Performance Of Organic Light-emitting Diodes Research Articles

TiO2-Nanobelt-Enhanced, Phosphorescent, Organic Light-Emitting Diodes

This study investigates the enhancement of organic light-emitting diode (OLED) performance through the integration of titanium dioxide (TiO2) nanocomposites within a poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT/PSS) matrix. The nanocomposite films were prepared using a controlled dispersion of TiO2 belts into the PEDOT/PSS solution, followed by their incorporation into the OLED hole-injection layer (HIL). Our results demonstrate a significant improvement in device efficiency, attributed to the optimized charge carrier mobility and reduced recombination losses, which were achieved by the presence of TiO2. The nanocomposite hybrid layer enhances light emission efficiency due to its role in modifying surface roughness, promoting better film uniformity, and improving hole injection. The incorporation of TiO2 nanobelts into PEDOT/PSS led to significant efficiency enhancements, yielding a 39% increase in PEmax, a 37% improvement in CEmax, and a remarkable 72% rise in EQEmax compared to the undoped counterpart. This research provides insight into the potential of TiO2 nanocomposites in advancing OLED technology for next-generation display and lighting applications.

Toward High-Performance Pure-Green Tandem Organic Light-Emitting Diodes by Employing Barrier-Free Strategies in the Charge Generation Layer.

Charge generation layers (CGLs) play crucial roles in determining the electroluminescence (EL) performance of tandem organic light-emitting diodes (OLEDs). However, acquiring negligible voltage drops across the CGL unit and high-efficiency multiplications remains challenging. Here, we propose barrier-free strategies to compose a high-performance p-i-n type CGL intermediate by introducing a Yb/HI-9 modification at the heterojunction and a novel n-dopant, Yb:1,3-bis(9-phenyl-1,10-phenanthrolin-2-yl)benzene (mdPPhen), as the n-CGL. Mechanism analysis confirms that the Yb/HI-9 modification efficiently eliminates the intrinsic energy mismatch at the n-CGL/p-CGL interface, while the lowest unoccupied molecular orbital (LUMO) of the n-dopant can be aligned to the electron transport layer of adjacent EL units, creating improved electron transport. Consequently, the resulting 2-EL unit tandem OLEDs exhibited no voltage drops across the CGL intermediate with excellent efficiency multiplications. Notably, the barrier-free CGL strategy worked efficiently in the sensitized fluorescence tandem OLED with low operating voltage, extremely high efficiency (current efficiency of 267.2 cd/A, external quantum efficiency of 62.6%), and operational stability (95% of the initial luminance at 3000 cd/m2, T95 of 4713 h) with pure-green emission (CIEy coordinate of over 0.68), showing the best tandem OLED among reported CGLs to satisfy commercial demands.

Deep Blue Emitter with a Combination of Hybridized Local and Charge Transfer Excited State and Aggregation-Induced Emission Features for Efficient Non-Doped OLED.

Herein, a deep blue emitter (PI-TPB-CN) with a synergistic effect of hybridized local and charge transfer excited state (HLCT) and aggregation-induced emission (AIE) properties is successfully designed and synthesized to improve the performance of deep blue organic light-emitting diodes (OLEDs). It is constructed using a 1,2,4,5-tetraphenylbenzene (TPB) as an π-conjugated AIE core being asymmetrically functionalized with a phenanthro[9,10-d]imidazole (PI) as a weak donor (D) and a benzonitrile (CN) as an acceptor (A), thereby formulating D-π-A type fluorophore. Its HLCT and AIE properties verified by theoretical calculations, solvatochromic effects, and transient photoluminescence decay experiments, bring about a strong blue emission (452 nm) with a high photoluminescence quantum yield of 74 % in the thin film. PI-TPB-CN is successfully employed as a blue emitter in OLEDs. Non-doped OLED with the structure of ITO/HAT-CN (6 nm)/NPB (30 nm)/TCTA (10 nm)/PI-TPB-CN (30 nm)/TPBi (40 nm)/LiF (1 nm)/Al (100 nm) demonstrates excellent electroluminescence (EL) performance with blue emission (451 nm) and maximum external quantum efficiency (EQEmax) of 7.38 %. The device with a thinner layer of PI-TPB-CN (20 nm) and TPBi (30 nm) exhibits a deeper blue emission (444 nm) with CIE coordinates of (0.156, 0.096), a low turn-on voltage of 3.0 V, and EQEmax of 6.45 %.

