Electroluminescence Performance Research Articles

Fabrication of high performance based deep-blue OLED with benzodioxin-6-amine-styryl-triphenylamine and carbazole hosts as electroluminescent materials

The present study reports synthesis of phenathroimidazole derivatives structures following donor–acceptor relation for high performance deep-blue light emitting diodes. Herein, methyl substituted benzodioxin-6-amine phenanthroimidazoles Cz-SBDPI and TPA-SBDPI derivatives that provide the blue light were designed and synthesized. These Cz-SBDPI and TPA-SBDPI show higher glass transition (Tg) temperatures of 199 and 194 °C and demonstrate enhanced thermal properties. Apart from enhanced thermal stability these compounds also exhibit superior photophysical, electrochemical and electroluminescent properties. The non-doped carbazole based device display improved electroluminescent performances than those of TPA-based devices. The strong orbital-coupling due to decreased energy barrier between Cz-SBDPI transitions result in deep blue emission with CIE—0.15, 0.06. For non-doped Cz-SBDPI device; high L (brightness):12,984 cd/m2; ηc (current efficiency): 5.9 cd/A; ηp (power efficiency): 5.7 lm/W and ηex (external quantum efficiency): 6.2% was observed. The results show that the D–A emitters can serve as simple but also as an effective approach to devise cheap electroluminescent materials that has high efficiency and can serve as OLED devices.

Thermally-stable and color-tunable novel single phase phosphor Ca2GaTaO6:Dy3+, Sm3+ for indoor lighting applications

This study successfully synthesized novel phosphors Ca2GaTaO6:xDy3+ (CGTO:xDy3+) and Ca2GaTaO6:0.06Dy3+, ySm3+ (CGTO:0.06Dy3+, ySm3+) using the high temperature solid-phase reaction preparation. The microstructure, optical properties, and energy transfer mechanism of the phosphors were studied through X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL) spectra and fluorescence lifetimes. XRD and corresponding refinement results indicate that Dy3+ and Sm3+ ions were effectively doped into the Ca2GaTaO6 (CGTO) lattice. The SEM graphs show that the elements in CGTO:0.06Dy3+, 0.5Sm3+ phosphors are uniformly distributed. PL spectra analysis show the CGTO:xDy3+ phosphors display two strong emission peaks located at 482 nm for blue emission and 575 nm for yellow emission when excited with 350 nm light. Under uniform conditions, when excited with 365 nm of light, the CGTO:0.06Dy3+, ySm3+ phosphors emit light that can be tuned with adjustable color coordinates and correlated color temperature (CCT) by incorporating varying proportions of Sm3+ ions. This tunability is achieved through the effective energy migration from Dy3+ to Sm3+ ions within the phosphor material. Furthermore, the emission spectra and weaken lifetimes of the CGTO:0.06Dy3+, ySm3+ confirm the energy transport between Dy3+ and Sm3+, and the energy transfer efficiency reached to 76 %. At 423 K, the luminescence intensity of CGTO:0.06Dy3+, 0.05Sm3+ phosphor retains 87 % of the intensity observed at 298 K, signifying its excellent thermal durability. Finally, the electroluminescent performance of the CGTO:0.06Dy3+ and CGTO:0.06Dy3+, 0.05Sm3+ phosphors packaged on 365 nm light-emitting diode (LED) chips respectively were studied to investigate the capability applications of the phosphors in white light-emitting diodes (WLEDs) field. The CCT of the packaged LEDs decline from 3396 to 2825 K, indicating CGTO:0.06Dy3+, 0.05Sm3+ phosphor shifts to warmer white light. At a voltage input of 3.4 V and a current of 600 mA, the thermal sensing shows that the WLEDs maintain aptitude for 90 min, showing that the packaged WLEDs can function consistently under elevated temperatures. These studies indicated the phosphors have potential applications in indoor lighting.

