Search Results (362)

Mn⁴⁺-doped fluoride red phosphors are widely used in white LED lighting and display applications due to their excellent luminescent properties. However, their synthesis relies heavily on highly toxic aqueous hydrofluoric acid, which not only causes severe environmental and soil/water pollution but also makes it difficult to control the microstructure of the products due to the rapid reaction rate. In this study, low-melting-point NH₄HF₂ was used as the molten salt, with KMnO₄ and MnF₂ as manganese sources, to synthesize the red phosphor K₃AlF₆: Mn⁴⁺ via the molten salt method. After the reaction, impurities such as NH₄HF₂ were removed by washing with a dilute H₂O₂ solution. The microstructure, photoluminescence properties, thermal quenching behavior, and application in warm white light-emitting diodes (W-LEDs) of the K₃AlF₆: Mn⁴⁺ phosphors were investigated. The results indicate that the phosphors prepared by this method consist of a single pure phase. By adjusting the molten salt content, the morphology of the product can be transformed from nanoparticle-like to nanorod-like structures. All products exhibit the characteristic red emission of Mn⁴⁺ under blue and violet light excitation, with the optimally doped sample achieving an internal quantum efficiency (IQE) of 69% under blue light excitation. The combination of the obtained K₃AlF₆: Mn⁴⁺ with the yellow phosphor YAG enabled the fabrication of W-LEDs. These W-LEDs achieved a color rendering index (Ra) of 86.8, a luminous efficacy (LE) of 77 lm/W, and a correlated color temperature (CCT) of 3690 K, along with excellent color stability under operating conditions. Full article

Thermal stability is a crucial factor in evaluating phosphors and determining whether they can be utilized in white light emitting diodes (w-LEDs). In this work, a series of Sr₆LuAl(BO₃)₆: Dy³⁺ (SLAB:Dy³⁺) phosphors was synthesized via high-temperature solid-state reaction. The synthesized SLAB:Dy³⁺ phosphor exhibits narrow-band emission in the range of 450–700 nm under 348 nm UV excitation. The strongest emission peak is located at 577 nm and is primarily due to ⁴F_9/2-⁶H_13/2 electron transitions. The optimal doping concentration of Dy³⁺ in the synthesized phosphor was 15 mol%. The integrated emission intensity of the synthesized phosphor at 480 k is 97.84% of that at 300 k, with excellent thermal stability. The activation energy E_g = 0.62 eV. Meanwhile, the Commission International de l’Eclairage (CIE) coordinates of the prepared w-LEDs were (0.309,0.363) with a correlated color temperature (CCT) of 6497 K. Preliminary experimental findings suggest that SLAB:Dy³⁺ phosphors hold promise for utilization in w-LEDs applications. Full article

Long persistent phosphors are widely used in many fields, such as LED, bioimaging, urgent lighting, temperature sensors, etc. Although green and blue long persistent phosphors are well developed, efficient orange-yellow long persistent phosphors are still relatively rare. In this work, a novel orange-yellow long-persistent phosphors Ca₂LuScGa₂Ge₂O₁₂:xPr³⁺ (CLSGGO:xPr³⁺, x = 0.003, 0.005, 0.01, 0.02, 0.03, 0.04, 0.05) are prepared and systematically investigated through its crystal structural information, photoluminescence, and persistent luminescence properties. Under ultraviolet light excitation, these phosphors exhibit orange-yellow emission stemming from the ³P₀ and ¹D₂ multiple electron transitions in the 4f level of Pr³⁺ ion. In addition, the material exhibits bright persistent luminescence. The complex garnet matrix structure of Ca₂LuScGa₂Ge₂O₁₂ provides excellent conditions for the formation of traps. Through the testing of thermoluminescence curve and function fitting, the density and depth of traps are studied; also, the storage and release process of carriers in the material are calculated in detail. A reasonable persistent luminescence mechanism is proposed for CLSGGO:0.01Pr³⁺. This work enriches the research content of photoluminescence and long persistent luminescence of Pr³⁺-doped garnet-based phosphors and paves the way for the future research of long persistent luminescent materials doped with rare earth ions. Full article

