White Light-emitting Diodes Research Articles

Spectral studies of thermally stable Dy3+/Sm3+ co-doped Li2Ba5W3O15 phosphors for warm white LEDs

In the current study, a series of Li2Ba5W3O15: RE3+ (RE = Dy, Sm) [LBW:Dy3+/Sm3+] phosphors were prepared using a high-temperature solid-state method. X-ray diffraction, Scanning electron microscopy with energy-dispersive x-ray analysis scans showed that the crystal form was consistent with the standard LBW and comprised small irregularly shaped particles. Diffuse reflectance spectral (DRS) data was utilized to calculate the band gaps. Fluorescence study shows that LBW material doped with Dy3+ and Sm3+ yield distinct colors at 496 nm (blue) for Dy3+ and 582 nm (green-yellow), 612 nm (yellow), and 669 nm (red) for Sm3+ when excited by near-ultraviolet (336 nm) light. The observation of energy transfer between Dy3+ and Sm3+ ions play a role in modifying the luminescence of LBW:Dy3+/Sm3+ co-doped phosphors. With a constant excitation wavelength (λ Ex), different levels of activator doping lead to a change in the emission colors from their neutral white light to a deep orange-red region for LBW:Dy3+/Sm3+ phosphors. The decay curves demonstrate a decrease in lifetime with an increase in the concentration of activator ions (Sm3+). For D3S5 phosphor, the temperature-dependent photoluminescence characteristics were analyzed under λ Ex = 336 nm excitation. The results indicate excellent luminescence thermal stability with an activation energy of 0.16 eV at λ Ex = 336 nm. With its low color-correlated temperature and good thermal stability, the prepared phosphor sample shows potential as a solid-state emitting phosphor that can be used with UV chip stimulation for warm white LED applications.

Stable solvatochromic light-emitting diodes and their potential for color temperature adjustment of white LEDs

A viable technology for liquid phosphor-based light-emitting diodes (LEDs) with emission color tuneability is described. These devices are based on Tris(bipyridine)ruthenium(II) chloride but can be constructed from other similar metal coordination charge transfer complexes. The Frank-Condon excited state generated upon the absorption of blue (450 nm) pump photons has a large electric dipole moment due to intramolecular metal-to-ligand charge transfer from the ruthenium atom to one specific bipyridyl ligand. Polar solvents respond to the dipole field creating a solvatochromic shift that is solvent dependent. The devices were fully sealed in either a long path length or a short path length configuration. The latter encapsulating the luminescing medium in hollow silica spheres that can be easily applied like a slurry on top of InGaN/GaN LED dies. The devices were optically, thermally and environmentally stable. Also discussed is the possibility of using solvatochromic emitters for achieving color temperature tuneability in white LEDs.

White Light Emissive Eu(III) Complexes through Ligand Engineering and their Applications in Cool Near Ultraviolet White Light Emitting Diodes and Thermometer.

In pursuit of enhancing white light quality for SSLapplications, an attempt has been made to design novel imidazo-bipyridyl ligands as an ancillary ligand to obtain multiple emissions (mimic sunlight) in the Eu-complex. By strategically modifying the phenanthroline core with imidazo-bipyridyl incorporation with 1 or 2-Napthyl groups at the C1 position, the excitation spectral line is successfully shifted from Ultraviolet (UV) to near UV/visible spectrum (where the LED emission occurs). The ligands showed greenish blue emission in solid and solution. The analysis revealed that the energy transfer is incomplete, primarily attributed to the proximity of triplet state energy levels to the resonance level of Eu(III) ions as reflected in solvatochromism. These complexes exhibit a unique dual emissive behavior (emitting multi-color) including white light across various solvents. The fabricated white LED showed an excellent color rendering index (CRI ~93 %). Beyond lighting, this distinctive property opens avenues for temperature sensing ([Eu(DBM)31-Naph] shows the highest sensitivity of Sr = 10.97 %, and [Eu(DBM)32-Naph] shows the highest sensitivity of Sr = 5.5 % at 333K) and vapoluminescent studies. This research pioneers the development of these complexes as potential single-component materials for white LEDs, underlining their multifaceted utility in cutting-edge lighting and sensing technologies.

