion of 2,3,5,6-tetrafluoro-7,7',8,8'-tetra cyano quino dimethane and its consequences on joule heating and lifetime of organic light-emitting diodes.
TL;DR: The effect of F(4)-TCNQ insertion at the anode/hole transport layer (HTL) interface was studied on joule heating and the lifetime of organic light-emitting diodes (OLEDs).
Abstract: In this Letter, the effect of F4-TCNQ insertion at the anode/hole transport layer (HTL) interface was studied on joule heating and the lifetime of organic light-emitting diodes (OLEDs). Joule heating was found to reduce significantly (pixel temperature decrease by about 10 K at a current density of 40 mA/cm2) by this insertion. However, the lifetime was found to reduce significantly with a 1 nm thick F4-TCNQ layer, and it improved by increasing the thickness of this layer. Thermal diffusion of F4-TCNQ into HTL leads to F4-TCNQ ionization by charge transfer, and drift of these molecules into the emissive layer caused faster degradation of the OLEDs. This drift was found to reduce with an increase in the thickness of F4-TCNQ.
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TL;DR: The theme of this report, summarizing the knowledge of mechanisms allied with OLED degradation, would be contributory in developing better‐quality OLED materials and, accordingly, longer lifespan devices.
Abstract: Organic light emitting diodes (OLEDs) have been well known for their potential usage in the lighting and display industry. The device efficiency and lifetime have improved considerably in the last three decades. However, for commercial applications, operational lifetime still lies as one of the looming challenges. In this review paper, an in-depth description of the various factors which affect OLED lifetime, and the related solutions is attempted to be consolidated. Notably, all the known intrinsic and extrinsic degradation phenomena and failure mechanisms, which include the presence of dark spot, high heat during device operation, substrate fracture, downgrading luminance, moisture attack, oxidation, corrosion, electron induced migrations, photochemical degradation, electrochemical degradation, electric breakdown, thermomechanical failures, thermal breakdown/degradation, and presence of impurities within the materials and evaporator chamber are reviewed. Light is also shed on the materials and device structures which are developed in order to obtain along with developed materials and device structures to obtain stable devices. It is believed that the theme of this report, summarizing the knowledge of mechanisms allied with OLED degradation, would be contributory in developing better-quality OLED materials and, accordingly, longer lifespan devices.
104 citations
TL;DR: In this paper, the electron transport enhancing diphenyl phosphine-oxide (Ph2PO) group has been added to blue light emitting pyrene derivatives to obtain highly efficient electron transporting blue-emitters for non-doped organic light emitting devices (OLEDs) with good film formation characteristics.
Abstract: In a search for blue light emitting multifunctional materials, the electron transport enhancing diphenyl phosphine–oxide (Ph2PO) group has been appended to blue light emitting pyrene derivatives. This design, we observe, leads to highly efficient electron transporting blue-emitters for non-doped organic light emitting devices (OLEDs) with good film formation characteristics. The superior performance is attributed to enhanced charge transport and formation of pyrene excimers assisted by thermally activated delayed fluorescence (TADF) in the device. We report the synthesis and characterization using experimental and computational methods of six such pyrene derivatives. Although three of these derivatives show quenching of luminescence in solvents at higher concentrations, in the thin film invariably all six of them exhibit typical pyrene excimer emission. X-ray crystal analysis reveals π–π stacking and the C–H⋯O interactions in the solid due to the PO group. The measured electron mobilities for all the compounds are higher in comparison to the standard electron transport material, Alq3. Non-doped OLEDs with the pyrene derivatives as emitters (multi-layer configuration) as well as electron transport cum emitters (bilayer configuration) exhibit excellent efficiencies. The derivatives as emitters display a performance with current efficiencies (ηc) in the range 21.1–30.1 cd A−1, power efficiencies (ηp) 11.0–15.76 lm W−1, external quantum efficiencies (EQE) 7.2–9.1% and brightness 28 500–42 750 cd m−2. In addition, the derivatives as electron transporting emitters demonstrate very good external quantum efficiencies in the range of 3.0–4.0%. These results demonstrate a successful strategy to obtain blue light emitting multifunctional materials for OLED applications.
78 citations
TL;DR: In this article, the authors reported two new phenanthroline-based compounds, 1,4-bis(2-phenyl-1,10-phenanthrolin-4-yl)benzene (p-bPPhenB) and 1,3-bis (2-PNyl- 1,10phenanthuslin- 4-yl), for the charge generation unit of tandem organic light-emitting diodes (OLEDs).
Abstract: In this paper, we report two new phenanthroline-based compounds, 1,4-bis(2-phenyl-1,10-phenanthrolin-4-yl)benzene (p-bPPhenB) and 1,3-bis(2-phenyl-1,10-phenanthrolin-4-yl)benzene (m-bPPhenB), for the charge generation unit of tandem organic light-emitting diodes (OLEDs). These two compounds exhibited high electron mobility of (5.8–4.4) × 10–3 cm2/(V s), a very small injection barrier at the p–n junction interface, a high glass transition temperature of 123.9–182.1 °C, and exceptionally good operational stability. Because of such excellent characteristics, a single-stack red phosphorescent OLED (PhOLED) with p-bPPhenB showed a low driving voltage (2.7 V) and significantly improved maximum power efficiency (56.8 lm/W), external quantum efficiency (30.8%), and device lifetime (LT95, 130 h) compared to those of the control device using bathophenanthroline (Bphen) (3.7 V, 39 lm/W, 27.1%, and 13 h). Furthermore, a two-stack (tandem) red PhOLED using p-bPPhenB in the charge generation unit exhibited superior cha...