Light Out‐Coupling for High‐Performance Quantum Dot Light‐Emitting Diodes by π‐π Oriented PEDOT: PSS

AbstractBreaking the theoretical limits of external quantum efficiency (EQE) and obtaining quantum dot light‐emitting diodes (QLEDs) with high brightness, high efficiency, and low operating voltage is the basis of commercial applications in display and illumination. Devices with an EQE of over 20% can be realized by carrier equilibrium injection and light out‐coupling enhancement. However, it is difficult to synergistically enhance the performance of QLEDs by combining the light out‐coupling and the hole enhancement injection. In this paper, the injection enhancement of holes and the light out‐coupling are realized simultaneously only by nano‐imprint lithography (NIL). The π─π bonds of the PEDOT: PSS film treated by NIL demonstrate a molecular orientation perpendicular to the substrate, which improves the injection of the hole. The PEDOT: PSS patterned by NIL further presents improved light out‐coupling. Consequently, the EQE of red‐QLED is 30.42% with a synergistic enhancement factor of 61%, accompanying the maximum brightness increased by 8% to 125 200 cd m−2 at 4.6 V (Vturn‐on, 1.74 V). The EQE and brightness of green‐QLED increased by 38.9% and 34.3% to 24.16% and 279 700 cd m−2, respectively. Therefore, NIL will provide new insights into synergistically enhancing light out‐coupling and internal quantum efficiency to break through the performance of electroluminescence (EL).

Differences in Electron and Hole Injection and Auger Recombination between Red, Green, and Blue CdSe-Based Quantum Dot Light Emitting Devices.

Despite the significant progress that has been made in recent years in improving the performance of quantum dot light-emitting devices (QLEDs), the effect of charge imbalance and excess carriers on excitons in red (R) vs green (G) vs blue (B) QLEDs has not been compared or systematically studied. In this work we study the effect of changing the electron (e)/hole (h) supply ratio in the QDs emissive layer (EML) in CdSe-based R-, G-, and B-QLEDs with inverted structure in order to identify the type of excess carriers and investigate their effect on the electroluminescence performance of QLEDs of each color. Results show that in R-QLEDs, the e/h ratio in the EML is >1, whereas in G- and B-QLEDs, the e/h ratio is <1 with charge balance conditions being significantly worse in the case of B-QLEDs. Transient photoluminescence (PL) and steady state PL measurements show that, compared to electrons, holes lead to a stronger Auger quenching effect. Transient electroluminescence (TrEL) results indicate that Auger quenching leads to a gradual decline in the EL performance of the QLEDs after a few microseconds, with a stronger effect observed for positive charging versus negative charging. The results provide insights into the differences in the efficiency behavior of R-, G-, and B-QLEDs and uncover the role of excess holes and poor charge balance in the lower efficiency and EL stability of B-QLEDs.

Acceptor–donor–acceptor based thermally activated delayed fluorescent materials: structure–property insights and electroluminescence performances

Thermally activated delayed fluorescent (TADF) materials shown great attention in Organic light-emitting diodes (OLEDs). Herein, we have systematically reviewed the Acceptor–Donor–Acceptor based TADF materials with electroluminescent characteristics.

Structure modification and luminescence regulation in new violet light excitable Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ phosphors via cation substitution.

Cyan-emitting phosphors are urgently needed to address the "cyan gap" in artificial full-spectrum lighting. In this research, a series of Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ (0.005 ≤ x ≤ 0.08, 0.0 ≤ y ≤ 2.0) phosphors with tunable luminescence was synthesized. Through cation regulation, the luminescence color of Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ can be adjusted from yellow to cyan. Crystal structure analysis revealed that Eu2+ ions simultaneously occupy [Sr1/Ba1Y1La1] and [Sr2/Ba2Y2La2] sites, resulting in multiple luminescence centers and a broadened emission spectrum. With increasing Ba2+ ion concentration, the PLE spectrum was red-shifted from 337 nm to 372 nm, and the excitation intensity in the violet region was significantly enhanced, making it more compatible with violet LED chips. Meanwhile, the PL spectrum was blue-shifted from 543 nm to 496 nm with increasing Ba2+ concentration, accompanied by an increase of about 10 times in the excitation and emission intensity. The optimized Ba2Y4La4(SiO4)6O2:0.02Eu2+ phosphor can be excited by violet light and emits bright cyan light effectively, which can be used to fill the "cyan gap". Eventually, a series of white LED devices was manufactured by combining the as-prepared luminescence-tunable phosphors with commercial phosphors. Among them, the 410 nm violet LED chip-based WLED(Ba2) device comprising Ba2Y4La4(SiO4)6O2:0.02Eu2+ exhibited the best electroluminescence performance, increasing the color rendering index from 82.0 to 98.6, verifying the compensation effect of the Ba2Y4La4(SiO4)6O2:Eu2+ phosphor on cyan light.

