White Regions Research Articles

Research on multicolor luminescence, structural and energy transfer in Dy/Eu co-doped fluoroborate glasses for W-LEDs

The composition of 50B2O3-20Al2O3-5Na2O-10Bi2O3-15CaF2-xDy-yEu (x = 0.1，0.5，1.0，1.5，2.0，3.0 mol%; y = 0, 0.1, 0.3, 0.5, 0.7, 1.0 mol%) (BACDE) glass were prepared using the traditional melt quenching process. The structure of the BACDE glass was analyzed using XRD analysis and Fourier infrared spectroscopy. The photoluminescence spectra show that concentration quenching occurs when Dy concentration is higher than 1.0mol% in fluoroborate glass. By varying the excitation circumstances and obtaining emission spectra at three distinct excitation wavelengths (364, 382, and 395 nm), the luminescence characteristics of BACDE glass were examined. The results indicate that when excited at 364 nm, the luminescence of the BACDE glass is close to the white region, a controlled color shift is achieved within a certain range. The spectral superposition and fluorescence attenuation spectra of Dy3+ emission and Eu3+ absorption demonstrate the energy transfer from Dy3+ to Eu3+, and the main transfer mechanism is the electric dipole-electric dipole interaction. The most optimal chromaticity coordinates for the BACDE glass samples were (0.3832,0.3858), (0.3672,0.3949), with a color temperature (CCT) of approximately 3992K at 364 nm excitation. By controlling the Dy/Eu content, BACDE glass can exhibit warm white, and light reddish-orange glow. Thus, Eu3+/Dy3+ co-doped BACDE glasses have potential applications in white luminescent materials and dimmable materials.

Dy3+ ions in fluorophosphate glasses for luminescent white light applications

Abstract In this study, a series of fluorophosphate (FP) glasses, activated with Dy3+ ions and displaying concentration dependence, have been prepared and analysed for their suitability in luminescent white light applications. The melt quenching method was utilized to fabricate a set of FP glasses, doped with Dy3+ ions and possessing the composition of (60 − x) P2O5 + 10MgO + 10ZnO + 10BiF3 + 10KF + xDy2O3, where x ranges from 0.1 to 2.0 mol%. The structural properties of the samples were analysed using x-ray diffraction (XRD), scanning electron microscope (SEM), Fourier transform infrared (FTIR), and Raman spectroscopy while the optical properties of the samples were studied using absorption and emission spectra. The amorphous nature of the FP glasses was confirmed through SEM analysis and XRD profiles. Moreover, the presence of elements in their composition was verified using EDX. The FTIR spectra of the FP glasses exhibited vibration bands consistent with the characteristic phosphate groups, which was further supported by Raman analysis. The absorption spectra were used to calculate oscillator strengths (f exp & f cal) and Judd–Ofelt (JO) parameters Ω λ (λ = 2, 4, 6). The values of Ω λ (λ = 2, 4, 6) followed this order: Ω6 > Ω2 > Ω4. The emission spectra displayed three prominent transitions in the UV–visible region: (4F9/2 → 6H15/2) blue, (4F9/2 → 6H13/2) yellow, and (4F9/2 → 6H11/2) red. The peak at 553 nm (4F9/2 → 6H13/2) was the most intense and dominant. Radiative characteristics were evaluated from the emission spectra through the employment of JO intensity parameters and refractive indices. The Y/B intensity ratio values were greater than 1, indicating the high covalency of Dy3+ ions. The colour coordinates (x, y) and correlated colour temperature values of CIE 1931 were situated in the cool white region. The comprehensive analysis suggests that these glasses have the potential to become highly favourable candidates as luminescent components for solid-state white light emitting instruments.

