Chromaticity Coordinates Research Articles

Sol-gel synthesis of LaFeO3 perovskite oxide for distinct ridges detection of level II and III latent fingerprints

Latent fingerprints are considered a primary source of best reference for personal identification in criminal investigations. However, poor resolution, less background hindrance, and sensitivity over fingerprint ridges are often problems in fingerprint development. To address these issues, special care is required by developing new fluorescence materials. As a result, this effort was made to synthesize lanthanum ferrite (LaFeO3) fluorescent nano perovskite oxide by the sol–gel method using glycine as fuel, to detect three (I, II, and III) levels of fingerprints. In addition, the absorption spectrum was recorded in a dispersed medium, and dual peaks at 329 and 406 nm in visible regions were obtained, followed by the photoluminescence spectra that showed a broad peak at 527 nm with chromaticity coordinates. Powder X-ray diffraction confirms the synthesized LaFeO3 orthorhombic phase with a crystallite size of 54 nm, and the morphology of LaFeO3 was found to be highly monodisperse. X-ray photoelectron spectroscopy confirmed that La has + 3 with Fe + 3 oxidation states, and Infrared spectroscopic techniques revealed all functional groups were present uniformly. The powder dusting method was applied on various porous and non-porous surfaces, revealing distinct ridges of fingerprints without background hindrance and with precise sensitivity; this proves LaFeO3 is suitable for forensic science.

Host Engineering of Deep‐Blue‐Fluorescent Organic Light‐Emitting Diodes with High Operational Stability and Narrowband Emission

AbstractThe realization of highly operationally stable blue organic light‐emitting diodes (OLEDs) is a challenge in both academia and industry. This paper describes the development of anthracene–dibenzofuran host materials, 2‐(10‐(naphthalen‐1‐yl)anthracen‐9‐yl)naphtho[2,3‐b]benzofuran (Host 1) and 2‐(10‐([1,1′‐biphenyl]‐2‐yl)anthracen‐9‐yl)naphtho[2,3‐b]benzofuran (Host 2), namely for use in the emissive layer of an OLED stack. A multiple‐resonance thermally activated delayed serves as the blue fluorescence emitter and exhibits an initial luminance of 1000 cd m−2 and long operational stability (i.e., time to decay to 90% of initial luminance) of 249 h. Furthermore, a deep‐blue OLED with an optimized top‐emitting architecture with a high current efficiency of 154.3 cd A−1, is fabricated and calibrated to a Commission International de l’Éclairage y chromaticity coordinate of 0.048. Moreover, the emission spectrum of this OLED has a narrowband peak at 476 nm with a full width at half maximum (FWHM) of 16 nm. This work provides valuable insights into the design of anthracene‐based host materials and highlights the importance of host optimization in improving the operational stability of OLEDs.

Study on the properties of Sm3+-Doped CaTbAl3O7 phosphors

New single phase and adjustable emission phosphors have attracted a lot of attention because of the good luminous properties. In this work, Sm3+ doped CaTbAl3O7 phosphors are prepared in air by solid-state method. The crystal structure, concentration dependent spectra, lifetimes, and luminescence properties are investigated. Because of the 4f8 → 4f75d1 and 4f → 4f transitions of Tb3+ ion, host (CaTbAl3O7) shows an excitation spectrum in the range of 220–520 nm under monitored at 544 nm and emits yellow-green light under excitation 248, 284, and 368 nm due to the 5D4 → 7FJ (J = 0, 1, 2, 3, 4, 5, and 6) transitions of Tb3+ ion. CaTbAl3O7:Sm3+ under monitored 598 nm contains the excitation spectral peaks of both CaTbAl3O7 and Sm3+ ion. With excitation at 368 nm, CaTbAl3O7:Sm3+ glows orange-red light, its PL spectrum has both host (CaTbAl3O7) and Sm3+ ion contributing, and the chromaticity coordinates are about (0.5499, 0.4351). Under excitation 402 nm, the red-orange emission of CaTbAl3O7:Sm3+ is only the contribution of Sm3+ ion and the chromaticity coordinates are about (0.5823, 0.4168). The energy transfer process from Tb3+ in host (CaTbAl3O7) to Sm3+ ions can be confirmed via the spectral properties. We explain the luminous mechanism of CaTbAl3O7:Sm3+ by the energy level diagrams of Tb3+ and Sm3+.

