Bright Light-emitting Diodes Research Articles

Blue Light-Emitting Diodes Based on Pure Bromide Perovskites.

Blue perovskite light-emitting diodes (LEDs) are essential for the creation of full-color displays and white-light illumination, and some significant progress is made in recent years. However, most high-performance blue perovskite LEDs are currently based on mixed-halide perovskites and suffer from unstable spectra due to inevitable halide phase segregation, which is unfavorable for the application of blue perovskite LEDs. In contrast, blue emissions from pure bromide perovskites generally exhibit stable spectra (consistent emission peak positions and spectral shapes) and are worthy of attention. In this review, the recent advances in blue LEDs based on pure bromide perovskites according to different strategies are classified and summarized. Moreover, the challenges related to poor charge injection, high defect-state density, lack of high-performance in the deeper blue region, and inferior operational stability are addressed. Finally, an outlook is provided on feasible future research directions for highly bright, efficient, and stable blue perovskite LEDs.

Hetero-Nucleation Induced [111]-Oriented Mixed Halide Perovskite for Stable Pure Red Light-Emitting Diodes.

Mixed halide 3D perovskites are promising for bright, efficient, and wide-color gamut light-emitting diodes (LEDs) due to their excellent carrier transport, high luminescence, and easily tunable bandgaps. However, serious halide ion migration inside mixed halide 3D perovskite results in poor operational and spectral stability of the as-fabricated LEDs. Here, a hetero-nucleation crystallization strategy is reported to grow [111]-orientationpreferred mixed halide 3D perovskite CsPbI3-xBrx thin films for stable pure red LEDs. This hetero-nucleation crystallization is enabled by the addition of phosphoric acid (H3PO4) complexation, which promotes the growth of small perovskite grains into large grains with uniform [111]-orientation. The obtained [111]-orientation preferred film exhibits excellent stability under light or electric field stimulus as revealed by model analysis and experimental results compared to that of [001]-orientation preferred film. Thus, based on the [111]-orientationpreferred film, the fabricated LED exhibits an external quantum efficiency of 22.8%, a maximum brightness of 12000cdm-2, and a half-life time of 4080min under 1.5mA cm-2. More importantly, the electroluminescence spectrum of the device remains stable during the continuous operation of 4080min, showcasing the significant spectral stability improvement enabled by the hetero-nucleation induced [111]-orientation strategy.

Toward Ultra-High Sensitivity Optical Thermometers and Bright Yellow LEDs Based on Phonon-Assisted Energy Transfer in Rare Earth-Doped La2ZnTiO6 Double Perovskite.

Double perovskites, a class of ceramic oxides with unique crystal structures and diverse physical properties, show promise for various technological applications including solar cells, photodetectors, and light-emitting diodes (LEDs). Despite limited research on rare earth-doped double perovskites, leveraging their ultrahigh luminous efficiency to achieve bright yellow LED emission and addressing energy transfer challenges between Yb3+ and Nd3+ ions in double perovskite La2ZnTiO6 with moderate phonon energy are explored in this work. Through phonon-assisted energy transfer, an ultrasensitive optical thermometer covering a wide temperature range is developed by utilizing the different temperature responses of Er3+ emission in the visible light region and Nd3+ emission in the near-infrared region based on the luminescence intensity ratio (LIR). All the results demonstrate that the rare earth (Yb-Er, Yb-Nd, and Yb-Nd-Er)-doped La2ZnTiO6 phosphors can be effectively utilized for ultrabright LED illumination and ultrahigh sensitivity self-calibrated temperature sensing. This research underscores the significance of phonon-assisted energy transfer in improving material properties and provides valuable insights for the advancement of multifunctional materials.

Hybrid Amino Acid Ligand-Regulated Excited Dynamics of Highly Luminescent Perovskite Quantum Dots for Bright White Light-Emitting Diodes.