Cerium-infused tungstate nanocrystals: Illuminating the future of solid-state lighting

Rare earth based luminescent materials have emerged as a focal point of the scientific investigation owing to their remarkable optical behaviour and potential applications. An effort has been made to develop a series of Ce3+ doped CaWO4 nano-phosphors using an ethylene-glycol assisted reflux route. The detailed structural and morphological properties have been examined through various analytical techniques. The +3-oxidation state of the activator ion Ce has been verified through the XPS study. The change in optical band gap due to the substitution is well discussed using diffuse reflectance spectroscopy. In Photoluminescence study, a broad emission centred at 465 nm is observed due to the 5D3/2→2FJ transitions (J = 7/2 and 5/2) and a significant enhancement in the emission peak is obtained for the optimized phosphor. Concentration quenching phenomenon, observed after 3 mol% of Ce3+ is mainly mediated by the electric multipole-multipole type interaction. The CIE diagram indicates the tuning of emission colour from blue to white region and the emission near white region for the optimized phosphor is further authenticated by its low colour purity value (43 %). The effective tunability of photo-physical properties and colorimetric parameters suggest the applicability of the optimized nano-phosphor in solid state lighting especially for outdoor illumination.

Russulaceae of the Pakaraima Mountains of Guyana 5. Two newly described diminutive species in a novel lineage of the crown clade of Russula (Russulaceae)

Much of our previous work documenting fungal biodiversity in Guyana has been centered in forests of Dicymbe corymbosa Spruce ex Benth., which forms monodominant stands in the white sands region of Guyana. In order to begin to assess fungal biodiversity associated with other ectomycorrhizal host trees found in Guyana, expeditions were conducted to areas containing Dicymbe altsonii and Pakaraimaea dipterocarpacea. In this paper, we describe two new species of Russula from Guyana with diminutive basidiomata: R. lilliputia and R. pakaraimaeae, found in association with these tree hosts, using a combined approach of morphological characterization and molecular analyses. Together with R. gelatinivelata, which we previously described from Guyana, R. lilliputia and R. pakaraimaeae form what appears to be a new lineage within the crown clade of Russula, sister to the subsect. Auratinae. Synapomorphies for the lineage include a pruinose to subtomentose pileus in dry conditions, suprapellis comprised of inflated cells that give rise to long cylindrical or digitate, and sinuous, thin or thick-walled pileocystidia that are strongly emergent, easily disarticulate in microscopic preparations, and have contents that are acid resistant in Basic Fuchsin, pruinose to subomentose patches on the stipe, suprahilar plage on the basidiospores, spore ornamentation of mostly isolated verrucae, and geographic distribution restricted to the Pakaraima Mountains of Guyana. Full descriptions, photos, line drawings of microscopic features, and comparisons with related species are provided.

Combustion synthesis and photoluminescence of Ca2SrWO6:Dy3+ double perovskite: An approach for white light emission

Luminescent Ca2SrWO6:Dy3+ double perovskites are synthesized via the combustion route of material synthesis, wherein urea is taken as fuel. The as-prepared phosphor series comprehensively characterized for their structural and photoluminescence (PL) properties. The Rietveld refinement of XRD data revealed monoclinic crystallized microcrystals with mixed particles of the size of less than 1 µm, studied via SEM. Ca2SrWO6:Dy3+ displayed standard Dy3+ transitions 4F9/2–6H15/2 (blue emission) and 4F9/2–6H13/2 (yellow emission) collectively resulted in white light emission, confirmed via CIE study. Under 278 and 388 excitations, 2 mol% doping of Dy3+ found to be optimum concentration, beyond which concentration quenching is observed due to dipole–dipole interaction. The Y/B ratio ∼1 shows potential to produce white light and make phosphor suitable for WLED applications. The Ca2SrWO6:Dy3+ phosphor displayed notably high thermal stability with PL intensity persisted 77.6 % at LED burning temperature (150 °C) when compared to PL intensity attained at room-temperature, which is basically due to the rigid perovskite structure. In addition, the PL decay lifetime of 4F9/2 state was calculated by utilizing decay curves. Subsequently, the PL quantum efficiency and non-radiative relaxation rate are determined. The theoretical model of Auzel’s fit function is used to calculate to quantum efficiency and was found to be 93.27 % for Ca2SrWO6:2 % Dy3+ phosphor. Moreover, the photometric results reveals that the CIE points are lies in white region of CIE diagram with comparable CCT. The collective results indicated the utility of the phosphor for potential WLED applications.