Progress in Research on White Organic Light-Emitting Diodes Based on Ultrathin Emitting Layers

White organic light-emitting diodes (WOLEDs) hold vast prospects in the fields of next-generation displays and solid-state lighting. Ultrathin emitting layers (UEMLs) have become a research hotspot because of their unique advantage. On the basis of simplifying the device structure and preparation process, they can achieve electroluminescent performance comparable to that of doped devices. In this review, we first discuss the working principles and advantages of WOLEDs based on UEML architecture, which can achieve low cost and more flexibility by simplifying the device structure and preparation process. Subsequently, the successful applications of doping and non-doping technologies in fluorescent, phosphorescent, and hybrid WOLEDs combined with UEMLs are discussed, and the operation mechanisms of these WOLEDs are emphasized briefly. We firmly believe that this article will bring new hope for the development of UEML-based WOLEDs in the future.

Unraveling the Defect‐Induced Spectral Tuning in a Ce‐Doped Garnet Solid‐Solution Phosphor

Unraveling the Defect‐Induced Spectral Tuning in a Ce‐Doped Garnet Solid‐Solution Phosphor

Modulation and Enhancement of Red Luminescence in Ca2GdSbO6: Eu3+ Phosphor by Co-Doping with Bi3.

The double perovskite structure of Ca2GdSbO6 as a fluorescent phosphor matrix material possesses a stable structure, making it an excellent candidate for a matrix material. In this study, single-doped Ca2GdSbO6: Eu3+ fluorescent phosphors and Bi3+ sensitized Ca2GdSbO6: Eu3+, Bi3+ fluorescent phosphor materials were synthesized using the high-temperature solid-state method. The luminescence of this phosphor is based on the 5D0→4F2 transition emission of Eu3+ ions, which occurs at 612nm. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL) spectra, high-temperature fluorescence spectra, and fluorescence decay lifetimes to study the phase structure, optical properties, crystal structure, and chemical purity of the samples. The performance of the single-doped phosphor was significantly improved by the addition of Bi3+ sensitizer. The luminescence intensity increased by nearly 100% compared to Ca2GdSbO6: Eu3+ phosphor, with a quantum efficiency increase of 124%. The thermal quenching activation energy was found to be 0.299eV, and the luminescence intensity remained at 70.3% of room temperature at 453K. These results indicate that the co-doping of Bi3+ has a modulation and enhancement effect on the luminescence of Ca2GdSbO6: Eu3+ red phosphor, showing great potential for application in near-ultraviolet-excited white LED devices.

Rational Design of Nitride Phosphor-In-Glass with Robust Stability and Photoluminescence Performance.

Phosphor-in-glass represents a promising avenue for merging the luminous efficiency of high-quality phosphor and the thermal stability of a glass matrix. Undoubtedly, the glass matrix system and its preparation are pivotal factors in achieving high stability and preserving the original performance of embedded phosphor particles. In contrast to the well-established commercial Y3Al5O12:Ce3+ oxide phosphor, red nitride phosphor, which plays a critical role in high-quality lighting, exhibits greater structural instability during the high-temperature synthesis of inorganic glasses. A telluride glass with a refractive index (RI = 2.15@615 nm) akin to that of nitride phosphor (∼2.19) has been devised, demonstrating high efficiency in photon utilization. The lower glass-transition temperature plays a crucial role in safeguarding phosphor particles against erosion resulting from exposure to high-temperature melts. Phosphor-in-glass retains 93% of the quantum efficiency observed for pure phosphor. The assembled white light-emitting diodes module has precise color tuning capabilities, achieving an optimal color rendering index of 93.7, a luminous efficacy of 80.4 lm/W, and a correlated color temperature of 5850 K. These outcomes hold potential for advancing the realm of inorganic package and high-quality white light illumination.