Organic-inorganic hybrid perovskite quantum dots (QDs) have garnered significant research interest owing to their unique structure and optoelectronic properties. However, their poor optical performance in ambient air remains a significant limitation, hindering their advancement and practical applications. Herein, three amino acids (valine, threonine and cysteine) were chosen as surface ligands to successfully prepare highly luminescent CH3NH3PbBr3 (MAPbBr3) QDs. The morphology and XRD results suggest that the inclusion of the amino acid ligands enhances the octahedral structure of the QD solutions. Moreover, the observed blue-shifted phenomenon in the photoluminescence (PL) aligns closely with the blue-shifted phenomenon observed in the ultraviolet-visible (UV-Vis) absorption spectra, attributed to the quantum confinement effect. The time-resolved spectra indicated that the introduction of the amino acid ligands successfully suppressed non-radiative recombination, consequently extending the fluorescence lifetime of the MAPbBr3 QDs. The photoluminescence quantum yields (PLQYs) of the amino acid-treated MAPbBr3 QDs are increased by 94.8%. The color rendering index (CRI) of the produced white light-emitting diode (WLED) is 85.3, with a correlated color temperature (CCT) of 5453 K. Our study presents a novel approach to enhancing the performance of perovskite QDs by employing specially designed surface ligands for surface passivation.

Spectrally Stable and Bright Red Perovskite Light-Emitting Diodes.

Mixing iodide and bromide in three-dimensional metal-halide perovskites is a facile strategy for achieving red light-emitting diodes (LEDs). However, these devices often face challenges such as instability in electroluminescence spectra and low brightness due to phase segregation in mixed-halide perovskites. Here, we demonstrate spectrally stable and bright red perovskite LEDs by substituting some of the halide ions with pseudohalogen thiocyanate ions (SCN-). We find that SCN- can occupy halogen vacancies, thereby releasing microstrain and passivating defects in the perovskite crystals. This leads to the suppression of mixed-halide phase segregation under electrical bias. As a result, the red perovskite LEDs exhibit a high brightness of >35 000 cd m-2 with stable Commission Internationale de l'Eclairage (CIE) coordinates of (0.713, 0.282). This brightness surpasses that of the best-performing red perovskite LEDs, showing great promise for advancing perovskite LEDs in display and lighting applications.

Bright, Flexible, and Waterproof Top-Emitting InP Quantum Dot Light-Emitting Diodes on Al Foil

Bright, Flexible, and Waterproof Top-Emitting InP Quantum Dot Light-Emitting Diodes on Al Foil

Bright, efficient, and stable pure-green hyperfluorescent organic light-emitting diodes by judicious molecular design

To fulfill ultra-high-definition display, efficient and bright green organic light-emitting diodes with Commission Internationale de l’Éclairage y-coordinate ≥ 0.7 are required. Although there are some preceding reports of highly efficient devices based on pure-green multi-resonance emitters, the efficiency rolloff and device stabilities for those pure-green devices are still unsatisfactory. Herein, we report the rational design of two pure-green multi-resonance emitters for achieving highly stable and efficient pure-green devices with CIEx,ys that are close to the NTSC and BT. 2020 standards. In this study, our thermally activated delayed fluorescence OLEDs based on two pure-green multi-resonance emitters result in CIEy up to 0.74. In hyperfluorescent device architecture, the CIExs further meet the x-coordinate requirements, i.e., NTSC (0.21) and BT. 2020 (0.17), while keeping their CIEys ~ 0.7. Most importantly, hyperfluorescent devices display the high maximum external quantum efficiencies of over 25% and maximum luminance of over 105 cd m−2 with suppressed rolloffs (external quantum efficiency of ~20% at 104 cd m−2) and long device stabilities with LT95s of ~ 600 h.

Top-Down Exfoliation Process Constructing 2D/3D Heterojunction toward Ultrapure Blue Perovskite Light-Emitting Diodes.