Copper(II), zinc(II) and cadmium(II) complexes with the O-picolyl ether of chiral α-aminooxime of natural (+)-limonene: synthesis, structures, luminescence and cytotoxicity

Copper(II), zinc(II) and cadmium(II) complexes, [CuLCl2], [ZnLCl2] and [CdLCl2], with a new derivative of chiral α-aminooxime of natural (+)-limonene bearing a pycolyl group (L) were synthesized. The complexes are mononuclear, the L molecules act as N,N,N-tridentate chelating ligands. The computations support the fact that the N,N,N–chelation by a metal ion is thermodynamically preferred over the N,N–chelation for all complexes. The ligand L and the complexes [ZnLCl2] and [CdLCl2] exhibit fluorescence, with the emission spectra depending on the excitation wavelength. L emits in close to white region, while the Zn(II) and Cd(II) complexes demonstrate blue emission. Due to chelation-induced fluorescence enhancement effect, the fluorescence quantum yield increases when going from L to [ZnLCl2] and [CdLCl2]. The complex [CdLCl2] displays cytotoxicity against the HepG2 cell line (IC50 = 14.3 ± 1.5 μM), which is almost twice as high as that of cisplatin. The human breast adenocarcinoma cell line (MCF-7) is more sensitive to [CuLCl2] (IC50 = 43.4 ± 0.4 μM) than to [CdLCl2].

Synthesis and tunable luminescence properties of SrY₂O₄:Dy³⁺ phosphors

In this study, SrY₂O₄:Dy³⁺ phosphors were synthesized using the solid-state reaction method and evaluated after heat treatment at 1300 °C for 5 h. XRD analysis confirmed the orthorhombic structure of SrY₂O₄ with residual Y₂O₃ present. The addition of Dy³⁺ ions caused lattice expansion, impacting grain size and crystallinity. SEM images showed that the phosphor particles had irregular shapes with minimal size variation, although they tended to agglomerate due to high-temperature heat treatment. Optical analysis revealed significant absorption and emission peaks, with a strong excitation band in the 200–306 nm range and prominent sharp peaks in the 306–480 nm range, particularly at a 0.5 mol% doping concentration. Emission spectra indicated the highest intensity at 0.5 mol% Dy³⁺ concentration, with intensity decreasing due to concentration quenching at higher levels. Thermal stability tests showed peak emission intensity at 70 °C, with stability maintained up to 190 °C before notable thermal quenching. Chromaticity coordinates remained within the warm white region at both temperatures. This study provides detailed insights into the effects of Dy³⁺ doping on the structural, optical, and thermal properties of SrY₂O₄ phosphors. Compared to previous studies on rare-earth-doped SrY₂O₄ phosphors, this work is the first to systematically explore the substitution of Y³⁺ ions with Dy³⁺ ions until full replacement. The study not only confirmed that the highest emission intensity occurs at 0.5 mol% Dy³⁺ concentration, but also demonstrated that Dy³⁺-doped SrY₂O₄ phosphors exhibit excellent thermal stability, with emission stability maintained below 150 °C. These findings expand the potential applications of Dy³⁺-doped SrY₂O₄ phosphors, particularly in high-temperature environments and solid-state lighting.

Dysprosium ion concentration variations and their comprehensive influence on the physical, structural and optical properties of multi-component borate glasses for luminescence tailoring

A set of Zinc Strontium Lithium Fluoroborate (ZSLFB) glasses with different concentrations of Dysprosium ions (Dy3+) was created using the melt quench technique. The presence of non-crystallinity and various functional groups have been confirmed via X-Ray Diffraction (XRD) and Infrared Fourier Transform FT-IR measurements, respectively. The band gap values obtained from Tauc plot were utilised to analyse the optical characteristics. The photoluminescence (PL) emission spectra display three well-defined intensity peaks at wavelengths of 481, 574, and 664 nm. The intensity of peaks exhibits an ascending trend until a concentration of 0.5 mol% of Dy3+ ions is reached, after which it decreases. The PL intensity maintains up to 82 % at 200° C to room temperature, showing excellent thermal stability. The Judd Ofelt (J-O) parameter values pursue the Ω2 > Ω6 > Ω4 pattern, which shows its asymptotic nature. The CIE coordinates were assessed and determined to fall inside the white region. The interaction in the non-radiative energy transfer process was elucidated by utilizing the Dexter theory and Inokuti-Hiryama (I-H) model.