To reduce the time of postoperative recovery and to prevent post-surgical complications, biocompatible synthetic materials with osteoconductive and osteoinductive properties are used as bone substitutes in large bone defect management. A simplified biomimetic approach to similar materials is based on the use of an inorganic filler, a polymer matrix, and a compatibilizer, mimicking the composition of the natural bone. Based on plate-like micro-sized carbonated hydroxyapatite (pCAp), we prepared compression-molded samples optionally containing an additional polyester component (poly(ε-caprolactone) PCL, poly(L-lactide) PLLA, or poly(L-methylglycolide) PLMG); syntheticblock copolymers comprising fragments of the corresponding polyester and poly(ethylene phosphoric acid) (PEPA) were also prepared and studied asa ‘two-in-one’ polymer matrix/compatibilizer. Bone regeneration experiments involving a three-month rat tibial defect model were conducted with 250–500 μm granules of the composites. Comparative studies of the introduction of the polyester-b-PEPA copolymer into composites revealed a positive effect, which manifests itself in accelerated bone regeneration, which further intensified for pCAp/PEPA-b-PLMG. The latter composite formulation was used to study the results of the introduction of cerium into the filler. One-month experiments with pCAp, CePO₄-doped pCAp, and composites of these inorganic fillers with PEPA-b-PLMG were conducted. For the first time, a positive synergistic effect of the presence of cerium and PEPA in the composite, which appeared in substitution of the implant material by two-thirds of newly formed partly matured bone, was observed four weeks after surgery. Full article

In this work, systematic first-principles calculations were performed to investigate the multiband emissions of Bi-doped Y₃Ga(Al)₅O₁₂ phosphors. The predicted emissions of Bi³⁺ show that the violet narrow-band emission can be attributed to the ³P₁–¹S₀ transition of Bi³⁺ at Y sites, and both the metal-to-metal charge transfer (MMCT) of Bi³⁺ at Ga (Al) sites and the luminescence of Bi³⁺ dimers can generate visible emissions. Detailed formation energy calculations subsequently rule out the possibility that the visible emission originates from the MMCT of Bi³⁺ at Ga (Al), as the concentration of Bi_Y is much greater than that of B_Ga (or Bi_Al). To better understand the relationship between the nephelauxetic effect and the coordination environment, the vacuum-referred binding energy (VRBE) model was utilized to determine the energy levels of bismuth ions relative to the vacuum level in different systems and at different sites. The results provide insight into the relationship between the coordination environment and the emission properties of Bi³⁺ and are helpful for analyzing and optimizing the luminescent properties of bismuth-doped garnet-like materials. Full article

Confronted with increasing global food demands, diminishing arable land, and climate volatility, controlled-environment agriculture with advanced red and far-red LED lighting can enhance photosynthesis and optimize plant growth. This investigation reports the generation of a Mn⁴⁺/Nd³⁺ co-doped Y₂SiO₅ phosphor with a Nd³⁺ concentration ranging from 0.1 to 2.5 mol% via a solid-state synthesis method, aiming to enhance red and far-red emission for plant cultivation LEDs. For the Y₂SiO₅:Mn⁴⁺ (1 mol%), Nd³⁺ (2 mol%) phosphor, the phase integrity, nanostructured morphology, elemental mapping, and vibrational characteristics were examined using XRD, Rietveld analysis, FTIR, SEM, and EDX. Nd³⁺ ions act as near-infrared excitation mediators, ensuring efficient Nd³⁺ → Mn⁴⁺ energy transfer upon 808 nm excitation, and this leads to pronounced red photoluminescence from Mn⁴⁺ ions that covers the range of 640–710 nm, exhibiting strong emission peaks centered at 650nm, 663nm, and 685nm, coinciding with the absorption band of phytochromes and chlorophyll. The optimal emission intensity was accomplished for a Nd³⁺ doping concentration of 2 mol%, beyond which concentration quenching occurred. The material produced a strong, concentrated deep red emission with CIE coordinates near (0.73, 0.27) and a high color purity of 98.96%, making it well-suited for photosynthetic activation. A phosphor-integrated red pc-LED was fabricated, and Tulsi plants were grown under this LED during the winter in Meghalaya, a period critical for plant growth due to the low ambient light. Over a 30-day period, the plants exhibited enhanced height and leaf development, demonstrating the practical potential of Mn⁴⁺/Nd³⁺ co-doped Y₂SiO₅ for energy-efficient, wavelength-optimized horticultural lighting. Full article