3D perovskites with low energy disorder and high ambipolar charge mobility represent a promising solution for efficient and bright light-emitting diodes. However, the challenges of regulating the nanocrystal size to trigger the quantum confinement effect and control the surface trap states to reduce charge loss hinder the applications of 3D perovskites in blue perovskite light-emitting diodes (PeLEDs). In this study, we present a top-down exfoliation method to obtain blue 3D perovskite films with clipped nanocrystals and tunable bandgaps by employing methyl cyanide (MeCN) for post-treatment. In this method, the MeCN solvent exfoliates the surface components of the 3D perovskite grains through a partial dissolution process. Moreover, the dissolved precursor can be further utilized to construct an ingenious 2D/3D heterostructure by incorporating an organic spacer into the MeCN solvent, contributing to efficient defect passivation and improved energy transfer. Consequently, efficient PeLEDs featuring ultrapure blue emission at 478 nm achieve a record external quantum efficiency of 12.3% among their 3D counterparts. This work emphasizes the significance of inducing the quantum confinement effect in 3D perovskites for efficient blue PeLEDs and provides a viable scheme for the in situ regulation of perovskite crystals.

Bright and stable near-infrared lead-free perovskite light-emitting diodes

Long-wavelength near-infrared light-emitting diodes (NIR LEDs) with peak emission wavelengths beyond 900 nm are of critical importance for various applications including night vision, biomedical imaging, sensing and optical communications. However, the low radiance and poor operational stability of state-of-the-art long-wavelength NIR LEDs based on soft materials remain the most critical factors limiting their practical applications. Here we develop NIR LEDs emitting beyond 900 nm with improved performance through the rational manipulation of p doping in all-inorganic tin perovskites (CsSnI3) by retarding and controlling the crystallization process of perovskite precursors in tin-rich conditions. The resulting NIR LEDs exhibit a peak emission wavelength at 948 nm, high radiance of 226 W sr−1 m−2 and long operational half-lifetime of 39.5 h at a high constant current density of 100 mA cm−2. Our demonstration of efficient and stable NIR LEDs operating at high current densities may also open up new opportunities towards electrically pumped lasers.

Bright and Stable Yellow Quantum Dot Light-Emitting Diodes Through Core-Shell Nanostructure Engineering.

Solution-processed and efficient yellow quantum dot light-emitting diodes (QLEDs) are considered key optoelectronic devices for lighting, display, and signal indication. However, limited synthesis routes for yellow quantum dots (QDs), combined with inferior stress-relaxation of the core-shell interface, pose challenges to their commercialization. Herein, a nanostructure tailoring strategy for high-quality yellow CdZnSe/ZnSe/ZnS core/shell QDs using a "stepwise high-temperature nucleation-shell growth" method is introduced. The synthesized CdZnSe-based QDs effectively smoothed the release stress of the core-shell interface and revealed a near-unit photoluminescence quantum yield, with nonblinking behavior and matched energy level, which accelerated radiative recombination and charge injection balance for device operation. Consequently, the yellow CdZnSe-based QLEDs exhibited a peak external quantum efficiency of 23.7%, a maximum luminance of 686050cdm-2, and a current efficiency of 103.2cdA-1, along with an operating half-lifetime of 428523h at 100cdm-2. To the best of the knowledge, the luminance and operational stability of the device are found to be the highest values reported for yellow LEDs. Moreover, devices with electroluminescence (EL) peaks at 570-605nm exhibited excellent EQEs, surpassing 20%. The work is expected to significantly push the development of RGBY-based display panels and white LEDs.

Phase distribution management for high-efficiency and bright blue perovskite light-emitting diodes

Quasi-two-dimensional (quasi-2D) perovskite materials have attracted significant attention for application in light-emitting diodes (PeLEDs) due to their unique optical characteristics and extraordinary performance. The inherent multi-quantum well structure will generate a strong quantum confinement effect which is beneficial for the blue emission. However, the efficiency and stability of the quasi-2D blue PeLEDs lag behind their red and green counterparts, which prevents the further commercial application of the PeLEDs. The performance of quasi-2D blue PeLEDs was limited on account of the inefficient phase distribution management, which causes an inefficient energy transfer and severe non-radiative recombination. Herein, we employ guanidine thiocyanate (GASCN) as the pre-deposited film at the bottom of the perovskite film to manage the phase distribution of the PBA2Csn−1PbnBr3n+1 quasi-2D perovskite film (where n is the number of [PbBr6]4- sheets, and PBA is phenylbutylammonium). The pre-deposited GASCN can not only inhibit the small n-phase (i.e., n = 1: PBA2PbBr4, and n = 2: PBA2CsPb2Br7) but also avoid the undesired emission redshift from the over-growth of the large n-phase as well as passivate defects of the quasi-2D perovskite film, which accelerates energy transfer efficiently, strengthens the carrier transport, and enhances the luminous efficiency. As a result, the optimized device demonstrated the highest external quantum efficiency (EQE) of 16.40% and a maximum luminance of 8290 cd m−2. This strategy provides a new pathway to accurately manage phase distribution of quasi-2D perovskite achieving the high efficiency in blue PeLEDs.