Thermally activated delayed fluorescence tetradentate ligand-containing gold(III) complexes with preferential molecular orientation and their application in organic light-emitting devices.

A new class of thermally activated delayed fluorescence (TADF) pyridine-/pyrazine-containing tetradentate C^C^N^N gold(III) complexes have been designed and synthesized. Displaying photoluminescence quantum yields (PLQYs) of up to 0.77 in solid-state thin films, these complexes showed at-least a six-fold increase in the radiative decay rate constant (kr) in toluene upon increasing temperature from 210 to 360 K. Using variable-temperature (VT) ultrafast transient absorption (TA) spectroscopy, the reverse intersystem crossing (RISC) processes were directly observed and the activation parameters were determined, in line with the results of the Boltzmann two-level model fittings, in which the energy separation values between the lowest-lying singlet excited state (S1) and the lowest-lying triplet excited state (T1), ΔE(S1-T1), of these complexes were estimated to be in the range of 0.16-0.18 eV. Through strategic modification of the position of the electron-donating -tBu substituent in the cyclometalating ligand, the permanent dipole moments (PDMs) of these tetradentate gold(III) emitters could be manipulated to enhance their horizontal alignment in the emitting layer of organic light-emitting devices (OLEDs). Consequently, the resulting vacuum-deposited OLEDs demonstrated a 30% increase in the theoretical out-coupling efficiency (ηout), as well as promising electroluminescence (EL) performance with maximum external quantum efficiencies (EQEs) of up to 15.7%.

Plasmonically-boosted exciton-photon coupling strength in a near-infrared LED based on a ZnO:Ga microwire/GaAs heterojunction with surface-coated Au&Ag alloy nanorods.

The development of electrically-driven low-dimensional coherent light sources via highly-polarized polariton emission behavior has been extensively researched, but suffers from limited modulation of the exciton-photon coupling strengths. Herein, an electrically-biased near-infrared exciton-polariton light-emitting diode (LED), which includes a Ga-doped ZnO microwire (ZnO:Ga MW) and p-type GaAs substrate, is demonstrated. The well-designed LED structure is conducive to producing strong coupling between excitons and cavity photons, thus yielding highly-polarized light-emissions due to the optical birefringence in the ZnO:Ga MW microcavity. In particular, when the LED device is modified using Au&Ag alloy nanorods (AuAgNRs) with desired plasmonic properties, the electroluminescence (EL) performance is significantly boosted, especially the Rabi-splitting energy, which increases from 96 to 285 meV. The current-injection exciton-polariton emission from the LED undergoing a strong coupling regime is confirmed through angle-resolved EL measurements. This study exhibits a performance-boosted near-infrared exciton-polariton LED at room temperature, which provides a new scheme toward the realization of highly energy-efficient polariton coherent light sources. Further, the significantly lower density of polariton states induced by the incorporated metal nanostructures highlights a bright future of realizing ultralow-threshold polariton lasers much more feasibly, in comparison to conventional lasers based on narrow bandgap semiconductors.

Post-hot-cast annealing deposition of perovskite films with infused multifunctional organic molecules to enhance the performance of large-area light-emitting devices.

All-inorganic perovskites show great promise as an emission layer in perovskite light-emitting diodes (PeLEDs) owing to their easy solution processing, low manufacturing cost, and excellent optoelectronic properties. However, there is still an immense performance gap from small-area devices to large-area PeLED devices. The inhomogeneity of large-area high-quality perovskite films inevitably leads to vast defects and electroluminescence performance losses. Herein, a post-hot-cast annealing deposition scheme and the introduction of the multifunctional molecule 2-amino-1,3-propanediol (APDO) were proposed to regulate the crystallization of the perovskite film. As a result, uniform APDO:CsPbBr2.5Cl0.5 perovskite films with high crystallinity and lower defect density were deposited by post-hot-cast annealing. A decent maximum brightness of 2659 cd m-2 was achieved for the large-area cyan PeLEDs with an emitting area of 400 mm2.