Atomic-level investigation of structure and formation process of Y3Al5O12 with super-high content of Ce emitting anomalous orange-red emissions

Ce-doped yttrium aluminum garnet (YAG:Ce, Y3Al5O12:Ce) is the most commonly used yellow phosphor in white light-emitting diodes. Recently, we found that (Y1–xCex)3Al5O12:Ce with a super-high content of Ce (x = 0.11–0.21) can be prepared by a polymerized complex method and exhibits anomalous orange–red emission. To understand the nature of this anomalous behavior from the atomic level, we applied high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and scanning transmission electron microscopy–energy dispersive X-ray spectroscopy (STEM-EDS), a state-of-the-art technique that enables analysis of the atomic-level elemental distributions of Al, Y, and Ce. STEM-EDS images on the atomic level were successfully obtained for YAG:Ce. It was found that Ce in Y site has spatially uneven for few nanometers. Ce–K edge extended X-ray absorption fine structure (EXAFS) analysis was also conducted, which revealed a high level of asymmetry around Ce. By combining the STEM-EDS and EXAFS results, a dynamic model for the red emission was proposed. STEM-EDS also revealed that CeO2 nanocrystals were firstly formed with low-temperature annealing and that the reaction of Y with the CeO2 nanocrystals subsequently yielded YAG:Ce, unlike in the conventional one-step high-temperature synthesis.

Meticulously designed red emission carbon dots as efficient and stable luminescent species for rapid latent fingerprint recognition and light emitting diodes

The preparation of carbon dots (CDs) emitting long wavelength has attracted more attentions due to their unique advantages in biological and optoelectronic fields, including the wide absorption, long PL lifetime and deep-tissue penetration. Herein, we prepare the nitrogen and sulfur co-doped red emission carbon dots (R-CDs) from the 2,4-diaminodiphenylamine (DDA) and thiourea via a solvothermal reaction, which exhibit reliable red emission at 613 nm and possess a high quantum yield (QY) of 34 %. Meanwhile, the structural analysis and theoretical calculation reveal that the sulfur doping from thiourea increases the nitrogen and oxygen content of CDs, leading to the red emission observed in R-CDs. Subsequently, we design an integrated fingerprints recognition system based on the R-CDs phosphors for the imaging of latent fingerprints (LFPs) and fast LFPs recognition, expanding the application of biometric identification and comparison technology based on fluorescence. Finally, we successfully apply the R-CDs into red and white light-emitting diodes, improving plant growth efficiency. As a result, this work provides a new in-depth insight of red emission CDs and expands the application in latent fingerprint recognition and light-emitting diodes.

White carbon dots with high quantum yield and multicolor carbon dots synthesized by the microwave method in one step

In the field of optics, carbon dots (CDs) have been extensively studied and have made rapid advancements in related fields, including bioimaging, optoelectronic devices and optical probes. However, it is difficult to efficiently synthesize high quantum yield (QY) white fluorescence CDs and multicolor CDs, which restricts their development in the field of optics. In this work, we chose formamide as the reaction solvent and used citric acid (CA) and 4-bromo-1,2-diaminobenzene to synthesize high-performance white fluorescent CDs20 with a QY of up to 87.5% and excellent stability (28 days). The reaction solvents (water, N,N-dimethylformamide and ethanol) were changed to obtain colorful CDs20 (orange, green and yellow) covering a broader visible spectrum via a microwave method. The solid model, which combines white fluorescent CDs20 and polyvinyl alcohol (PVA), exhibits strong white fluorescence as well as a solution state. To develop white-emitting diodes suitable for indoor use, a white CDs20 / PVA mixture with brilliant white fluorescence might be placed on ultraviolet (UV) chips (365 nm). The white LED had a high color purity (0.34, 0.25), excellent correlation color temperature (4250 K) and color rendering index (72.5). The results above show that white CDs have great promise for use in optical device fields.