Enhanced performance of solution-processed organic light-emitting diodes with TEMPOL derivatives

This study reports novel solution-processed 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL)-derivative organic compounds in a widely employed hole-injection/transport poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) layer. The TEMPOL-derived organic dopants, synthesized via a one-step chemical procedure, exhibited distinctive molecular dipole characteristics and electrical conductivities. The green organic light-emitting diodes (OLEDs) with a 4-benzene sulfonyl-2,2,6,6-tetramethyl-1-piperidenyloxy radical (TBS)-doped PEDOT:PSS layer exhibited a maximum power efficiency (PEmax) of 25.58 lm W−1, maximum external quantum efficiency (EQEmax) of 12.19 %, and maximum current efficiency (CEmax) of 40.85 cd A−1, demonstrating significant improvements compared with the pristine PEDOT:PSS layer-based device. The PEmax (16.18 lm W−1), EQEmax (10.67 %), and CEmax (37.01 cd A−1) were obtained with fiber OLEDs under same conditions. This enhancement in OLED performance can be attributed to the decreased hole-injection barrier at the anode and emissive layer interfaces.

Unveiling the ligand effects on Pt(Ⅱ) carbene complexes for rapid, efficient and narrow-spectra blue phosphorescence

Tetradentate Pt(II) complexes, comprising of benzoimidazolyl N-heterocyclic carbene (BI-NHC) coordination, have shown superior performance in blue phosphorescent organic light-emitting diodes (PhOLEDs). Here, four frame-structured complexes were synthesized to explore the intrinsic ligand effect for rapid, efficient and narrow-spectra blue phosphorescence through experimental analyses and theoretical calculations. We found carbazolylpridine (CzPy) chelating part in Pt(II) BI-NHC complexes dominates the phosphorescence with the suppression of metal-centered transition and electron-vibration coupling. Consequently, the CzPy chelated complexes (PtN-dip and PtN-dtb) achieved high luminescent efficiency, rapid radiative decay rate (kr) and narrow emission spectra. The peripheral substituent 2,6-di-iso-propylphenyl (dip) on NHC of PtN-dip constrains the molecule, significantly reducing the non-radiative decay rate (knr) and enhancing the efficiency. The 3,5-di-tert-butylphenyl (dtb) in PtN-dtb could enhances low-frequency vibration coupling that could expedite the excitons decay, resulting in higher kr and knr. This work unveils the intrinsic factors behind the ligand effects of Pt(II) BI-NHC based complexes, leading to a rapid, efficient and narrow-spectra phosphorescence.

Rational Molecular Design of Phenanthroimidazole-Based Fluorescent Materials toward High-Efficiency Deep-Blue OLEDs by Molecular Isomer Engineering.