A multi-resonance emitter with five-membered thiophene as the π-core enables efficient, narrowband and reduced efficiency roll-off OLEDs.

Efficient, narrowband multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters have recently sparked significant interest in high-resolution organic light-emitting diode (OLED) displays. However, almost all the progress in MR-TADF materials has been accomplished using a six-membered ring as the π-core to date. Herein, we present the first example of a five-membered ring π-core-based MR-TADF emitter named Th-BN developed by introducing thiophene instead of hexagonal benzene as the π-core. The introduction of thiophene significantly enhances intramolecular charge transfer intensity and the spin-orbit coupling matrix elements but does not change the intrinsic MR properties. As a result, Th-BN exhibits a narrowband green emission at 512 nm, with a high luminous efficiency of 97%, a narrow full-width at half maximum of 41 nm/0.20 eV, and a rapid reverse intersystem crossing rate of 18.7 × 104 s-1, which is 10 times higher than that of its benzenoid counterpart DtBuCzB. The corresponding green OLEDs based on Th-BN achieve excellent electroluminescence performance with an external quantum efficiency (EQE) of 34.6% and a reduced efficiency roll-off with an EQE of 26.8% at a high luminance of 1000 cd m-2.

An unprecedented {Y2⊂Y10} type disk-like Y12 nanocluster featuring electroluminescence property in OLED device

An unprecedented disk-like Y12 cluster with unique Y2⊂Y10 type structure was achieved successfully, which is the largest non-brucite type disk-like RE cluster and exhibits obvious electroluminescence performance in OLED device.

Enhanced chiroptical activity for narrow deep-blue emission in axial chiral frameworks via three-dimensional interlocking.

The advancement of desirable circularly polarized luminescence (CPL) emitters is predominantly constrained by the effective regulation of magnetic and electric transition vectors, particularly within the deep-blue spectral domain. Herein, we present four pairs of novel chiral emitters with systematically varied molecular rigidity, symmetry, and chiral centers to elucidate the intrinsic coupling of key molecular parameters influencing their chiroptical properties. Notably, the incorporation of appropriate intramolecular 3D-interlocking within a natural binaphthyl chirality skeleton offers an effective approach to achieving both significantly narrowed full width at half maximum (FWHM, as low as 18 nm) and substantially enhanced chiroptical activity (luminous dissymmetry factor, g PL, up to 3.0 × 10-3). Additionally, introducing a secondary chiral center closely parallel to the primary chiral plane facilitates strong chiral-chiral interactions, further affording a 50% improvement in their g PL values. As a demonstration, vacuum-deposited circularly polarized organic light-emitting diodes incorporating these pure fluorescent emitters exhibit outstanding electroluminescent performance, with maximum external quantum efficiency exceeding 5.35%, favorable FWHM of approximately 25 nm, and extreme CIE y values below 0.03.

Highly efficient circularly polarized electroluminescence based on chiral manganese(ii) complexes.

Currently reported circularly polarized luminescent devices are primarily based on rare earth and noble metal complexes or lead perovskite materials. Reports on electroluminescent devices employing eco-friendly luminescent materials are notably scarce. In this study, we strategically designed and synthesized manganese complexes featuring Binapo as the chiral ligand. The complex structure reveals a tetrahedral coordination configuration, with the R/S configurations exhibiting a mirror relationship. Leveraging the strong ligand field and chiral structural characteristics of Binapo, the enantiomers display red emission and exhibit significant circularly polarized luminescence with a circularly polarized luminescence asymmetric factor (g lum) of 5.1 × 10-3. The circularly polarized electroluminescent performance was investigated by using a solution processing method and host-guest doping strategy. Our efforts resulted in device performance with an external quantum efficiency (EQE) exceeding 4%, and its electroluminescent asymmetric factor (g EL) reached an impressive -8.5 × 10-3. This surpasses the performance of most devices relying on platinum (Pt) and iridium (Ir) metal complexes and perovskite related materials. Our work establishes a pathway for the development of cost-effective and environmentally friendly chiral electroluminescent materials and devices.

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...

Luminescent carbene-copper(i)-amide polymers for efficient host-free solution-processed OLEDs.