Efficient and Bright Organic Radical Light-Emitting Diodes with Low Efficiency Roll-Off.

Organic radicals have been of interest due to their potential to replace nonradical-based organic emitters, especially for deep red/near-infrared (NIR) electroluminescence (EL), based on the spin-allowed doublet fluorescence. However, the performance of the radical-based EL devices is limited by low carrier mobility that causes a large efficiency roll-off at high current densities. Here, we report highly efficient and bright doublet EL devices by combining a thermally activated delayed fluorescence (TADF) host that supports both electron and hole transport and a tris(2,4,6-trichlorophenyl)methyl-based radical emitter. Steady-state and transient photophysical studies reveal the optical signatures of doublet luminescence mechanisms arising from both host and guest photoexcitation. The host system presented here allows balanced hole and electron currents, and we report a high maximum external quantum efficiency (EQE) of 17.4% at 707nm peak emission with substantially improved efficiency roll-off: over 70% of the maximum EQE (12.2%) is recorded at 10mA cm-2 , and even at 100mA cm-2 , nearly 50% of the maximum EQE (8.4%) is maintained. Charge recombination is primarily at the radical guest sites, but there is evidence from magneto-EL for host recombination and later energy transfer to the radical guest. We consider this is an important step to the practical application of organic radicals to NIR light-emitting devices. This article is protected by copyright. All rights reserved.

Electronic Properties of Zn2V(1-x)NbxN3 Alloys to Model Novel Materials for Light-Emitting Diodes.

We propose the Zn2V(1-x)NbxN3 alloy as a new promising material for optoelectronic applications, in particular for light-emitting diodes (LEDs). We perform accurate electronic-structure calculations of the alloy for several concentrations x using density-functional theory with meta-GGA exchange-correlation functional TB09. The band gap is found to vary between 2.2 and 2.9 eV with varying V/Nb concentration. This range is suitable for developing bright LEDs with tunable band gap as potential replacements for the more expensive Ga(1-x)In(x)N systems. Effects of configurational disorder are taken into account by explicitly considering all possible distributions of the metal ions within the metal sublattice for the chosen supercells. We have evaluated the band gap's nonlinear behavior (bowing) with variation of V/Nb concentration for two possible scenarios: (i) only the structure with the lowest total energy is present at each concentration and (ii) the structure with minimum band gap is present at each concentration, which corresponds to experimental conditions when also metastable structures are presents. We found that the bowing is about twice larger in the latter case. However, in both cases, the bowing parameter is found to be lower than 1 eV, which is about twice smaller than that in the widely used Ga(1-x)In(x)N alloy. Furthermore, we found that both crystal volume changes due to alloying and local effects (atomic relaxation and the V-N/Nb-N bonding difference) have important contributions to the band gap bowing in Zn2V(1-x)NbxN3.

Ionic liquid alkyl chain regulated highly stable and luminescent silica-coated perovskite quantum dots for bright white light-emitting diodes

Silica-coated perovskite quantum dots (QDs), which exhibit exceptional photophysical properties, hold great promise for various optoelectronic applications. Nonetheless, the issue of insufficient stability poses a significant challenge to their continued advancement and widespread adoption. Herein, we present a novel approach for the synthesis of silica-coated CH3NH3PbBr3 (CH3NH3 = MA) QDs with exceptional stability and luminescence, which utilized hydrophobic ionic liquids (ILs) with unlike alkyl chain lengths as surface ligands. As the alkyl chain length of the hydrophobic ILs increased, we observed a blue-shift in the wavelength and a reduction in the time required to reach maximum fluorescence for the silica-coated perovskite QDs. It not only effectively prevents QD aggregation but also accelerates the formation rate of the SiO2 shell. The introduction of ILs generated the enhancement of photoluminescence quantum yield (PLQY) from 85% for the pristine sample to 92.83% for ILs treated C16-QDs@SiO2. Furthermore, the stability of the ILs-treated C16-QDs@SiO2 was notably enhanced, with the fluorescence intensity retaining 80.5% after 40 days of storage. The as-prepared white light emitting diode (LED) displayed a high color rendering index (CRI) of 75.3 and a correlated color temperature (CCT) of 7529 K. This work provides an alternative strategy to solve the challenging stability issue of silica-coated perovskite QDs and promote the silica-coated perovskite QDs to the practical application in solid-state LEDs.