Enhanced environmental stability and luminescence performance of CsPbI3 nanocrystals through SDS passivation and LEuH anchoring

CsPbI3 perovskite nanocrystals (NCs) have been identified as promising candidates for optoelectronic devices due to their low bandgap, wide absorption spectrum, and high color purity. However, their practical applications are limited by their vulnerability to transforming into the yellow non-perovskite phase in ambient conditions. In this study, we propose a novel approach to prepare highly stable black-phase CsPbI3 NCs by passivating them with sodium dodecyl sulfate (SDS) and anchoring them with flower-like layered europium hydroxide (LEuH). The addition of SDS to CsPbI3 NCs plays a crucial role in inhibiting defect formation by preventing the ligand from desorbing. Furthermore, LEuH, with its surface OH– groups, effectively anchors the CsPbI3 NCs onto its nanosheets, preventing their agglomeration. The resulting composite LEuH-SDS-CsPbI3 nanocomposites exhibit extraordinary environmental stability, maintaining their phase structure even after 60 days of storage under ambient conditions. Additionally, their photoluminescence quantum yield reaches an impressive 95 %. The exceptional luminescence performance of the LEuH-SDS-CsPbI3 nanocomposites opens up new possibilities for their application in optoelectronic devices. Furthermore, when used in white LEDs, these nanocomposites exhibit excellent luminescence efficiencies, further highlighting their potential for commercial utilization in the field.

Fluorescent nanocomposites of Ag nanoclusters grown in anionic polymer layers grafted to plastic substrate: Preparation, characterization and evaluation in Hg2+ sensing and white light generation

AbstractFluorescent noble metal nanoclusters (NCs) are emerging optical nanomaterials with properties similar to those of quantum dots. Their applications can be expanded by combining them with polymer matrices to obtain flexible and transparent light‐emitting nanocomposites. However, achieving highly fluorescent nanocomposites of this type remains challenging due to phase separation and aggregation of NCs in polymer hosts leading to a strong reduction in fluorescence efficiency. We address this key issue by covalently grafting a layer of a specifically selected matrix polymer onto a transparent plastic film and photochemically synthesizing the fluorescent metal NCs directly in the grafted layer. The surface‐grafted matrix polymer effectively captures the noble metal (Ag) ions, photo‐reduces them to atoms, acts as a capping ligand for the growing Ag NCs, and immobilizes them on the substrate surface. The Ag NCs were produced by both wet and dry synthesis, and effects of synthesis method, reaction time, and matrix polymer layer thickness on the fluorescence properties of the resulting nanocomposites were investigated and discussed. Importantly, the fluorescence intensity of these nanocomposite films is sensitive to submicromolar concentrations of aqueous Hg2+ that makes them useful as fluorescent sensing materials for selective and ultrasensitive detection of Hg2+ ions in water. Besides, the nanocomposite films obtained by the dry synthesis of NCs exhibit an intensive emission covering the whole green to red range of the visible spectrum and, hence, produce bright white light under illumination with a blue LED that makes them attractive as down‐conversion materials in one‐phosphor‐converted white LEDs.

Lead-free Perovskite with Distorted [InX6]3- Octahedron Induced by Organic Cation and Enhanced PLQY by Sb Doping.

In-based halide perovskites have attracted a lot of attention because of their unique broadband emission properties. Herein, a series of In-based hybrid perovskites of (H2MP)2InCl7·H2O (1), (H2EP)2InCl7·H2O (2), (H2MP)2InBr7·H2O (3), and (H2EP)2InBr7·H2O (4) were synthesized under the control of halogen ions and organic cations. 1, 2, and 4 exhibit obvious photoluminescence properties with peaks at 392, 442, and 652 nm, respectively. The effects of the different components on the crystal structure and photoluminescence properties are discussed by calculating the structural distortion of the [InX6]3- octahedron. The photoluminescence properties of 1 and 4 were significantly improved after Sb3+ doping with PLQY values of 57.12 and 41.53%. Finally, a white LED was successfully fabricated with the two doped compounds coated onto the 365 nm blue LED chip.