Luminescent metallopolymers have attracted broad interest in the fields of healthcare and organic electronics. However, polymeric emitters based on earth-abundant metal complexes are scarce. Here, two series of Cu(i) polymers, PMAC-x and PCAAC-x (x = 1-3) have been developed using two kinds of Cu(i)-based carbene-metal-amide (CMA) complexes as side-chain emitter units to combine with a nonconjugated polystyrene backbone. These Cu(i) polymers emit via distinct thermally activated delayed fluorescence or dominant phosphorescence, inherited from the grafted Cu(i)-based CMA units. Particularly, the PMAC-x polymers exhibit high photoluminescence quantum efficiencies of up to 0.78, short emission lifetimes of down to 0.66 μs, and fast radiative rates of up to 106 s-1 in neat films. Thanks to the good encapsulation effect of the polystyrene backbone, these Cu(i) polymers not only demonstrate favorable moisture stability but also show significant aggregation-induced emission. The resultant host-free solution-processed organic light-emitting diodes (OLEDs) achieve outstanding electroluminescence performance with a record external quantum efficiency of 13.8% at a practical luminance of ∼100 nits, representing state-of-the-art device efficiency for metallopolymer-based OLEDs. This work not only presents the first example of CMA polymers but also provides the future direction of polymeric emitters from earth-abundant metal complexes for the OLED application.

Supersensitive detection of lincomycin with an ECL aptasensor based on the synergistic integration of gold-functionalized upconversion nanoparticles and thiolated 3,4,9,10-perylene tetracarboxylic acid.

In this work, the supersensitive and selective determination of lincomycin (Lin) was achieved using a novel electroluminescent (ECL) aptasensor based on the synergistic integration of gold functionalized upconversion nanoparticles (UCNPs) and thiolated 3,4,9,10-perylene tetracarboxylic acid (PTCA). The integration of two luminophores of UCNPs and PTCA combined the merits of the cathodoluminescence stability of UCNPs and the high quantum yield of PTCA, which significantly promoted the ECL signal and analytical performance of the proposed sensor. The introduction of gold nanoparticles in UCNPs can not only improve the conductivity and ECL performance of UCNPs but also cause them to easily integrate with thiolated PTCA (t-PTCA) via an Au-S bond. The ECL signal of UCNPs@Au/t-PTCA/GCE was almost twice as strong as that of t-PTCA/GCE and tenfold higher than that of UCNPs@Au/GCE. Because of the non-conductive protein of the Lin aptamer, the ECL intensity of apt/UCNPs@Au/t-PTCA/GCE noticeably decreased. In the presence of Lin, the aptamer was pulled down from the sensing interface, resulting in the recovery of the ECL intensity of the sensor. Under optimal conditions, our proposed sensor can quantify the concentration of Lin in the range from 1.0 × 10-15 to 1.0 × 10-7 M with a low detection limit of 2.4 × 10-16 M (S/N = 3), exhibiting high sensitivity and specificity for the determination of Lin.

Aromatic ammonium salts ligand engineering-assisted CsPbBr3 quantum dots enable electroluminescent solar cell

All-inorganic perovskite quantum dots (QDs) have gained significant attention for their excellent optoelectronic properties, making them promising materials for applications in light-emitting diodes (LEDs) and solar cells (SCs), but it is still a challenge to balance colloidal stability of QDs and conductivity of QD films. To address the issue, an effective surface ligand engineering method has been employed by using phenethylammonium bromide (PEABr) to passivate the surface defects of QDs while enhancing the charge transport and injection in QD films. The results indicate that PEABr ligand has successfully been adsorbed onto the surface of CsPbBr3 QDs to passivate the vacancy defects, significantly enhance the electronic coupling between QDs. Systematically experimental studies show that PEABr post-treatment improves the PLQY (85 %) and stability of QDs with enhanced the carrier transport in QD film. Thanks to enhanced optoelectronic performance, the fabricated devices exhibited excellent photovoltaic (PV) and electroluminescent (EL) performance, and the CsPbBr3 QD SC had a PCE of 2.00 % while exhibiting a maximum luminance (Lmax) of 1512 cd cm−2, thus realizing high-performance electroluminescent solar cell.