Manipulation of Charge Dynamics for Efficient and Bright Blue Perovskite Light-Emitting Diodes with Chiral Ligands.

Perovskite light-emitting diodes (PeLEDs) emerge as a promising class of optoelectronic devices for next-generation displays and lighting technology. However, the performance of blue PeLEDs lags far behind that of their green and red counterparts, including the unachieved trade-off between high efficiency and high luminance, severe efficiency roll-off, and unsatisfactory power efficiency. Here, a multi-functional chiral ligand of L-phenylalanine methyl ester hydrochloride is strategically introduced into quasi-two-dimensional perovskites, which can effectively passivate defects, modulate the phase distribution, improve photoluminescence quantum yield, guarantee high-quality film morphology, and enhance charge transport. Furthermore, ladder-like hole transport layers are established, boosting charge injection and balance. The resultant sky-blue PeLEDs (the photoluminescence peak is 493nm, and the electroluminescence peak is 497nm) exhibit an external quantum efficiency of 12.43% at 1000cd m-2 and a record power efficiency of 18.42lm W-1 , rendering that the performance is among the best blue PeLEDs. This article is protected by copyright. All rights reserved.

Fabrication of Highly Luminescent Quasi Two-Dimensional CsPbBr3 Perovskite Films in High Humidity Air for Light-Emitting Diodes.

Perovskite light-emitting diodes (LEDs) have attracted extensive attention in recent years due to their outstanding performance and promise in lighting and display applications. However, the fabrication of perovskite LEDs usually requires a low-humidity atmosphere, which is unfavorable for industrial production. Herein, we report an effective strategy to fabricate highly luminescent quasi two-dimensional CsPbBr3 perovskite films in an ambient atmosphere with a humidity up to 60%. We reveal that the hole transport layer (HTL) plays a significant role in the morphology and optical properties of the perovskite films. Using hydrophobic self-assembled monolayer materials as HTLs can remarkably improve the quality of the perovskite films processed in high humidity air. The resultant perovskite LEDs show reduced leakage current and significantly enhanced performance. Furthermore, surface treatment is conducted to prevent water invasion and promote radiative recombination in perovskite films and LEDs. Eventually, the perovskite LEDs exhibit bright green emission with an external quantum efficiency of 4.87%. The present work provides a feasible pathway to overcome the humidity limitation for obtaining bright perovskite films and LEDs, which would contribute to further reducing the fabrication cost of perovskite LEDs and promoting their applications.

Bright and Efficient Light-Emitting Devices Based on 2D Transition Metal Dichalcogenides.

2D monolayer transition metal dichalcogenides (TMDCs) show great promise for the development of next-generation light-emitting devices owing to their unique electronic and optoelectronic properties. The dangling-bond-free surface and direct-bandgap structure of monolayer TMDCs allow for near-unity photoluminescence quantum efficiencies. The excellent mechanical and optical characteristics of 2D TMDCs offer great potential to fabricate TMDC-based light-emitting diodes (LEDs) featuring good flexibility and transparency. Great progress has been made in the fabrication of bright and efficient LEDs with varying device structures. In this review, the aim is to provide a comprehensive summary of the state-of-the-art progress made in the construction of bright and efficient LEDs based on 2D TMDCs. After a brief introduction to the research background, the preparation of 2D TMDCs used for LEDs is briefly discussed. The requirements and the corresponding challenges to achieve bright and efficient LEDs based on 2D TMDCs are introduced. Thereafter, various strategies to enhance the brightness of monolayer 2D TMDCs are described. Following that, the carrier-injection schemes enabling bright and efficient TMDC-based LEDs along with the device performance are summarized. Finally, the challenges and future prospects regarding the accomplishment of TMDC-LEDs with ultimate brightness and efficiency are discussed.