Solution combustion-synthesized BaAl₂O₄: Eu²⁺, Nd³⁺, and Pr³⁺ blue–green long-afterglow phosphors are prepared and systematically investigated. First, XRD confirms the BaAl₂O₄ host and screens for trace residual features. SEM reveals the agglomerated granular morphology typical of combustion products. XPS verifies the valence states (Eu²⁺, Nd³⁺, Pr³⁺) and the chemical environment of the host lattice. UV-Vis diffuse reflectance spectra, transformed via the Kubelka–Munk function and analyzed using Tauc plots (indirect-allowed), indicate a wide band gap of the BaAl₂O₄ host with small, systematic shifts upon Nd³⁺/Pr³⁺ co-doping. PL measurements show Eu²⁺ 4f–5d emission and co-dopant-assisted excitation/defect pathways without altering the Eu²⁺ emission band shape. Afterglow lifetime and decay analyses correlate trap depth/distribution with the extended persistence. Finally, we demonstrate anti-counterfeiting by (i) snowflake printing and (ii) a binary 3 × 3 grid printed with two afterglow inks of different lifetimes to realize multi-level authentication. The sequential evidence links structure, chemistry, optical absorption, carrier trapping, and practical readout, providing a coherent basis for performance enhancement and application. Full article

A novel long-lasting luminescent composite material based on the (Ca,Sr)-Al-O system was synthesized using a solution combustion method. (Ca,Sr)₃Al₂O₆ is the primary phase, with SrAl₂O₄ as a controllable secondary phase. Compared to conventional single-phase SrAl₂O₄ phosphors, the introduction of a calcium-rich hexaaluminate matrix creates additional defects and a specific trap distribution at the composite interface, significantly improving carrier storage and release efficiency. Eu²⁺ + Nd³⁺ synergistic doping enables precise control of the trap depth and number. Under 365 nm excitation, Eu²⁺ emission is located at ~515 nm, with Nd³⁺ acting as an effective trap center. Under optimal firing conditions at 700 °C (Eu²⁺ = 0.02, Nd³⁺ = 0.003), the afterglow lifetime exceeds 30 s. Furthermore, The (Ca,Sr)₃Al₂O₆ host stabilizes the lattice and optimizes defect states, while synergizing with the SrAl₂O₄ secondary phase to improve the afterglow performance. This composite phosphor exhibits excellent dual-mode anti-counterfeiting properties: long-lasting green emission under 365 nm excitation and transient blue-violet emission under 254 nm excitation. Based on this, a screen-printing ink was prepared using the phosphor and ethanol + PVB, enabling high-resolution QR code printing. Pattern recognition and code verification can be performed both in the UV on and off states, demonstrating its great potential in high-security anti-counterfeiting applications. Compared to traditional single-phase SrAl₂O₄ systems, this study for the first time constructed a composite trap engineering of the (Ca,Sr)₃Al₂O₆ primary phase and the SrAl₂O₄ secondary phase, achieving the integration of dual-mode anti-counterfeiting functionality with a high-resolution QR code fluorescent ink. Full article