Fully space-confined donor-acceptor interaction for highly efficient thermally activated delayed fluorescence emitters

The emerging through-space charge transfers (TSCT) emitters with thermally activated delayed fluorescence (TADF) have drawn increasing interest. However, the low luminescence efficiency and slow reverse intersystem crossing (RISC) always limit their device performances. A new molecular design strategy for TSCT-TADF emitters with a fully space-confined donor/acceptor conformation that integrates high luminescence efficiency and fast RISC is proposed herein. Two new TSCT-TADF emitters, TRZ-STFMe and TRZ-STFPh, are developed by introducing the methyl and phenyl substituents at the C2 of the rigid fluorene scaffold, respectively. The repulsive interaction between methyl and the acceptor induces a close and face-to-face donor–acceptor stacking to generate highly efficient TADF and suppress structural changes during the RISC process in TRZ-STFMe. In contrast, TRZ-STFPh shows relatively low luminescence efficiency and slow RISC because of its conformationally unstable phenyl substituent. With a high luminescence efficiency of 97 % and a significant RISC rate of 5.23 × 105 s−1, TRZ-STFMe demonstrates a high electroluminescence performance with a maximum external quantum efficiency (EQE) of 29.6 % and an EQE of 26.5 % at 1000 cd m−2.

Molecular Engineering Modulating the Singlet-Triplet Energy Splitting of Indolocarbazole-Based TADF Emitters Exhibiting AIE Properties for Nondoped Blue OLEDs with EQE of Nearly 20.

The development of efficient blue thermally activated delayed fluorescence (TADF) emitters with an aggregation-induced emission (AIE) nature, for the construction of organic light-emitting diodes (OLEDs), is still insufficient. This can be attributed to the challenges encountered in molecular design, including the inherent trade-off between radiative decay and reverse intersystem crossing (RISC), as well as small singlet-triplet energy splitting (ΔEST) and the requirement for high photoluminescence quantum yields (ΦPL). Herein, we present the design of three highly efficient blue TADF molecules with AIE characteristics by combining π-extended donors with different acceptors to modulate the differences in the electron-donating and electron-withdrawing abilities. This approach not only ensures high emission efficiency by suppressing close π-π stacking, weakening nonradiative relaxation, and enhancing radiative transition but also maintains the equilibrium ratio between the triplet and singlet excitons by facilitating the process of RISC. These emitters exhibit AIE and TADF properties, featuring quick radiative rates and low nonradiative rates. The ΦPL of these emitters reached an impressive 88%. Based on their excellent comprehensive performance, nondoped PICzPMO and PICzPMO OLEDs achieved excellent electroluminescence performance, exhibiting maximum external quantum efficiency (EQEmax) of up to 19.5%, while the doped device achieved a higher EQEmax of 20.8%. This work demonstrated that by fusing π-extended large rigid donors with different acceptors, it is possible to regulate the difference in electron-donating and electron-withdrawing abilities, resulting in a small ΔEST, high ΦPL, and fast RISC process, which is a highly feasible strategy for designing efficient TADF molecules.

Conformational isomerization imparts low concentration dependence to multiple resonance thermally activated delayed fluorescence (MR-TADF) emitters

Electroluminescent performance of multiple resonance (MR) type thermally activated delayed fluorescence (TADF) emitters is highly dependent to the doping concentration due to the flat molecular structures, which is a major issue toward practical applications. Herein, an effective approach reducing the concentration dependence is proposed by introducing conformational isomerism for MR-TADF emitters. Two novel MR-TADF emitters were designed by decorating 10H-spiro[acridine-9,2′-adamantane] (a-DMAc) as a dual-conformational moiety onto the MR-core BNCz with different connection methods, which could induce different conformational distributions. In particular, the conformational isomerism of BNCz-aDMAC leads to a lower fraction of QE forms compared to the QE-dominant BNCz-PDMAC in amorphous doped film states with identical doping weights, thus enabling effective suppression of concentration quenching with barely harming color purity. Therefore, BNCz-aDMAC-based organic light-emitting diodes (OLEDs) demonstrate consistent and high efficiency over a wide doping range, maintaining a maximum external quantum efficiency of 23.8 % and a full width at half maximum of 31 nm even at a high doping ratio of 30 wt%.