Organic light-emitting diodes (OLEDs) have been extensively investigated in full-color displays and energy-saving lighting owing to their unique advantages. However, deep-blue OLEDs based on nondoped emitting layers with a satisfactory external quantum efficiency (EQE) are still rare for applications. In this work, six hot exciton materials, PPIM-12F, PPIM-22F, PPIM-13F, PPIM-23F, PPIM-1CN, and PPIM-2CN, are designed and synthesized via an isomer engineering design strategy and their photophysical properties and OLED performance are systematically investigated. These emitters all possess wide band gaps (3.53-3.69 eV), hybrid local and charge transfer (HLCT) characteristics, and good thermal stabilities. The C2 series compounds, PPIM-22F, PPIM-23F, and PPIM-2CN, all show redder emission peaks than the N1 series counterparts of PPIM-12F, PPIM-13F, and PPIM-1CN. In addition, the LUMO energy levels decrease consecutively in the sequence of PPIM-22F < PPIM-23F < PPIM-2CN and are all lower than their respective N1 series position isomers of PPIM-12F, PPIM-13F, and PPIM-1CN. The CV measurements indicate that such a design strategy renders the fine-tuning of LUMO energy levels, and the incorporation of electron acceptors at the extended C2 position of the PI unit is a better choice to improve the electron injection ability. Theoretical simulations indicate that they may harvest the triplet exciton through an upper-level reverse intersystem crossing process, which decreases the gathering of triplet excitons and allows the OLEDs to be fabricated by nondoping technology. Among them, PPIM-22F with a difluorobenzene substituent at the C2 position manifests the best performance in OLEDs, which exhibits the maximum EQE of 7.87% and Commission Internationale de ĺEclairage (CIE) coordinates of (0.16, 0.10). This work demonstrates an effective strategy for considerable improvement in device performance by a subtle change in the molecular structure through isomer engineering.

Optical Properties and Growth Characteristics of 8-Quinolinolato Lithium (Liq) Nano-Layers Deposited by Gas Transport Deposition.

Organometallic complexes containing reactive alkali metals, such as lithium (Li), represent a promising material approach for electron injection layers and electron transport layers (EILs and ETLs) to enhance the performance of Organic Light-Emitting Diodes (OLEDs). 8-Quinolinolato Lithium (Liq) has shown remarkable potential as an EIL and ETL when conveyed in very thin films. Nevertheless, the deposition of nano-layers requires precise control over both thickness and morphology. In this work, we investigate the optical properties and morphological characteristics of Liq thin films deposited via Organic Vapor Phase Deposition (OVPD). Specifically, we present our methodology for analyzing the measured pseudodielectric function <ε(ω)> using Spectroscopic Ellipsometry (SE), alongside the nano-topography of evaporated Liq nano-layers using Atomic Force Microscopy (AFM). This information can contribute to the understanding of the functionality of this material, since ultra-thin Liq interlayers can significantly increase the operational stability of OLED architectures.

Simultaneous control of carrier transport and film polarization of emission layers aimed at high-performance OLEDs

The orientation of a permanent dipole moment during vacuum deposition results in the occurrence of spontaneous orientation polarization (SOP). Previous studies reported that the presence of SOP in organic light-emitting diodes (OLEDs) lowers electroluminescence efficiency because electrically generated excitons are seriously quenched by SOP-induced accumulated charges. Thus, the SOP in a host:guest-based emission layer (EML) should be finely controlled. In this study, we demonstrate the positive effect of dipole-dipole interactions between polar host and polar emitter molecules on the OLED performance. We found that a small-sized polar host molecule that possesses both high molecular diffusivities and moderate permanent dipole moment, well cancels out the polarization formed by the SOP of the emitter molecules in the EML without a disturbance of the emitter molecules’ intrinsic orientation, leading to high-performance of OLEDs. Our molecular design strategy will allow emitter molecules to pull out the full potential of the EMLs in OLEDs.

Enhancement of Blue Doping-Free and Hyperfluorescent Organic Light Emitting Diode Performance through Triplet–Triplet Annihilation in the Derivatives of Anthracene and Carbazole

Enhancement of Blue Doping-Free and Hyperfluorescent Organic Light Emitting Diode Performance through Triplet–Triplet Annihilation in the Derivatives of Anthracene and Carbazole

Boosting Hole Mobility: Indenofluorene-Arylamine Copolymers and Their Impact on Solution-Processed OLED Performance.