63 citations
TL;DR: In this article, a series of 2′,6′-difluoro-2,3′-bipyridine cyclometalating ligands were synthesized by substituting electron-withdrawing (CHO, CF3, and CN) and electron-donating (OMe and NMe2) groups at the 4′ position of the pyridyl moiety and utilized them for the construction of five new iridium(III) complexes.
Abstract: Herein, we have synthesized a series of 2′,6′-difluoro-2,3′-bipyridine cyclometalating ligands by substituting electron-withdrawing (–CHO, –CF3, and –CN) and electron-donating (–OMe and –NMe2) groups at the 4′ position of the pyridyl moiety and utilized them for the construction of five new iridium(III) complexes (Ir1–Ir5) in the presence of picolinate as an ancillary ligand. The photophysical properties of the developed iridium(III) compounds were investigated with a view to understand the substituent effects. The strong electron-withdrawing (–CN) group containing the iridium(III) compound (Ir3) exhibits highly efficient genuine green phosphorescence (λmax = 508 nm) at room temperature in solution and in thin film, with an excellent quantum efficiency (ΦPL) of 0.90 and 0.98, respectively. On the other hand, the –CF3 group substituted iridium(III) compound (Ir2) displays a sky-blue emission (λmax = 468 nm) with a promising quantum efficiency (ΦPL = 0.88 and 0.84 in solution and in thin film, respectively). The –CHO substituted iridium(III) complex (Ir1) showed greenish-yellow emission (λmax = 542 nm). Most importantly, the strong electron-donating –NMe2 substituted iridium(III) complex (Ir5) gives a structureless and a broad emission profile in the wavelength region 450 to 700 nm (λmax = 520 nm) with a poor quantum efficiency. An intense blue phosphorescence with impressive quantum efficiency, especially in thin-film noted in the case of the –OMe substituted iridium(III) complex (Ir4). Comprehensive density functional theory (DFT) and time-dependent DFT (TD-DFT) approaches have been performed on the ground and excited states of the synthesized iridium(III) complexes, in order to obtain information about the absorption and emission processes and to gain deeper insights into the photophysical properties. The combinations of a smaller ΔES1–T1 and higher contribution of 3MLCT in the emission process result in the higher quantum yields and lifetime values for complexes Ir1–Ir3. Multi-layered Phosphorescent Organic Light Emitting Diodes (PhOLEDs) were designed using the phosphorescent dopants Ir2, Ir3 and Ir4 and their elecroluminescence properties were evaluated. Compound Ir4 at a doping level of 5 wt% shows the best performance with an external quantum efficiency of 4.7%, in the nonoptimized device, and a power efficiency of 5.8 lm W−1, together with a true-blue chromacity CIEx,y = 0.15, 0.17 recorded at the maximum brightness of 33180 cd m−2.
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References
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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: In this article, an ultrathin LiF layer adjacent to an electron-transporting layer and an aluminum outerlayer was used as an electrode for organic electroluminescent devices.
Abstract: A bilayer is used as an electrode for organic electroluminescent devices The bilayer consists of an ultrathin LiF layer adjacent to an electron-transporting layer and an aluminum outerlayer Devices with the bilayer electrode showed enhanced electron injection and high electroluminescence efficiency as compared with a Mg09Ag01 cathode Similar effects were observed when replacing MgO for LiF The improvements are attributed to band bending of the organic layer in contact with the dielectrics
1,471 citations
TL;DR: Most present-day semiconductor devices use inorganic crystalline materials, with single-crystalline silicon dominating other materials like GaAs by about a factor of 1000, but organic semiconductors have recently gained much attention and are already broadly applied as photoconductors for copiers and laser printers.
Abstract: Most present-day semiconductor devices use inorganic crystalline materials, with single-crystalline silicon dominating other materials like GaAs by about a factor of 1000. Despite the advantages of single-crystalline inorganic semiconductors like high room-temperature mobility (up to 1000 cm2/(V s)) and high stability, these materials are less suitable for low-cost and large-area applications. Additionally, silicon is an indirect semiconductor and therefore is not well suited for optoelectronic applications like light-emitting diodes. Solar cells from silicon are expensive and require a large amount of energy for their fabrication, leading to a long energy payback time. As an alternative, organic semiconductors have recently gained much attention (for review articles, see refs 1 -3 (OLEDs), ref 4 (organic electronics in general), and refs 5 and 6 (organic solar cells)). Originally, much of the research concentrated on single crystals, which can have mobilities of a few cm2/(V s) at room temperature and even much higher values at low temperature, as shown in the pioneering work of Karl et al.7 However, for practical applications, thinfilm organic semiconductors with disordered morphology, such as evaporated small-molecule compounds or polymers processed from solution, are prevailing. Organic semiconductors are already broadly applied as photoconductors for copiers and laser printers. * Corresponding author. E-mail: leo@iapp.de. Web address: www.iapp.de. 1233 Chem. Rev. 2007, 107, 1233−1271
1,436 citations
TL;DR: The types of materials (small molecules and polymers) that have been used to fabricate WOLEDs are described and a range of device architectures are presented and appraised.
Abstract: WOLEDs offer new design opportunities in practical solid-state lighting and could play a significant role in reducing global energy consumption. Obtaining white light from organic LEDs is a considerable challenge. Alongside the development of new materials with improved color stability and balanced charge transport properties, major issues involve the fabrication of large-area devices and the development of low-cost manufacturing technology. This Review will describe the types of materials (small molecules and polymers) that have been used to fabricate WOLEDs. A range of device architectures are presented and appraised.
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