Marine Hunting of Pinnipeds (Pinnipedia) on the Coats of the White Sea in the Eneolithic

This is a study of initial stages of adaptation of the ancient human population to the use of aquatic food supplies in the White Sea. The main aim of archaeozoological analysis was to study the processes of formation of faunal remains and strategies on seals hunting during the Eneolithic in the White Sea region. The archaeological source material consists of faunal remains recovered from two Eneolithic sites of the Kandalaksha bay. The results of archaeozoological studies confirmed the high importance of the ringed seal and harp seal in the hunting prey of the inhabitants of the studied sites. Eneolithic hunting strategies of the White Sea region were closely related to the behavioral and ecological patterns of seals. The seal hunt was based on a model of exploiting a massive seasonal resource. Hunting pressure on the ringed seal and harp seal populations was significant. Seals were the main suppliers of meat, skin and fat for the inhabitants of the Eneolithic sites of this part of Fennoscandia. The studies of the lithic tools from the Early Metal period settlements from Kandalaksha bay provide additional evidences of a specialized marine hunting. Apparently, in the Eneolithic (IV – III millennia calBC), the economic and cultural type of sea hunters was formed on the shores of the White Sea.

Preparation and properties of GdPO4:Dy3+ phosphors and ceramics with high thermal stability

In this work, Gd1-xPO4:xDy3+ powders were synthesized by calcining the mixed raw materials at 1273 K and the optimal doping concentration was determined. Then the optimized composition powders were fabricated as ceramics after granulation, pressing and sintering. Meanwhile, the luminescent properties of the phosphors and ceramics, especially the thermal stability, were discussed. The results revealed that Gd1-xPO4:xDy3+ exhibited two strong emission peaks of blue light and yellow light under the excitation of 349 nm, ascribed to the energy level transition from 4F9/2 to 6H15/2 and 6H13/2 of the electrons of Dy3+, and the color coordinates were located in the white light region. The optimal doping concentration of Dy3+ was found as 0.1, and the electronic dipole-dipole interaction contributed to the concentration quenching. It was noted that the phosphors had good thermal stability. Specifically, the thermal stability was further improved after the ceramics was formed and the relative intensity between the blue and yellow changed the opposite, indicating different occupation sites of Dy3+.

Diabetic Mice Spleen Vulnerability Contributes to Decreased Persistence of Antibody Production after SARS-CoV-2 Vaccine.

During the COVID-19 pandemic, diabetic and obese patients experienced higher rates of hospital admissions, severe illness, and mortality. However, vaccinations failed to provide those vulnerable populations the same level of protection against COVID-19 severity as those without diabetic and obese phenotypes. Our study aimed to investigate how diabetes mellitus (DM) impacts the immune response following vaccination including the artificially designed trimeric SARS-CoV-2 spike (S)-protein. By using two diabetic mouse models, ob/ob mice (obese, hyperglycemic, and insulin-resistant) and STZ-treated mice (insulin-deficient and hyperglycemic), we observed a significant reduction in S-protein-specific IgG antibody titer post-vaccination in both diabetic models compared to wild-type (WT) mice. Both diabetic mouse models exhibited significant abnormalities in spleen tissue, including marked reductions in splenic weight and the size of the white pulp regions. Furthermore, the splenic T-cell and B-cell zones were notably diminished, suggesting an underlying immune dysfunction that could contribute to impaired antibody production. Notably, vaccination with the S-protein, when paired with an optimal adjuvant, did not exacerbate diabetic cardiomyopathy, blood glucose levels, or liver function, providing reassurance about the vaccine's safety. These findings offer valuable insights into potential mechanisms responsible for the decreased persistence of antibody production in diabetic patients.