Solvent-free synthesis of oil-soluble fluorescent carbon dots for bright photoluminescent and electroluminescent light-emitting diodes

Fluorescent carbon dots (CDs) have attracted great attention in multidisciplinary fields due to their distinctive advantages of tunable emission, low toxicity and abundant raw materials. However, it is still a big challenge to effectively applicate these CDs in electroluminescent light-emitting diodes (LEDs) due to their poor oil solubility and easy aggregation-induced quenching. Herein, an oil-soluble fluorescent CDs is designed and synthesized using triphenylamine and 4-iodophenyldiphenylamine as precursors through a solvent-free reaction. The obtained CDs (TPA-CDs) display an emission peak at 551 nm with good oil-solubility in different organic solvents. Therefore, TPA-CDs can be used as the host material of emission layer to prepare monochromatic electroluminescent LEDs with a maximum luminance of 227 cd·m−2 and as guest material in PVK to demonstrate white light electroluminescent LED with a maximum luminance of 1503 cd·m−2. This CDs can also be mixed well with oil soluble resin to easily assemble photoluminescent devices with a high luminous efficiency of 17.1 lm·W−1. This is the first example that solvent-free synthesized CDs are used for both photoluminescent and electroluminescent devices.

Perovskite Nanocrystals Protected by Hermetically Sealing for Highly Bright and Stable Deep-Blue Light-Emitting Diodes.

Metal-halide perovskite nanocrystals (NCs) have emerged as suitable light-emitting materials for light-emitting diodes (LEDs) and other practical applications. However, LEDs with perovskite NCs undergo environment-induced and ion-migration-induced structural degradation during operation; therefore, novel NC design concepts, such as hermetic sealing of the perovskite NCs, are required. Thus far, viable synthetic conditions to form a robust and hermetic semiconducting shell on perovskite NCs have been rarely reported for LED applications because of the difficulties in the delicate engineering of encapsulation techniques. Herein, a highly bright and durable deep-blue perovskite LED (PeLED) formed by hermetically sealing perovskite NCs with epitaxial ZnS shells is reported. This shell protects the perovskite NCs from the environment, facilitates charge injection/transport, and effectively suppresses interparticle ion migration during the LED operation, resulting in exceptional brightness (2916cd m-2 ) at 451nm and a high external quantum efficiency of 1.32%. Furthermore, even in the unencapsulated state, the LED shows a long operational lifetime (T50 ) of 1192 s (≈20min) in the air. These results demonstrate that the epitaxial and hermetic encapsulation of perovskite NCs is a powerful strategy for fabricating high-performance deep-blue-emitting PeLEDs.

Eliminating Nanocrystal Surface Light Loss and Ion Migration to Achieve Bright Mixed-Halide Blue Perovskite LEDs

Blue light-emittin g diodes (LEDs) are important components for perovskite electroluminescence applications, which still suffer from insufficient luminescence efficiency and poor stability. In Cl/Br mixed perovskite NCs, surficial defects cause severe light failure and ion migration, the in-depth mechanism of which is also not clear. To gain insights into these issues, we employ the ligand post-addition approach for mixed Cl/Br NCs by using octylammonium hydrobromide (OctBr) ligands, which effectively decrease surficial light loss and block ion migration pathways. The passivated CsPbCl1.5Br1.5 NCs exhibit exceptional blue emission with 95% PLQY, and the electroluminescence spectra of LEDs are located at the initial positions at the initial states. The treated NC blue devices show a negligible color shift as the voltage increases, which proves that electric-field-driven ion migration is drastically suppressed. In addition, OctBr-treated CsPbCl1.5Br1.5 and CsPbClBr2 NC LEDs show high external quantum efficiencies of 2.42 and 3.05% for emission peaks at 456 and 480 nm, respectively. Our work identified the nature of NC surface defects and provided a surficial modification approach to develop high-performance and color-stable blue mixed-halide perovskite LEDs.