We introduce three newly designed thermally cross-linkable hole transport copolymers (PIF-TPD, PIF-F2PCz, and PIF-TPAPCz) for improving the performance of solution-processed organic light-emitting diodes (s-OLEDs). These copolymers, designed through a strategic molecular approach with benzocyclobutene (BCB) and styrene-based cross-linking monomers, show high solvent resistance at a low cross-linking temperature (150 °C). Furthermore, these conjugated copolymers based on planar indenofluorene with three different hole transport (HT) units, exhibit outstanding charge carrier mobility (1.61 × 10-2 cm2 V-1s-1), demonstrated by comparing hole reorganization energy and electronic coupling strength of HT units. Despite these copolymers showing the overall vertical orientation in the horizontal dipole moment measurement results, we demonstrated that the HT units can exhibit the preferred orientation, contributing to high hole transport properties. As a result, they perform exceptionally well as hole transport layers in green phosphorescent s-OLEDs, achieving a maximum external quantum efficiency of 15.3% and a maximum current efficiency of 53.9 cd A-1 with a small efficiency roll-off despite their relatively low triplet energy levels. These results are comparable to vacuum-deposited OLEDs, highlighting the potential of these copolymers in advancing OLED technology for display panels and lighting applications.

Rational Design of Coumarin-Based Hybridized Local and Charge-Transfer Blue Emitters for Solution-Processed Organic Light-Emitting Diodes.

Hybridized local and charge-transfer (HLCT) with the utilization of both singlet and triplet excitons through the "hot excitons" channel have great application potential in highly efficient blue organic light-emitting diodes (OLEDs). The proportion of charge-transfer (CT) and locally excited (LE) components in the relevant singlet and triplet states makes a big difference for the high-lying reverse intersystem crossing process. Herein, three novel donor (D)-acceptor (A) type HLCT materials, 7-([1,1'-biphenyl]-4-yl(9,9-dimethyl-9H-fluoren-2-yl)amino)-3-phenyl-1H-isochromen-1-one (pPh-7P), 7-([1,1'-biphenyl]-4-yl(9,9-dimethyl-9H-fluoren-2-yl)amino)-3-methyl-1H-isochromen-1-one (pPh-7M), and 6-([1,1'-biphenyl]-4-yl(9,9-dimethyl-9H-fluoren-2-yl)amino)-3-methyl-1H-isochromen-1-one (pPh-6M), were rationally designed and synthesized with diphenylamine derivative as donor and oxygen heterocyclic coumarin moiety as acceptors. The proportions of CT and LE components were fine controlled by changing the connection site of diphenylamine derivative at C6/C7-position and the substituent at C3-position of coumarin moiety. The HLCT characteristics of pPh-7P, pPh-7M, and pPh-6M were systematically demonstrated through photophysical properties and density functional theory calculations. The solution-processed doped OLEDs based on pPh-6M exhibited deep-blue electroluminescence with the maximum emission wavelength of 446 nm, maximum luminance of 8755 cd m-2, maximum current efficiency of 5.83 cd A-1, and maximum external quantum efficiency of 6.54 %. The results reveal that pPh-6M with dominant 1LE and 3CT components has better OLED performance.

Achieving Deep‐Blue Through‐Space Charge‐Transfer Emitter by Designing the Donor‐π‐Donor‐σ‐Acceptor Molecular Structure

AbstractIn the realm of organic light‐emitting diode (OLED), through‐space charge transfer (TSCT) thermally activated delayed fluorescence (TADF) emitters have demonstrated remarkable achievements. Nevertheless, realizing both deep‐blue emission and high efficiency by the TSCT strategy remains a persistent challenge. Here, the novel donor‐π‐donor‐σ‐acceptor (D‐π‐D‐σ‐A) type deep‐blue TSCT emitter, namely D‐tCz‐BO, is formulated to investigate its performance in OLED. D‐tCz‐BO show a narrow deep‐blue emission and efficient TADF character (λPL = 448, FWHM = 54 nm, ΦPL = 82%, and ΔEST = 0.09 eV). More importantly, the OLED based on D‐tCz‐BO as the emitter showed a maximum external quantum efficiency (EQEmax) of 20.5%, with a Commission Internationale de l'Eclairage (CIE) coordinate of (0.14, 0.12). This represents one of the best deep‐blue TSCT‐TADF emitters to date.

