Luminescence Properties Research Articles

Synthesis and luminescence study of the rare earth ion (Nd3+) doped Sr3Bi(PO4)3 phosphor

Results of a first investigations on luminescence in Nd[Formula: see text] doped Sr3Bi(PO4)3 are presented. Typical emission is in near infrared (NIR) region consisting of lines attributable to f–f transitions. The excitation also comes from f–f transitions involving higher energy levels, spanning a broad spectral range starting from near ultraviolet (nUV) running through NIR. As much as 5[Formula: see text]mol.% of Nd[Formula: see text] could be doped before concentration quenching of luminescence set in. The quenching was attributed to energy transfer between Nd[Formula: see text] ions taking place through a multipolar mechanism; the critical distance being 21.64[Formula: see text]Å. An easy synthesis method involving low-cost chemicals and favorable luminescence properties makes this phosphor a potential candidate for NIR applications.

Toward Monolayered Solar Cells: Luminescence Properties and Light Soaking in TMDs.

The optical and photonic characteristics of monolayer transition metal dichalcogenides (TMDs) play a pivotal role in their functionality as solar cell materials, light-emitting diodes (LEDs), and other electro-optical applications. In this study, we reveal the impact of prolonged illumination on the luminescence properties and Raman spectra of monolayered MoS2 and WS2─a process known as "light soaking". We find a light-induced transition from the physisorption to the chemisorption of ambient O2 and H2O molecules. In parallel, we observe the activation and passivation of defect sites in the samples (depending on their initial defect density), which is attributed to the adsorbed ambient molecules and the resulting light-driven interactions with defect sites. Thus, we can control the active defect density of monolayered TMDs and shed light on the fundamental mechanisms underlying their luminescence properties. Therefore, this work clarifies the source of changes to the luminescence properties of TMDs and opens the path toward their integration into advanced applications that may be affected by light soaking, such as solar cells and energy devices.

Dy3+ doped KCa(PO3)3 phosphor for white light generation: structural and luminescent studies

Abstract Using the traditional solid-state reaction approach, Dy3+ ions doped KCa(PO3)3 phosphors have been synthesized to investigate their luminescent properties to produce high-quality white light for solid-state lighting applications, particularly in white LEDs. X-ray diffraction (XRD) patterns were used to examine the structure and phase of the phosphors. Using scanning electron microscopy (SEM), the morphology of the as-synthesized phosphor has been investigated. Fourier transform infrared spectroscopy (FT-IR) has been used to investigate several vibrational bands seen in the phosphor. Using diffuse reflectance spectra (DRS), the as-synthesized phosphors' optical band gap values have been estimated. When Dy3+ ions are excited at 350 nm, the photoluminescence (PL) spectra characteristics observed for the activated KCa(PO3)3 phosphor show strong white area emission at 575 nm, which is related to the 4F99/2 → 6H13/2 transition of Dy3+ ions. Additionally, the concentration quenching of Dy3+ ions doped at 4 mol% is seen in the PL spectra. Based on the observed PL spectra, the computed CIE chromaticity coordinates for the doped KCa(PO3)3 phosphors show that the optimised 4.0mol% Dy3+ doped phosphor is located in the deep white area. The lifespan of the as-titled phosphors decreases as the amount of Dy3+ ions increases in the host lattice. Additionally, the PL decay profiles shows a dual exponential behaviour when excited at 350 nm, with an emission wavelength at 575 nm. On the basis of the results of the aforementioned studies, we wish to project Dy3+ ion doped KCa(PO3)3 phosphors as white light generating materials in w-LEDs and for other photonic applications.

Структура, ріст та оптичні характеристики монокристалів сульфанілату гуанідинію (GSA)

Guanidine Sulphanilate (GSA) single crystal was grown by slow evaporation growth method. Single crystal X-ray diffraction studies show that the crystal grows in a centro symmetric monoclinic system and its space group is P21/c. Optical studies were carried out using UV visible spectroscopy and the grown crystal shows the the lower cutoff wavelength of 220 nm. Photoluminescence studies show that GSA crystals have good luminescence properties. Laser damage threshold was found to be 0.24GW/cm2. Nonlinear optical studies show green light emission.