Transcription of Customized Circularly Polarized Luminescence from Enantiomeric Metal–Organic Framework to Carbon Dots

AbstractChiral carbon dots (CDs) with circularly polarized luminescence (CPL) are one of the most dynamic areas of modern science. However, the design, preparation, and ambiguity mechanism of solid‐state CPL‐active CDs remains a formidable challenge. Herein, for the first time, CDs with customized chiroptical activities in the solid state, especially CPL, are transcribed from chiral metal–organic framework (CMOFs) via a bottle‐around‐ship strategy. Within these CMOFs⊃CDs assemblies, CDs inherited the chirality of the host CMOFs through host–guest interactions, which is revealed by density functional theory (DFT) simulations and experimental results, and amplified the luminescence dissymmetry factor (glum) by effective artificial chiral light‐harvesting systems. Impressively, CMOFs⊃CDs in pairs generated color‐tunable CPL and white CPL with chromaticity coordinates of (0.32, 0.32). Furthermore, benefiting from excellent processability, as luminescent coatings and 3D printing inks, a white circularly polarized light‐emitting diode, and an extended 3D model “light bulb” featuring white CPL are successfully fabricated, respectively. This strategy paves a new avenue for the synthesis and advanced application of solid‐state CPL‐active CDs‐based materials.

Hydrothermal syntheses, structures and photophysical properties of two lanthanide isonicotinic acid complexes

Two rare earth isonicotinic acid compounds [Y(HIA)2(H2O)4(NO3)](2NO3) ((1); HIA = isonicotinic acid) and [LaHg3Cl8(HIA)4] nnCl (2) were reported. Compound one features an isolated (0-D) structure, while compound two has a two-dimensional (2-D) structure. The rare earth ions are coordinated by eight oxygen atoms to display a square antiprismatic REO8 geometry. Compound one shows blue photoluminescence and it has CIE chromaticity coordinates of 0.2332 and 0.3104. The CCT of compound 1 is 13755 K. Compound two exhibits green photoluminescence and it has CIE chromaticity coordinates of 0.3663 and 0.6184. The CCT is 4997 K. Their band gaps are 2.86 and 3.12 eV.

Investigation on luminescent characteristics of Tb3+/Dy3+co-doped boro-phosphate glass for cool white LED and radiation shielding applications

The Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb) was produced (40 B2O3 + 39P2O5 + 5 Al2O3 + 5 NaF + 10 ZnO + 0.5 Tb2O3 + 0.5 Dy2O3) using melt-quenching technique. X-ray diffraction measurements, Raman, and Fourier Transform Infrared were used to evaluate the structural behavior of the prepared glass. Powder-XRD spectra, in the 10–90° range showed that the prepared glass was amorphous. FTIR analysis reveals that the network contains a variety of structural groups, including B-O-B, BO4, BO, P-O, PO2, P-O-B, and PO4 units. The UV–visible diffuse reflectance spectroscopy was used to record and study the optical linear properties of Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb). The photoluminescence excitation peak was obtained at 348 nm. The emission peaks were located at 484 nm (4F9/2 → 6H15/2 → blue), 576 nm (4F9/2 → 6H13/2 → yellow), and 662 nm (4F9/2 → 6H11/2 → red). Tb3+ ions are located at 412 nm (5D3 → 7F5), 441 nm (5D3 → 7F4), 546 nm (5D4 → 7F5), and 625 nm (5D4 → 7F3). The result of CIE 1931 chromaticity coordinates indicate that the prepared glass is suitable material for cold white light emitting diode applications due to its color coordinates x = 0.3106 and y = 0.3240 and correlated color temperature (CCT) values about 6768 K. The gamma-ray parameters such as half-value layer (HVL), mass attenuation coefficient (μ/ρ), mean free path (MFP), and effective atomic number (Zeff) of the BPANZDyTb glass were studied using Phy-X software. The results of the gamma-ray parameter show that the Dy3+ ions and Tb3+ ions co-doped BoroPhosphate glass is an appropriate material for radiation shielding applications.