Simple Sol-Gel Protein Stabilization toward Rainbow and White Lighting Devices.

Fluorescent proteins (FPs) are heralded as a paradigm of sustainable materials for photonics/optoelectronics. However, their stabilization under non-physiological environments and/or harsh operation conditions is the major challenge. Among the FP-stabilization methods, classical sol-gel is the most effective, but less versatile, as most of the proteins/enzymes are easily degraded due to the need of multi-step processes, surfactants, and mixed water/organic solvents in extreme pH. Herein, sol-gel chemistry with archetypal FPs (mGreenLantern; mCherry) is revisited, simplifying the method by one-pot, surfactant-free, and aqueous media (phosphate buffer saline pH=7.4). The synthesis mechanism involves the direct reaction of the carboxylic groups at the FP surface with the silica precursor, generating a positively charged FP intermediate that acts as a seed for the formation of size-controlled mesoporous FP@SiO2 nanoparticles. Green-/red-emissive (single-FP component) and dual-emissive (multi-FPs component; kinetic studies not required) FP@SiO2 are prepared without affecting the FP photoluminescence and stabilities (>6months) under dry storage and organic solvent suspensions. Finally, FP@SiO2 color filters are applied to rainbow and white bio-hybrid light-emitting diodes featuring up to 15-fold enhanced stabilities without reducing luminous efficacy compared to references with native FPs. Overall, an easy, versatile, and effective FP-stabilization method is demonstrated in FP@SiO2 toward sustainable protein lighting.

Biomass and Ginsenosides Content of Ginseng Sprouts upon Exposure to Several White LED Lights with Different Correlated Color Temperatures and Color Rendering Indexes

Biomass and Ginsenosides Content of Ginseng Sprouts upon Exposure to Several White LED Lights with Different Correlated Color Temperatures and Color Rendering Indexes

A Brief Synthesis Methods and Luminescence Development of Rare Earth Activated Borophosphate Phosphor Materials

A Brief Synthesis Methods and Luminescence Development of Rare Earth Activated Borophosphate Phosphor Materials

Luminescent Perovskite-Cross-Linked Polymer with Low Shrinkage and Excellent Stability.

When organic cross-linked polymers are combined with metal halide perovskite nanocrystals (PNCs) for realizing luminescent perovskite-polymer display materials, the stability of PNCs is enhanced and their shrinkage is suppressed. This work presents a feasible strategy for preparing CsPbBr3 nanocrystals (NCs) within a polydicyclopentadiene (PDCPD) thermosetting cross-linked resin matrix simultaneously via a one-step reaction. The obtained PDCPD@PNCs composite exhibits narrow peak half-widths (15-20 nm), high light transmittance (80%), low curing volume shrinkage (1.4%), tunable tensile properties, excellent stability, and a photoluminescence quantum yield (PLQY) of 44.3%. The composite material exhibits long-term stability in water, acid, and base solutions for over 90 days, with the PL intensity being maintained at over 90%. Furthermore, the composite is highly resistant to polar organic solvents owing to the insolubility imparted by cross-linking. White LEDs (WLED) fabricated using the as-prepared composite demonstrate excellent potential as light sources in optical devices.

Stimuli-induced modulation of white light emission in colloidal polymer particles: Design of chemosensors and dynamic chromism toward unclonable patterning and its classification based on machine learning