Effective donor and acceptor modifications of carbazole-benzonitrile thermally activated delayed fluorescence molecules enabling high-performance OLEDs

Carbazole-benzonitrile derivatives (CzBNs) have great potential to enable thermally activated delayed fluorescence (TADF) molecules with both high efficiency and good stability simultaneously. However, the device performances of most CzBN-based organic light-emitting diodes (OLEDs) still lag behind other types of TADF molecules. In this work, we proposed a design strategy to construct efficient CzBN-TADF molecules through acceptor and donor modifications. The cyano-modified acceptor enables the extension of the lowest unoccupied molecular orbital while mostly preserving the overlapped area with the highest occupied molecular orbital. The optimized distributions of frontier molecular orbitals contribute to tiny singlet-triplet energy gaps while maintaining a high radiative decay rate. The incorporation of tert-butyl units in the donor groups further enhances the TADF property of resulted tPCNBN molecule due to suppressed non-radiative decay and reduced exciton self-quenching. Accordingly, OLEDs based on tPCNBN present the best device performances, such as a maximum external quantum efficiency of 33.1 % at 400 cd m−2, which is still as high as 26.3 % at a high luminance of 4000 cd m−2, demonstrating relatively low efficiency roll-off. These results confirm the effectiveness of the proposed design strategy in developing efficient and stable CzBN-TADF materials and devices.

Understanding of complex spin up-conversion processes in charge-transfer-type organic molecules

Despite significant progress made over the past decade in thermally activated delayed fluorescence (TADF) molecules as a material paradigm for enhancing the performance of organic light-emitting diodes, the underlying spin-flip mechanism in these charge-transfer (CT)-type molecular systems remains an enigma, even since its initial report in 2012. While the initial and final electronic states involved in spin-flip between the lowest singlet and lowest triplet excited states are well understood, the exact dynamic processes and the role of intermediate high-lying triplet (T) states are still not fully comprehended. In this context, we propose a comprehensive model to describe the spin-flip processes applicable for a typical CT-type molecule, revealing the origin of the high-lying T state in a partial molecular framework in CT-type molecules. This work provides experimental and theoretical insights into the understanding of intersystem crossing for CT-type molecules, facilitating more precise control over spin-flip rates and thus advancing toward developing the next-generation platform for purely organic luminescent candidates.

Solution-processed orange organic light-emitting diodes based on phosphorescent iridium(III) complexes with coumarin 6 as the main ligand

Four ionic orange phosphorescent iridium(III) complexes (Ir1, Ir2, Ir3, Ir4) were successfully synthesized using coumarin 6 as the cyclometalated ligand and 2,2′-bipyridine (bpy) derivatives with different number and position of methyl groups as the auxiliary ligand. The effects of substituents in the auxiliary ligands on their properties were systematically investigated. These four complexes exhibited orange emission at wavelengths of 590, 588, 587, and 586 nm, respectively, with excellent solubility and remarkable photophysical properties in different solvents. Furthermore, they were further applied in the organic light-emitting diodes (OLEDs) based on solution method. The maximum luminance of the devices based on Ir1/Ir2/Ir3/Ir4 reached 1907.0/932.6/760.8/519.3 cd/m2, with corresponding maximum current efficiency (CE), power efficiency (PE), and external quantum efficiency (EQE) values of 1.56/1.71/1.97/1.52 cd/A, 0.33/0.32/0.35/0.27 lm/W, and 0.77/0.82/0.90/0.72 %, respectively. Although there is room for improvement in the performance of OLEDs, this strategy inspires us to modulate the novel photoluminescent and electroluminescent properties of iridium(III) complexes through rational modifications of their ancillary ligands.