Structural, morphological, optical and down-conversion studies of NaLaMgTeO6:Dy3+ single phase phosphor for white light emitting applications and solar spectral converter for photovoltaic applications

Researches on rare earth activated phosphors in solid state lighting and enhancement in efficiency of solar cells pave attention to develop efficient phosphor materials. In the present work, Dy3+ doped NaLaMgTeO6 phosphors are synthesized using solid state reaction method. The structural studies using XRD analysis confirmed the successful formation of the compound. SEM analysis reveals that the particles are closely packed, which in turn exhibit intense luminescence intensity due to low scattering and high packing density. Elemental configuration were analyzed using EDS analysis. FTIR analysis revealed the vibrational bands of the host matrix. Optical energy bandgap was calculated using DRS spectra. The luminescence characteristics of the samples were investigated using excitation and emission spectra. Upon most intense 351 and 388 nm excitation, sharp yellow emission peak at 572 nm dominates blue emission at 478 nm, further reveals that Dy3+ ions occupy low symmetry site in the host lattice. The optimum concentration of Dy3+ in the present host is x = 0.04 mol and concentration quenching is due to dipole-quadrupole interaction of adjacent Dy3+ ions. The thermal quenching phenomenon is studied using temperature dependent photoluminescence analysis. The CIE chromaticity coordinates and CCT values conclude NaLaMgTeO6:Dy3+ phosphors are good candidate for cool near-white light emitting materials for outdoor illumination. The study on solar spectral response and down-conversion property of the synthesized phosphor demonstrate its applicability as solar spectral converters in solar cell applications.

CsPb(Br/Cl)3-Sm3+ codoped glasses for optical temperature sensing in FIR and chromatic coordinate modes

We have fabricated Sm3+ doped glasses, CsPb(Br/Cl)3 quantum dots (QDs) glasses and CsPb(Br/Cl)3-Sm3+ codoped glasses by melt-quenching and subsequent heat treatment for optical temperature sensing. Photoluminescence (PL), photoluminescence excitation (PLE) spectra and PL decay have been measured. Two CsPb(Br/Cl)3-Sm3+ samples with different PL peaks of QDs at 486 nm and 503 nm have been studied for fluorescence intensity ratio (FIR) and chromatic coordinate sensing. The CsPb(Br/Cl)3 QDs and Sm3+ ions exhibit distinguished spectral components and they are dynamically independent. PL intensity of QDs rapidly decreases with temperature, whereas PL intensity of Sm3+ slowly decreases with temperature. PL intensity of Sm3+ ions and CsPb(Cl/Br)3 QDs have been independently fitted. Then, FIR sensing has been studied. The different variation in PL intensity with temperature for Sm3+ and CsPb(Cl/Br)3 leads to the change of luminescent color and chromatic coordinate. The chromatic coordinate sensing has also been studied. Absolute sensitivity (Sa) and relative sensitivity (Sr) have been analyzed for both FIR and chromatic coordinate sensing. Compared with the chromatic coordinate mode, FIR mode has the larger Sa and Sr. But the chromatic coordinate method is more convenient for application, which does not require separating two spectral components. Both FIR and chromatic coordinate sensing modes show outstanding temperature cycling characteristics.

White afterglow achieved in Eu2+, Ce3+, Dy3+co-doped LiSr4(BO3)3 phosphor

In prior study by our team, orange-yellow afterglow was observed in Eu2+ and Dy3+ co-doped LiSr4(BO3 )3 phosphor due to the emission from Eu2+ center. In this study, further incorporation of Ce3+into the phosphor lead to the observation of white afterglow due to the mixed result of blue light from Ce3+ and orange-yellow light from Eu2+ centers. Upon ultraviolet excitation, the phosphor displays a spectrum characterized from blue emission of Ce3+ at 462nm and orange-yellow emission of Eu2+ at 632nm. Fine-tuning the concentration of Ce3+ enabled the realization of white luminescence in LiSr4(BO3)3: Eu2+, Ce3+ and Dy3+phosphor with chromaticity coordinates of (0.3979, 0.2939). The photoluminescence intensities of the samples could be modulated by incorporating varying amounts of Ce3+ ions, with a critical quenching concentration identified with 0.16 Ce3+. White afterglow is also observed after the removal of the light illumination due to the existence of suitable electron traps with optimal trap depth created by the co-doped Dy3+. The underlying mechanism proposes that the white afterglow is generated by the mixed lights of blue and orange-yellow that are created by the recombination of heat-released electrons from the trap centers with pre-existing holes in the Ce and Eu emission sites.