Novel Tm3+/Dy3+ co-doped CaMoO4 transparent glass-ceramic phosphor for white LED applications

To develop new inorganic luminescent materials, a set of Dy3+/Tm3+ co-doped molybdate precursor glasses (PGs) were manufactured using the conventional melting method, and a novel CaMoO4 transparent fluorescent glass-ceramic (GC700-2 h) was achieved via controlled crystallization of PG at 700 ℃ for 2 h. The luminescent color of the glass phosphor was facilely modulated by varying the doping levels of Dy3+ and Tm3+. The glass phosphor with optimal doping concentration of 0.6Dy3+ and 0.6Tm3+ exhibits a color coordinate of (0.3334, 0.3107). Compared with PG, the luminous intensity and quantum yield of GC700-2 h sample is obviously increased, and GC720-2 h sample displays the color coordinate (0.3292, 0.2852), belonging to the standard white light region. Moreover, GC720-2 h sample possesses good thermal stability in fluorescence property. The white LED lamp encapsulated with GC720-2 h exhibits color temperature of 7564 K and color rendering index of 75.3. These results clearly show that the 0.6Dy3+/0.6Tm3+ co-doped glass and CaMoO4 glass-ceramic could be used as potential candidate material in the field of white light-emitting diodes.

Harnessing the inherent photoluminescence of Ba2MgTeO6 double perovskite phosphor for visible to near infrared pc-LED applications

Phosphor-converted LEDs (pc-LEDs) emitting in the visible region based on undoped tellurate double perovskites have not been explored till now. A cyan-emitting pc-LED is fabricated using the host Ba2MgTeO6 double perovskite for the first time. The as-fabricated cyan LED emits light in the visible region with the maximum emission at 484 nm. The obtained CIE coordinates of (0.26, 0.37) ensure a cyan light, and LED exhibits superior color stability even at higher input drive current. An attempt to develop a white emitting phosphor was done by substituting Eu3+ ions into the Ba2MgTeO6 matrix. Followed by this, a phosphor converted LED emitting in the bluish white region was fabricated by combining near UV chip and BMTO: 0.02 Eu3+ phosphor. Further, an inherent near-infrared (NIR) luminescence in Ba2MgTeO6 is also discovered and it originates from the 3T1u, 3A1u – 1A1g electronic transitions within the Te4+ ions. Upon 367 nm excitation, Ba2MgTeO6 exhibits strong broadband NIR emission, which spans from 780 nm to 1150 nm with a maximum emission at 889 nm and full width at half maximum (FWHM) of about 115 nm. Finally, an efficient pc-LED emitting in the NIR region is fabricated using the intrinsic near-infrared luminescence observed in the Ba2MgTeO6 phosphor. The pc-LED covering the near infrared region can be potentially used for various applications, including plant cultivation, biosensors, night vision cameras, etc.

Investigation of structural, optical characteristics of Gd3+ doped phosphate glass for radiation shielding applications

Gadolinium doped phosphate glass was created with a composition of 70 P2O5 + 5Al2O3 + 5 Ba2CO3 + 9 KF2 + 5 MnO2 + 5 SnO+1 Gd2O3 by using the melt-quenching process. The prepared glass sample’s amorphous nature was confirmed by the X-ray diffraction analysis. FT-IR examination confirms the presence of phosphate functional groups. Glass’s optical band gap was found to be 3.5 eV using Tauc’s plot method. The photoluminescence analysis indicates that the emission band at around 311 nm. The Commission International de I’Eclairage (CIE) was employed. It was identified that the computed chromaticity coordinate values (x = 0.3164 and y = 0.3371) were situated in the summer sunlight zone, close to the white light region. The attenuation capabilities of the gadolinium-doped phosphate glass sample were validated by the gamma ray shielding parameters. The mass attenuation coefficient and Mean free path of the prepared glass were fund to be 4.41 × 105 cm2/g at 0.015 MeV and 12.4 cm at 15 MeV respectively. In terms of infiltration deepness up to 40 MFP, the energy-related energy buildup factor (EBF) and energy absorption buildup factor (EABF) of glasses were calculated using the five (a, b, c, d, and Xk) parameters of the G-P fitting scheme. All of the results show that the synthetic glass can be used as shielding materials against gamma radiation.