YVO₄ based phosphors have aroused extensive interest in the field of optoelectronics due to their good chemical stability and unique luminescence properties. However, commercialization of YVO₄ phosphors requires high luminescence intensity, enhanced conversion efficiency, and a wide excitation spectrum. In this work, Eu³⁺, Ba²⁺, Bi³⁺ co-doped YVO₄ was prepared by the sol–gel method. The XRD of YVO₄: 5%Eu³⁺, 5%Ba²⁺, 0.5%Bi³⁺ phosphor analysis confirms the pure tetragonal phase, with a fairly large size of approximately 100 nm for the optimal composition. And the SEM and TEM revealed well-dispersed spherical nanoparticles with sizes of 100–120 nm. The introduction of Ba²⁺ ions enhanced the luminescence intensity, while the incorporation of Bi³⁺ ions improved the excitation width of the phosphor. The resulting YVO₄: 5%Eu³⁺, 5%Ba²⁺, 0.5%Bi³⁺ phosphor exhibited a 1.39-times broader excitation bandwidth and a 2.72-times greater luminescence intensity at 618 nm compared to the benchmark YVO₄: 5% Eu³⁺ sample. Additionally, the transmittance of the films in the 350 nm to 800 nm region exceeded 85%. The YVO₄: 5%Eu³⁺, 5%Ba²⁺, 0.5%Bi³⁺ film effectively absorbed ultraviolet light and converted it to red emission, enabling potential applications in solar cell window layers, dye-sensitized cell luminescence layers, and solar cell packaging glass. Full article

Multifunctional phosphors that integrate optical temperature measurement and counterfeit detection capabilities have garnered considerable interest owing to their diverse application potential. In this study, novel CaLaLiTeO₆:Mn⁴⁺/Er³⁺ phosphors were prepared via the high-temperature solid-phase method. The phase structure and morphology characterization confirmed the successful synthesis of CaLaLiTeO₆ material with effective doping of Mn⁴⁺ and Er³⁺ into the host lattice. Upon excitation at 379 nm, the CaLaLiTeO₆:Mn⁴⁺/Er³⁺ material exhibits far-red emission at 716 nm (Mn⁴⁺:²E_g → ⁴A_2g) and green emission at 525/548 nm (Er³⁺:²H_11/2/⁴S_3/2 → ⁴I_15/2). The emission peak intensities of Er³⁺ and Mn⁴⁺ ions in the CaLaLiTeO₆:0.015Mn⁴⁺/0.01Er³⁺ sample displayed distinct variations with temperature under different excitation wavelengths (325 nm, 379 nm, and 980 nm). Subsequently, a dual-mode optical temperature sensing system was developed based on the fluorescence intensity ratio and the dual excitation single-band ratiometric method, which achieved a maxed relative sensitivity of 1.12% K⁻¹ at 343 K. Moreover, the excitation-dependent luminescence color changes of CaLaLiTeO₆:Mn⁴⁺/Er³⁺ make it particularly suitable for anti-counterfeiting applications. The present study underscores the dual-functional capabilities in sophisticated non-contact optical temperature measurement and anti-counterfeiting applications. Full article

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) offer distinct advantages over their low-temperature counterparts. However, their commercial viability is significantly hampered by durability challenges stemming from electrocatalyst support degradation in the corrosive phosphoric acid environment. This review provides a comprehensive analysis of advanced strategies to overcome this critical durability issue. Two main research directions are explored. The first involves engineering more robust carbon-based materials, including graphitized carbons, carbon nanostructures (nanotubes and graphene), and heteroatom-doped carbons, which enhance stability by modifying the carbon’s intrinsic structure and surface chemistry. The second direction focuses on replacing carbon entirely with intrinsically stable non-carbonaceous materials. These include metal oxides (e.g., TiO₂, SnO₂), transition metal carbides (e.g., WC, TiC), and nitrides (e.g., Nb₄N₅). For these non-carbon materials, a key focus is on overcoming their typically low electronic conductivity through strategies such as doping and the formation of multi-component composites. The analysis benchmarks the performance and durability of these advanced supports, concluding that rationally designed composite materials, which combine the strengths of different material classes, represent the most promising path toward developing next-generation, long-lasting catalysts for HT-PEMFCs. Full article

Mg₂TiO₄:Mn⁴⁺ (MTO:Mn⁴⁺) red phosphor has important applications in areas such as red LEDs and forensic science, but the preparation of MTO:Mn⁴⁺ through the solid-state reaction method requires a high sintering temperature. Herein, MTO:Mn⁴⁺ red phosphor was synthesized using the solid-state reaction method with LiCl flux, and its crystallographic structure and photoluminescence properties were studied to determine the influence of experimental parameters like the amount of fluxing agent added and sintering temperature in producing a bright red phosphor suitable for LEDs. The experimental results showed that samples with added LiCl could form pure MTO after sintering at 950 °C, whereas those without LiCl still contained a mixture of MTO and MgTiO₃, even when sintered at 1400 °C. The optimal performance was achieved with a sample doped with 0.2 mol% Mn⁴⁺, synthesized using 50 wt% LiCl flux and sintered at 950 °C for 12 h. This sample exhibited a broad excitation band and a narrow red emission band peaking at 662 nm, confirming its excellent luminescence properties. Furthermore, a prototype red LED fabricated with a 377 nm chip and MTO:0.2% Mn⁴⁺ phosphor achieved photoelectric conversion efficiency of 78.5% at a 100 mA drive current, confirming its viability for high-performance red LED manufacturing. Full article