Spectroscopic investigation of co-formers on Dy3+ ions activated Barium comprised zinc borate glasses for enhancing the solid-state laser applications

The purpose of the existing research is to analyze the luminescence behavior on a set of different co-formers involved Dy3+ ions activated Barium comprised zinc borate glasses fabricated through the utilization of usual melt quenching technique with a glass composition of 64B2O3+20ZnF2+15BaO+1Dy2O3 & 44B2O3+20A+20ZnF2+15BaO+1Dy2O3 (where A = 0, P2O5, TeO2, Bi2O3). Their structural, optical, luminescence and decay behavior were scrutinized by several respective characterization techniques. Some of the physical properties were calculated by utilizing the corresponding formulae. Besides, the bonding parameter and oscillator strength estimation alongside Judd-Ofelt parameter are also computed to find out the radiative properties from luminescence spectra. From these analyses, ionic nature of the glass network was confirmed. The spectroscopic intensity parameter follows the tendency Ω2>Ω6>Ω4. This higher value of Ω2 is owing to the larger oscillator strength value and signalizing that Dy3+ ions are completely doped into the glass network. Among all the as- quenched samples, BZfBaT:Dy glass possesses high stimulated emission cross-section and holds high optical gain width value which implies that the glass is a perfect candidate intended for laser utilization. By utilizing its emission spectra, the colour chromaticity coordinates (x, y), colour purity, colour correlated temperature (CCT), and Y/B intensity ratio were investigated by means of CIE 1931 diagram and confirmed the light emitting capability. Decay curve displays well-fitting with the exponential fit and the efficiency (ɳ) for the BZfBaP:Dy glass is found to be 61 % and possesses high optical gain signalizing that the material is a perfect choice for optoelectronic applications.

Synthesis and photoluminescent spectroscopic analysis of lanthanum (III) coordinated with 1,10-Phenanthroline: A study of its thermally stable behavior

A blue-emitting phosphor designed by lanthanum (III) coordinated with two 1,10-Phenanthroline and three nitrate ligands, [La(Phen)2(NO3)3], was obtained by an effective and simple precipitation method. Fourier transform infrared spectroscopy (FTIR) and powder X-ray diffraction (PXRD) revealed the coordination modes in the compound and the chemical structure, crystallizing in a monoclinic system in the C2/c space group. The luminescence properties, absolute quantum yield (ϕ), and luminescence lifetime decay (τ) were determined by photoluminescence spectroscopy. Under a 350 nm excitation, the sample presents three emission bands corresponding to the π* → π transitions belonging to the organic ligand. The luminescence lifetime (τ) was determined through a monoexponentially fit, obtaining a value of 5616 ns. The [La(Phen)2(NO3)3] complex exhibits an absolute quantum yield of 3 % with the same excitation conditions. In addition, the photometric analysis shows that the luminescent response to a 350 nm excitation is that of a blue-emitting high-purity phosphor with 96 % and chromatic coordinates of 0.15, 0.05. The temperature-dependent luminescence properties revealed considerable thermal stability in the 20–150 °C range with a signal loss of 47 % and an activation energy of thermal quenching (ΔE) of 0.13 eV, the first value reported for a lanthanum complex based on 1,10-Phenanthroline.

Exploring inorganic phosphors: basics, types, fabrications and their luminescence properties for LED/WLED/displays

Abstract The utilization of phosphors in lighting and display applications has garnered significant attention due to their unique luminescent properties and versatile crystal structures. This review article comprehensively examines recent advances in the synthesis, characterization, and applications of nitride and sulfide phosphors. This article addresses various phosphor crystal structures, including perovskite, garnet, nitride sulfide, fabrications strategies, and their impact on the optical and electronic properties. Furthermore, the review highlights the role of doping and activator ions in tailoring the emission characteristics of nitride and sulfide phosphors, enabling precise control over color rendering and efficiency. Additionally, the article also discusses emerging trends in phosphor technology, such as the development of novel synthesis methods and the integration of phosphors into next-generation lighting and display devices. The basic properties of phosphor materials like CRI, CIE chromaticity coordinates, quantum efficiencies are well discussed. Overall, this article provides valuable insights into the current state of research and future directions in the field of phosphors offering potential avenues for further advancements in lighting and display technologies.