Effect of the Glass Transition Temperature of Organic Materials on Exciton Recombination Region of Deep Blue OLED under Thermal Stress

The carrier transport and the exciton recombination region, which are strongly affected by temperature, are essential to organic light‐emitting diodes (OLEDs) under thermal stress. A different charge carrier transport materials with different glass transition temperature (Tg) is selected to investigate their effect on the thermal stability of OLEDs. By calculating the carrier mobility at different annealing temperatures and comparing the simulated values by the Arrhenius equation, the effect of the thermal stress on the performance of OLEDs is analyzed. Then, using the luminescent dye as a probe adjacent to the emitting layer and charge transporting layer to identify the exciton recombination region at different temperatures and driving voltages, it is revealed that replacing the functional material with low Tg with a high Tg one could effectively increase the thermal stability of the device to 100 °C. The optimized devices have a reduced turn‐on voltage, and the electron mobility is increased by more than one order of magnitude, which was conducive to exciton recombination. The work promotes the application of OLEDs in extreme environments by improving their thermal stability.

Improving electron transportation and operational lifetime of full color organic light emitting diodes through a "weak hydrogen bonding cage" structure.

Efficient electron-transporting materials (ETMs) are critical to achieving excellent performance of organic light-emitting diodes (OLEDs), yet developing such materials remains a major long-term challenge, particularly ETMs with high electron mobilities (μeles). Herein, we report a short conjugated ETM molecule (PICN) with a dipolar phenanthroimidazole group, which exhibits an electron mobility of up to 1.52 × 10-4 cm2 (V-1 s-1). The origin of this high μele is long-ranged, regulated special cage-like interactions with C-H⋯N radii, which are also favorable for the excellent efficiency stability and operational stability in OLEDs. It is worth noting that the green phosphorescent OLED operation half-lifetimes can reach up to 630 h under unencapsulation, which is 20 times longer than that based on the commonly used commercial ETM TPBi.

Unveiling the photophysical and excited state properties of multi-resonant OLED emitters using combined DFT and CCSD method.

Multi-resonance thermally-activated delayed fluorescence (MR-TADF) is predominantly observed in organoboron heteroatom-embedded molecules, featuring enhanced performance in organic light-emitting diodes (OLEDs) with high color purity, chemical stability, and excellent photoluminescence quantum yields. However, predicting the impact of any chemical change remains a challenge. Computational methods including density functional theory (DFT) still require accurate descriptions of photophysical properties of MR-TADF emitters. To circumvent this drawback, we explored recent investigations on the CzBX (Cz = carbazole, X = O, S, or Se) molecule as a central building block. We constructed a series of MR-TADF molecules by controlling chalcogen atom embedding, employing a combined approach of DFT and coupled-cluster (CCSD) methods. Our predicted results for MR-TADF emitter molecules align with the reported experimental data in the literature. The variation in the positions of chalcogen atoms embedded within the CzBX2X framework imparts unique photophysical properties.

Recent progress in multi-resonance thermally activated delayed fluorescence emitters with an efficient reverse intersystem crossing process.

Multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters have become an active research topic at the forefront of organic light-emitting diodes (OLEDs) owing to their excellent photophysical properties such as high efficiency and narrow emission characteristics. However, MR-TADF materials always exhibit slow reverse intersystem crossing rates (kRISC) due to the large energy gap and small spin-orbit coupling values between singlet and triplet excited states. In order to optimize the RISC process, strategies such as heavy-atom-integration, metal perturbation, π-conjugation extension and peripheral decoration of donor/acceptor units have been proposed to construct efficient MR-TADF materials for high-performance OLEDs. This article provides an overview of the recent progress in MR-TADF emitters with an efficient RISC process, focusing on the structure-activity relationship between the molecular structure, optoelectronic feature, and OLED performance. Finally, the potential challenges and future prospects of MR-TADF materials are discussed to gain a more comprehensive understanding of the opportunities for efficient narrowband OLEDs.

High-performance solution-deposited ambipolar Ir(III) complex phosphors with aggregation-induced phosphorescence enhancement behavior based on N-P=O resonant variation skeleton

Ir(III) complex phosphors with both ambipolar feature and aggregation-induced phosphorescence enhancement (AIPE) property are promising to furnish high electroluminescent performance for solution-deposited phosphorescent organic light-emitting diodes. However, the molecular design...