A Diffusion Tensor Imaging White Matter Atlas of the Domestic Canine Brain

Abstract There is increasing reliance on magnetic resonance imaging (MRI) techniques in both research and clinical settings. However, few standardized methods exist to permit comparative studies of brain pathology and function. To help facilitate these studies, we have created a detailed, MRI-based white matter atlas of the canine brain using diffusion tensor imaging. This technique, which relies on the movement properties of water, permits the creation of a three-dimensional diffusivity map of white matter brain regions that can be used to predict major axonal tracts. To generate an atlas of white matter tracts, thirty neurologically and clinically normal dogs underwent MRI imaging under anesthesia. High-resolution, three-dimensional T1-weighted sequences were collected and averaged to create a population average template. Diffusion weighted imaging sequences were collected and used to generate diffusivity maps, which were then registered to the T1-weighted template. Using these diffusivity maps, individual white matter tracts—including association, projection, commissural, brainstem, olfactory and cerebellar tracts—were identified with reference to previous canine brain atlas sources. To enable the use of this atlas, we created downloadable overlay files for each white matter tract identified using manual segmentation software. In addition, using diffusion tensor imaging tractography, we created tract files to delineate major projection pathways. This comprehensive white matter atlas serves as a standard reference to aid in the interpretation of quantitative changes in brain structure and function in clinical and research settings.

Florbetaben amyloid PET acquisition time: Influence on Centiloids and interpretation.

Amyloid positron emission tomography (PET) acquisition timing impacts quantification. In florbetaben (FBB) PET scans of 245 adults with and without cognitive impairment, we investigated the impact of post-injection acquisition time on Centiloids (CLs) across five reference regions. CL equations for FBB were derived using standard methods, using FBB data collected between 90 and 110 min with paired Pittsburgh compound B data. Linear mixed models and t-tests evaluated the impact of acquisition time on CL increases. CL values increased significantly over the scan using the whole cerebellum, cerebellar gray matter, and brainstem as reference regions, particularly in amyloid-positive individuals. In contrast, CLs based on white matter-containing reference regions decreased across the scan. The quantification of CLs in FBB PET imaging is influenced by both the overall scan acquisition time and the choice of reference region. Standardized acquisition protocols or the application of acquisition time-specific CL equations should be implemented in clinical protocols. Acquisition timing affects florbetaben positron emission tomography (PET) scan quantification, especially in amyloid-positive participants. The impact of acquisition timing on quantification varies across common reference regions. Consistent acquisitions and/or appropriate post-injection adjustments are needed to ensure comparability of PET data.

Fluorescent Aromatic Polyether Sulfones: Processable, Scalable, Efficient, and Stable Polymer Emitters and Their Single-Layer Polymer Light-Emitting Diodes.

In this study, fully aromatic polyether sulfones were developed, bearing blue, yellow, and orange-red π-conjugated semiconducting units. Carbazole-, anthracene-, and benzothiadiazole-based fluorophores are copolymerized with a diphenylsulfone moiety. A diphenylpyridine comonomer was additionally utilized, acting as both a solubilizing unit and a weak blue fluorescent group. Using this rationale, fluorescent polyarylethers with high molecular weights, up to 70 kDa, were developed, showing film formation ability and high thermal stability, while preserving excellent solubility in common organic, nonvolatile, and nonchlorinated solvents. Fine-tuning of the emission color was achieved through subtle changes of the comonomers' type and ratio. Single-chromophore-bearing copolymers emitted in the blue or the yellow region of the visible spectrum, while the dual-chromophore-bearing terpolymers emitted throughout the visible spectrum, resulting in white light emission. Solutions of 20 wt% in polar aprotic solvents at ambient conditions allowed the deposition of fluorescent copolyethers and printing from non-chlorinated solvents. All polyethers were evaluated for their structural and optoelectronic properties, and selected copolymers were successfully used in the emitting layer (EML) of organic light-emitting diode (OLED) devices, using either rigid or flexible substrates. Remarkable color stability was displayed in all cases for up to 15 V of bias voltage. The Commission Internationale de L'Eclairage (CIE) of the fabricated devices is located in the blue (0.16, 0.16), yellow (0.44, 0.50), or white region of the visible spectrum (0.33, 0.38) with minimal changes according to the ratio of the comonomers. The versatile methodology toward semiconducting polyethersulfones for polymer light-emitting diodes (PLEDs) developed herein led to the scaled-up production of luminescent polymers of up to 25 g of high-molecular-weight single batches, demonstrating the effectiveness of this approach as a straightforward tool to facilitate the synthesis of flexible and printable EMLs for large-area PLED coverage.

Investigation on Luminescence Properties of Dy3+ Ions Doped NaBaB9O15 Phosphors for Optoelectronic Applications.