A novel Na2Ca2Si3O9: Tb3+ glass ceramic with high luminescence efficiency and robust thermal stability for white LED lighting application

Given the increasing demand for white light emitting diode (WLED) lighting devices marked by high color rendering indices (CRI) and exceptional thermal stability, there is a burgeoning interest in developing emitters with enhanced performance. Rare earth (RE) ion-activated glass ceramics (GCs) have garnered significant attention due to their outstanding physicochemical and thermal stability, alongside their high luminescence efficiency. In this study, the GCs doped with Tb3+ ions in the Na2O-CaO-SiO2 system matrix were synthesized, incorporating Na2Ca2Si3O9 nanocrystals averaging less than 100 nm in size. Notably, these GC materials demonstrated superior luminescence efficiency in the green light emission under the irradiation of 376 nm light compared to the parent glass. A comprehensive analysis of fluorescence spectra revealed an impressive internal quantum efficiency of 87.34 % for this Tb3+-doped GC. Furthermore, the GC retained 90 % and 84 % of the initial luminescence intensity at 150 °C and 200 °C in comparison to the luminescence level at room temperature, showcasing exceptional resistance to fluorescence thermal quenching. Verification experiments utilized UV LED chip, (Sr, Ca)AlSiN3: Eu2+ red phosphor, BaMgAl10O17: Eu2+ blue phosphor, and Tb3+-doped GC to encapsulate the WLED device, achieving a remarkable CRI of 92, CIE chromaticity coordinates (0.3547, 0.3361), and a correlated color temperature (CCT) of 4550K. In conclusion, the experimental outcomes unequivocally underscore the significant application potential of these Tb3+-doped GCs in the territory of warm WLED lighting.

Bifunctional Ligand Passivation Enables Stable Blue Mixed-Halide CsPb(Br/Cl)3 Perovskite Quantum Dots toward Light-Emitting Diodes.

Mixed-halide CsPb(Br/Cl)3 perovskite quantum dots (PeQDs) have attracted extensive attention in light-emitting diodes (LEDs), but their low photoluminescent efficiency and especially poor stability impede their practical applications. Here, we employ bifunctional didodecyldimethylammonium thiocyanide (DDASCN) with a pseudohalogen SCN- and branched DDA+ to obtain blue-emitting CsPbBr2Cl PeQDs. DDASCN significantly boosts the photoluminescence quantum yield to 92% by inhibiting nonradiative recombination. Importantly, DDASCN PeQDs show excellent stabilities against air, UV light, heat, and polar solvents. These improved performances were explained by density functional theory calculation, which shows that SCN- fills the Cl- vacancy by simultaneously binding with undercoordinated Pb2+ and Cs+, while DDA+ connects undercoordinated Br- and lies parallel to the PeQD core, leading to efficient passivation and a strong binding capacity. Finally, we achieved high-performance white LEDs by integrating our PeQDs, resulting in a color-rendering index of 92.9, a color gamut of 119.61%, and chromaticity coordinates of (0.33, 0.33). This provides an effective method to obtain efficient and stable CsPb(Br/Cl)3 PeQDs for practical applications.

Upconversion and Downshifting Luminescence from KSrVO4:Er3+ Nanophosphor with Judd-Ofelt Parameters.

This study investigates the synthesis and characterization of KSrVO4 phosphors doped with Er3+ ions using combustion synthesis route by using urea as a fuel. X-ray diffraction analysis confirmed the orthorhombic phase and nano-scale crystallite size of around 21nm, while transmission electron microscopy showed spherical and rod-shaped morphologies. The studies detected upconversion emission spectra at 526, 542 and 643nm, representing green and red transitions under 980nm excitation. Downshifting emissions under 350nm excitation revealed peaks at 492, 544 and 680nm. The critical quenching concentration was 2.5mol%, resulting from dipole-quadrupole interactions among dopant ions. The direct and indirect optical band gaps were calculated as 3.61 and 3.41eV, respectively. The calculated chromaticity coordinates and color correlated temperature values of the phosphor surpassed 5000K, suggesting its viability for cool LED applications. These findings emphasize KSrVO4:Er3+ as a promising greenish component in white LEDs and a potent upconverting luminescence material for bio-imaging and photovoltaics.