Lanthanide-doped inorganic luminescent materials have been extensively studied and applied in X-ray detection and imaging, anti-counterfeiting, and optical information storage. However, many reported rare-earth-based luminescent materials show only single-mode optical responses, which limits their applications in complex scenarios. Here, we report a novel Na₃KMg₇(PO₄)₆:Eu phosphor synthesized by a simple high-temperature solid-state method. The multi-color luminescence of Eu²⁺ and Eu³⁺ ions in a single matrix of Na₃KMg₇(PO₄)₆:Eu, known as radio-photoluminescence, is achieved through X-ray-induced ion reduction. It demonstrated a good linear response (R² = 0.9897) and stable signal storage (storage days > 50 days) over a wide range of X-ray doses (maximum dose > 200 Gy). In addition, after X-ray irradiation, this material exhibits photochromic properties ranging from white to brown in a bright field and shows remarkable bleaching and recovery capabilities under 254 nm ultraviolet light or thermal stimulation. This dual-modal luminescent phosphor Na₃KMg₇(PO₄)₆:Eu, which combines photochromism and radio-photoluminescence, presents a dual-mode X-ray detection and imaging strategy and offers a comprehensive and novel solution for applications in anti-counterfeiting and optical information encryption. Full article

In this paper, we study the temperature- and emission wavelength-dependent time responses of previously reported precursor-driven Eu²⁺- and Dy³⁺-doped strontium-aluminate phosphors to create unique luminescent anti-counterfeiting tags suitable for detection with smartphones. A smartphone was used to detect the red–green–blue (RGB) components of the rise and decay time responses of the samples in a temperature range from 0 °C to 100 °C. The RGB color-dependent detection revealed a finer excitation/relaxation kinetics structure of the individual samples, which becomes evident in the decay responses. The results suggest another possibility for multilevel encoding and temperature sensor applications, and provides a foundation for developing a more accurate theoretical model of the energy transitions in phosphorescent materials. Full article

High-Temperature Proton-Exchange Membrane Fuel Cells (HT-PEMFCs) represent a promising clean energy technology and are valued for their fuel flexibility and simplified balance of plant. Their commercialization, however, is critically hindered by the prohibitive cost and resource scarcity of platinum-group metal (PGM) catalysts. The challenge is amplified in the phosphoric acid (PA) electrolyte of HT-PEMFCs, where the severe anion poisoning of PGM active sites necessitates impractically high catalyst loadings. This review addresses the urgent need for cost-effective alternatives by providing a comprehensive assessment of recent advancements in non-precious metal (NPM) catalysts for the oxygen reduction reaction (ORR) in HT-PEMFCs. It systematically explores synthesis strategies and structure–performance relationships for emerging catalyst classes, including transition metal compounds, metal–nitrogen–carbon (M-N-C) materials, and metal-free heteroatom-doped carbons. A significant focus is placed on M-N-C catalysts, particularly those with atomically dispersed Fe-Nx active sites, which have emerged as the most viable replacements for platinum due to their high intrinsic activity and notable tolerance to phosphate poisoning. This review critically analyzes key challenges that impede practical application, such as the trade-off between catalyst activity and stability, mass transport limitations in thick electrodes, and long-term degradation in the harsh PA environment. Finally, it outlines future research directions, emphasizing the need for a synergistic approach that integrates computational modeling with advanced operando characterization to guide the rational design of durable, high-performance catalysts and electrode architectures, thereby accelerating the path to commercial viability for HT-PEMFC technology. Full article