Reversible Multi-Mode Optical Modification in Inverse-Opal-Structured WO3: Yb3+, Er3+ Photonic Crystal

Reversible optical regulation has potential applications in optical anti-counterfeiting, storage, and catalysis. Compared to common power materials, the reverse opal structure has a larger specific surface area and an increased contact area for optical regulation, which is expected to achieve higher regulation rates. However, it is difficult to achieve reversible and repeatable regulation of the luminescent properties of photonic crystals, especially with the current research on the structural collapse of photonic crystals. In this work, WO3: Yb3+, Er3+ inverse photonic crystals were prepared by the template approach, and reversible multi-mode optical modification was investigated. Upon heat treatment in a reducing atmosphere or air, the color of the photonic crystals can reversibly change from light yellow to dark green, accompanied by changes in absorption and upconversion of luminescence intensity. The stability and fatigue resistance of this reversible optical modification ability were explored through cyclic experiments, providing potential practical applications for photocatalysis, optical information storage, and electrochromism.

Enhanced luminescent properties of poly(sodium acrylate)-based composite and its selective interaction towards copper ions

This study investigates the luminescent properties and metal ion interactions of europium when combined with a polymer chain of poly (sodium acrylate) (PSA) and a phenanthroline (Phen) molecule, which acts as an efficient antenna. The study of interactions between lanthanide ions and various compounds in different matrices is crucial, providing valuable insights into the molecular environment, and enabling a deeper understanding of processes affecting their luminescence. In this study, we investigated the luminescent properties of the Eu(PSA)Phen complex and its remarkable capacity for selective interaction with Cu2+ ions in an aqueous solution. From this selective interaction, we conducted a series of detailed studies that provided valuable insights into the mechanisms of luminescence suppression, information about the europium chemical environment, and other related aspects. The luminescence of Eu(PSA)Phen is significantly quenched by Cu2+ ions, driven by both static and dynamic mechanisms. The presence of the PSA polymer chain and Phen molecules within the composite exerts a profound influence on energy transfer processes, enabling selective responses to Cu2+ ions, even in the presence of competing cations. Additionally, we observed a preferential interaction of the PSA molecule in the Eu(PSA)Phen composite with Cu2+ ions over the N groups of phenanthroline. These findings underscore the compound potential as a versatile tool in various fields, ranging from material science to biosensing, where rapid and selective metal ion detection is of paramount importance.

Far-red emitting Li2TiO3: Cr3+ phosphor: Synthesis, luminescence properties and potential applications

The Cr[Formula: see text]-activated phosphor can emit far-red light under the excitation of an external light source, mainly due to the transition of the outermost electrons of Cr[Formula: see text] from the 2E level to the 4A2 level in a strong crystal field environment. A novel far-red Li2TiO3: Cr[Formula: see text] phosphor was prepared by the solid-state method. Under the excitation of 356[Formula: see text]nm, the Li2TiO3: Cr[Formula: see text] phosphors emit intense far-red light in 600–850[Formula: see text]nm with a central wavelength of 732[Formula: see text]nm. The emission band of all samples was matched with the absorption bands of phytochrome P[Formula: see text]. The experimental data and theoretical calculation confirmed that Cr[Formula: see text] is surrounded by a strong crystal field environment. The effect of Cr[Formula: see text] doping concentration on the luminescence intensity was analyzed. These research works demonstrate that far-red Li2TiO3: Cr[Formula: see text] phosphors have potential applications in plant growth lights.

Effect of Post-Implantation Heat Treatment Conditions on Photoluminescent Properties of Ion-Synthesized Gallium Oxide Nanocrystals

A novel and promising way for creating nanomaterials based on gallium oxide is the ion synthesis of Ga2O3 nanocrystals in a SiO2/Si dielectric matrix. The properties of nanocrystals are determined by the conditions of ion synthesis—the parameters of ion irradiation and post-implantation heat treatment. In this work, the light-emitting properties of Ga2O3 nanocrystals were studied depending on the temperature and annealing atmosphere. It was found that annealing at a temperature of 900 °C leads to the appearance of intense luminescence with a maximum at ~480 nm caused by the recombination of donor–acceptor pairs. An increase in luminescence intensity upon annealing in an oxidizing atmosphere is shown. Based on data from photoluminescence excitation spectroscopy and high-resolution transmission electron microscopy, a hypothesis about the possibility of the participation of a quantum-size effect during radiative recombination is proposed. A mechanism for the formation of Ga2O3 nanocrystals during ion synthesis is suggested, which makes it possible to describe the change in the luminescent properties of the synthesized samples with varying conditions of post-implantation heat treatment.