A Novel Synthesis Method of Dumbbell-like (Gd1-xTbx)2O(CO3)2·H2O Phosphor for Latent Fingerprint.

A novel method for synthesizing dumbbell-shaped (Gd1-xTbx)2O(CO3)2·H2O (GOC:xTb3+) phosphors using sodium carbonate was investigated. An amount of 1 mmol of stable fluorescent powder can be widely prepared using 3-11 mmol of Na2CO3 at a pH value of 8.5-10.5 in the reaction solution. The optimal reaction conditions for the phosphors were determined to be 7 mmol for the amount of sodium carbonate and a pH of 9.5 in the solution. Mapping analysis of the elements confirmed uniform distribution of Gd3+ and Tb3+ elements in GOC:xTb3+. The analysis of fluorescence intensity shows that an optimal excitation wavelength of 273 nm is observed when the concentration of Tb3+ is between 0.005 and 0.3. The highest emission intensity was observed for GOC:0.05Tb3+ with a 57.5% maximum quantum efficiency. The chromaticity coordinates show that the color of GOC:Tb3+ is stable and suitable for fluorescence recognition. Latent fingerprint visualization reveals distinctive features like whorls, hooks, and bifurcations. Therefore, the sodium carbonate method offers an effective alternative to traditional urea chemical reaction conditions for preparing GOC:Tb3+.

Synthesis and color-tunable emission of ZnGaOx with different cation ratios by a polyacrylamide gel method

ZnGaOx nanoparticles with varied ratios of Zn2+ to Ga3+ were synthesized by a polyacrylamide gel route. The phase purity and structure are confirmed by X-ray diffraction (XRD), Fourier transform infrared spectrometer (FTIR) and X-ray photoelectron spectrometer (XPS). High crystal quality and elemental distribution are determined by transmission electron microscopy (TEM) measurements. The band gaps of the samples ranging from 3.22 to 4.47 eV are estimated by ultraviolet–visible (UV–Vis) diffuse refectance spectroscopy (DRS). Under the excitation of 325 nm laser light, ZnGaOx nanoparticles with the Zn2+/Ga3+ molar ratios of 0.8:2 and 0.7:2 show two emission peaks at 415 and 510 nm. A marked emission band at 695 nm is observed from the samples with Zn2+/Ga3+ molar ratios of 0.6:2, 0.5:2 and 0.4:2. The luminescence mechanism is discussed based on the experimental results. The luminescence color of as-synthesized samples gradually shifts from blue-green to green-yellow region with decreasing Zn2+/Ga3+ ratio. Interestingly, the sample with Zn2+/Ga3+ ratio of 0.7:2 has the CIE chromaticity coordinates of (x = 0.26, y = 0.33) close to the coordinates (x = 0.33, y = 0.33) of pure white light. Together, ZnGaOx phosphors with different emission colors without doping with rare earths have considerable potential applications in tunable light emitting diodes (LEDs) and color display.

A novel framework of smart monitoring to face the challenges of tree management in historic gardens

Historic gardens are green spaces characterised by tree stands with several veteran specimens of high artistic and cultural value. Such valuable plant components have to cope with biotic and abiotic stress factors as well as ongoing senescence processes. Maintaining tree health is therefore crucial to preserve their ecosystem services, but also to protect the monument and visitor health. In this context, finding smart, fast and cost-effective management solutions to monitor health and detect critical conditions for both stands and individual veteran trees can promote garden conservation. For this reason, we developed a novel framework based on Sentinel2 imagery, LiDAR sources and automatic cameras to identify risk spots regarding trees in historic gardens. The pilot study area consists of two closed Italian gardens from the 16th century, which were analysed as a unique Historic Garden System (HGS). The tree health status at stand level was assessed using a criterion based on the Normalized Difference Vegetation Index weighed on tree volume (NDVIt) and validated by a visual crown defoliation assessment. At the tree level, the health status of four veteran trees defined by the NDVIt was also evaluated using green chromatic coordinates (GCC) obtained from digital images acquired by cameras at daily intervals during one growing season. The 33% of the tree population was classified as being in poor health, i.e. “at risk”. Veteran trees classified as “at risk” showed an anticipation of phenological phases and a lower GCC compared to reference trees. Despite variability determined by Sentinel medium resolution, the proposed framework showed good accuracy (0.74) for monitoring historical gardens. The semi-automatic risk point mapping system tested here proved to be effective in facilitating the management of historic gardens, which in turn could be applied in the wider context of urban greening.