Stimuli-responsive light-emitting materials have gained significant attention due to their potential applications in optoelectronic devices, chemosensors, anticounterfeiting inks, and unclonable encryption. Coumarin-containing fluorescent polymer particles with light-, pH-, and thermo-responsiveness were prepared by distillation-precipitation polymerization of hydroxyethyl methacrylate and 2-(dimethylamino)ethyl methacrylate. White light emission was observed by physical incorporation of hydroxyl-functionalized spiropyran (SPOH) into the colloidal polymer particles in a certain ratio of the colloidal polymer particles and SPOH content. The white light emission was obtained by modulating pH and temperature to finely tune the Förster resonance energy transfer process and cover the entire visible spectra from the emissive lights. This phenomenon was successfully used to prepare pH sensors, dynamic anticounterfeiting inks, unclonable patterning, and also white light-emitting colloids, films, coatings, and diodes. As an example, a white light-emitting diode was fabricated using the SPOH-doped colloidal polymer particles in poly(vinyl alcohol) matrix having Commission Internationale del'Eclairage color coordinates of (0.31, 0.33). Dynamic chromism and preparation of randomly distributed blue, red, and white light-emitting patterns are examples of advanced anticounterfeiting and encryption methods that were generated via the prepared low-cost environmentally friendly waterborne ink. For the authentication purpose of the unclonable patterns, the classification algorithms were designed based on machine learning to classify the true patterns from the false ones.

Unveiling the Cultivation of Nostoc sp. under Controlled Laboratory Conditions

Cyanobacteria, photoautotrophic Gram-negative bacteria, play a crucial role in aquatic and terrestrial environments, contributing significantly to fundamental ecological processes and displaying potential for various biotechnological applications. It is, therefore, critical to identify viable strains for aquaculture and establish accurate culture parameters to ensure an extensive biomass supply for biotechnology purposes. This study aims to establish optimal laboratory batch culture conditions for Nostoc 136, sourced from Alga2O, Coimbra, Portugal. Preliminary investigations were conducted to identify the optimal culture parameters and to perform biomass analysis, including protein and pigment content. The highest growth was achieved with an initial inoculum concentration of 1 g.L−1, using modified BG11 supplemented with nitrogen, resulting in a Specific Growth Rate (SGR) of 0.232 ± 0.017 μ.day−1. When exposed to white, red, and blue LED light, the most favourable growth occurred under a combination of white and red LED light exhibiting an SGR of 0.142 ± 0.020 μ.day−1. The protein content was determined to be 10.80 ± 2.09%. Regarding the pigments, phycocyanin reached a concentration of 200.29 ± 30.07 µg.mL−1, phycoerythrin 148.29 ± 26.74 µg.mL−1, and allophycocyanin 10.69 ± 6.07 µg.mL−1. This study underscores the influence of light and nutrient supplementation on the growth of the Nostoc biomass.

Effects of light-emitting diodes on the morphology and accumulation of glucosinolates, carotenoids and phenolic acids in red kale sprouts

Kale (Brassica oleracea var. acephala) has gained popularity as a nutritious and phytochemical-rich vegetable. This study has investigated the effects of three LED treatments (white, blue, and red) on the accumulation of secondary metabolites in kale sprouts. Ten DAS, the kale sprouts were harvested, and growth measurements were measured. Furthermore, selected sprouts were stored at -80 °C for further biochemical analysis, namely, phenolic acids, glucosinolates, and carotenoids. Sprouts irradiated with red LED light showed the best SL, RT, and FW values. For total GSLs, we found that kale sprouts irradiated with white LED lights showed the best results (41.59±0.41 μmol/g DW). Among the aliphatic GSLs, we found that progoitrin presented the best results under blue LED light (17.93±0.49 µmol/g DW), and among the indolic GSLs, glucobrassicin showed the best results under white and red LED light. The highest concentration of total carotenoids was found in kale sprouts under white LED light exposure (3341.27±206.96 μg/g DW). Individually, β-carotene was observed in high concentration under white LED light (1935.13±87.21 μg/g DW). Among the PAs, chlorogenic acid was found in the highest concentration in the treatments under white LED light (45.78±0.73 µg/g DW). In general, kale sprouts irradiated with white LED light showed high contents of GSLs, carotenoids, and PAs. Regarding morphological characteristics, kale sprouts under red LED light showed the most promise. This research offers a valuable approach to enhancing the phytochemicals found in kale sprouting.