A series of Dy3+ ions doped NaBaB9O15 phosphors with different dopant concentration was synthesized by solid state reaction. The phase purity was checked by X-ray diffraction analysis and the functional groups present in as prepared phosphors was investigated with the help of FTIR spectral analysis. Under 386nm excitation, the photoluminescence spectra exhibit three emission bands around 482nm, 574nm and 664nm due to 4F9/2→6HJ/2 (J = 15, 13, 11) transions respectively. The optimum doping concentration of Dy3+ ions was found to be 5mol%. The color coordinates are estimated from the emission spectra to check the dominant emission color and the color coordinates of the studied phosphors are fall on white region of CIE 1931 diagram. The decay curve analysis was made to determine the lifetime of excited state of Dy3+ ions and the decay curves are exhibited bi-exponential behavior irrespective of Dy3+ ion concentration. All these measurents are done in room temperature and the results obtained from these studies are discussed in detail to claim their usage in light emitting devices.

Structural characterization and luminescence characteristics of Dy3+ doped Sr9Y2W4O24 phosphor for application in white-LEDs

In this research, a series of Dy3+ ions doped Sr9Y2W4O24 (SYWO) phosphors was prepared for the application in white-LEDs and display devices. The structure, surface, and photo-luminescent (PL) behaviour of the samples were studied. X-ray diffraction (XRD) and Fourier Transform Infra-Red (FT-IR) spectroscopy indicated the formation of single phase particles with no contaminants with various vibrational bands present in the host lattice. The synthesised powders showed agglomeration with the average crystallite size to be in the range of 22–27 nm. The optical band gaps were estimated using diffuse reflectance spectral (DRS) data. The emission spectra of SYWO: xDy3+ (1.0, 2.0, 3.0, 4.0, & 5.0 mol%) have been obtained at different excitation wavelengths of 354, 367, and 391 nm. The SYWO phosphors emit intense blue and yellow colors at 491 nm (4F9/2 → 6H15/2), 576 nm (4F9/2 → 6H13/2) & 679 nm (4F9/2 → 6H11/2), respectively. Furthermore, from the CIE 1931 diagram, it is evident that the emission from these Dy3+ doped phosphors lies in the white region. The lifetime of excited Dy3+ ions decreased with increasing Dy3+ concentration as seen in the luminescence decay graphs. Finally, to determine the phosphor's luminescence thermal stability, temperature dependent photoluminescence (TD-PL) was recorded and the activation energy calculated from this study was found to be 0.231 eV. In the light of aforementioned results, we can conclude that Dy3+ doped Sr9Y2W4O24 phosphors could be used in construction of w-LEDs or as white-emitting luminescent materials in various photonic devices and other photonic applications.

Effect of Cooling Method on Microstructure and Microhardness of CuCrFeMnNi High-Entropy Alloy

This study investigated four cooling methods for CuCrFeMnNi high-entropy alloy, namely, furnace cooling, air cooling, oil cooling, and water cooling (designated as FC, AC, OC, and WC, respectively), following a 12 h treatment at 800 °C. Results indicate that all four cooled alloys consisted of two FCC solid-solution phases (FCC1 and FCC2) and ρ phases. However, the FC alloy primarily contained FCC2 as the main phase and FCC1 as the secondary phase. The other three cooling methods yielded alloys with FCC2 as the primary phase and FCC1 as the secondary phase. With an increase in cooling rate, the content of the FCC1 phase gradually increased, that of the ρ phase initially decreased and then increased, and that of the FCC2 phase gradually decreased. The microstructure of the CuCrFeMnNi high-entropy alloy under the four cooling methods consisted of gray-black dendrites rich in Cr-Fe and white dendrites rich in Cu. Black ρ-phase particles predominated the dendrite region. As the cooling rate increased, the white interdendritic regions shrank, and the gray-black interdendritic regions expanded. The FC alloy exhibited the lowest microhardness at approximately 202.6 HV. As the cooling rate increased, the microhardness of the alloy progressively increased. The microhardness of the WC alloy was the highest, at approximately 355 HV. The strengthening mechanisms for all the alloys were primarily solid-solution strengthening and second-phase precipitation strengthening.