Dazzling red-emitting Ca2EuMO6 (M = Sb, Nb, Ta) double-perovskite phosphors with potential application in phosphor-converted white light-emitting diodes

In this paper, three new efficient Eu3+-activated Ca2EuMO6 (M = Sb, Nb, and Ta) red-emitting phosphors with outstanding luminescence properties were prepared by using the high-temperature solid-state reaction method. X-ray diffraction and Rietveld refinements revealed the double-perovskite structure of Ca2EuMO6 (M = Sb, Nb, and Ta) compounds. Photoluminescent excitation and emission spectra, decay lifetimes, CIE chromaticity coordinates, color purity values, internal quantum efficiency, and thermal stability were discussed in detail. Under the excitation of 395 nm near-ultraviolet light, these Ca2EuMO6 (M = Sb, Nb, and Ta) phosphors demonstrated bright narrow-band red emissions with peaks at 592, 620, 656, and 703 nm due to the 5D0→7FJ (J = 1–4) transitions of Eu3+ ions. The internal quantum efficiencies of the Ca2EuSbO6, Ca2EuNbO6, and Ca2EuTaO6 samples were determined to be 39.3%, 41.6%, and 40.4%, respectively. Impressively, the emission intensity of Ca2EuNbO6 is about 1.25 times higher than that of commercial Y2O3:Eu3+ red phosphor. CIE color coordinates of Ca2EuMO6 (M = Sb, Nb, and Ta) phosphors were calculated to be (0.6748, 0.3250), (0.6800, 0.3198), and (0.6790, 0.3208), respectively; along with high color purity of 90.7%, 93.2%, and 92.7%. Besides, their thermal stability was also investigated, and the corresponding emission intensities of Ca2EuMO6 (M = Sb, Nb, and Ta) at 423 K were respectively maintained at 73%, 86%, and 80% of that at 303 K. All results show that these newly developed red-emitting Ca2EuMO6 (M = Sb, Nb, and Ta) phosphors possess potential applications in white light-emitting diodes.

Garnet-type cyan-green-emitting SrLu2Ga1.5Al2.5SiO12:Ce3+ phosphor with high quantum efficiency, thermal stability, and water resistance for blue-excited WLEDs

Nowadays, high-quality phosphor-converted white light-emitting diodes (pc-WLEDs) ought to include cyan-emitting phosphors allowing for full-spectrum light similar to sunlight. Herein, we report a garnet-structured Ce3+-doped SrLu2Ga1.5Al2.5SiO12 (SLGASO) phosphor that significantly compensates for the absence of cyan light, known as the “cyan cavity”. The SLGASO host crystallizes into a cubic structure with the space group. The cell parameters were determined using Rietveld refinement. Under 430 nm blue excitation, SLGASO:Ce3+ emits intense cyan-green light in the 450‒700 nm wavelength range. The representative SLGASO:0.07Ce3+ phosphor has an internal quantum efficiency (IQE) of 95.4% and excellent thermal stability, remaining 92.7% of its initial emission intensity at 152 °C. After 155 d of immersion in water, the luminous intensity of SLGASO:0.07Ce3+ remains constant, confirming its waterproofness. Furthermore, a pc-WLED device with luminous efficiency (LE) of 101.58 lm/W, color rendering index (Ra) of 91, correlated color temperature (CCT) of 4536 K, and Commission Internationale de L’Eclairage (CIE) chromaticity coordinates of (0.3555, 0.3390) was fabricated by combining as-prepared cyan-green-emitting SLGASO:0.07Ce3+, yellow-emitting Y3Al5O12:Ce3+ (YAG:Ce3+), and red-emitting (Ca,Sr)AlSiN3:Eu2+ phosphors, as well as a 450 nm blue chip. These findings indicate that SLGASO:0.07Ce3+ phosphor can bridge the cyan gap and improve the performance of as-fabricated full-visible-spectrum WLEDs.