Luminescent Alendronic Acid-Conjugated Micellar Nanostructures for Potential Application in the Bone-Targeted Delivery of Cholecalciferol

Vitamin D, an essential micronutrient crucial for skeletal integrity and various non-skeletal physiological functions, exhibits limited bioavailability and stability in vivo. This study is focused on the development of polyethylene glycol (PEG)-grafted phospholipid micellar nanostructures co-encapsulating vitamin D3 and conjugated with alendronic acid, aimed at active bone targeting. Furthermore, these nanostructures are rendered optically traceable in the UV–visible region of the electromagnetic spectrum via the simultaneous encapsulation of vitamin D3 with carbon dots, a newly emerging class of fluorescents, biocompatible nanoparticles characterized by their resistance to photobleaching and environmental friendliness, which hold promise for future in vitro bioimaging studies. A systematic investigation is conducted to optimize experimental parameters for the preparation of micellar nanostructures with an average hydrodynamic diameter below 200 nm, ensuring colloidal stability in physiological media while preserving the optical luminescent properties of the encapsulated carbon dots. Comprehensive chemical-physical characterization of these micellar nanostructures is performed employing optical and morphological techniques. Furthermore, their binding affinity for the principal inorganic constituent of bone tissue is assessed through a binding assay with hydroxyapatite nanoparticles, indicating significant potential for active bone-targeting. These formulated nanostructures hold promise for novel therapeutic interventions to address skeletal-related complications in cancer affected patients in the future.

Solid-state excimer emission of o-carborane derivatives and applications for stimuli-responsive luminescent materials.

o-Carborane is an icosahedral cluster containing boron and has been paid attention as a versatile platform for constructing stimuli-responsive materials with solid-state luminescence properties by suppressing aggregation-caused quenching (ACQ), which is the emission annihilation process observed in condensed states, such as concentrated solutions, solids and films. Non-specific intermolecular interactions in the condensed states resulting in ACQ are disturbed by the spherical boron cluster. More recently, it has been demonstrated from several reports that o-carborane is capable of assisting solid-state excimer emission in aryl-modified o-carboranes. Moreover, some of these materials provide unique stimuli-responsiveness. In the commodity design for solid-state luminescent materials, o-carboranes are responsible for disturbing intermolecular interactions and subsequently presenting solid-state luminescence. On the other hand, excimer emission, which is inducible from the intermolecular photophysical process, has been discovered in the solid state based on o-carborane materials. In this manuscript, recent progress in stimuli-responsive luminescent materials via excimer formation will be described. Moreover, as the further potential of o-carborane materials, recent findings on the photo-salient effect which can be induced through excimer formation followed by photoreaction will also be explained.

Dual-stimuli-responsive Turn-on Luminescence of Chiral Bisimidazolyl BINOL Dimethyl Ether Crystals.

Stimuli-responsive organic luminescent crystals have attracted significant attention in recent years for their potential in sensor and memory applications. While turn-on luminescence is superior in detection sensitivity compared with turn-off luminescence, the development of organic crystals that exhibit turn-on luminescence in response to multiple stimuli remains a significant challenge. Herein, the crystals of chiral bisimidazolyl 1,1'-bi-2-naphthol (BINOL) dimethyl ether have exhibited a dual-stimuli-responsive turn-on luminescence based on two distinct mechanisms. In the crystalline state, luminescence was substantially quenched by the intermolecular hydrogen bonds between the imidazole rings. Mechanical stimulation induced a transition to a blue-violet-emissive amorphous state. In contrast, thermal stimulation produced an orange luminescence, attributed to excited-state intramolecular proton transfer (ESIPT) luminescence from thermally demethylated products. Furthermore, the thermally induced state exhibited circularly polarized luminescence (CPL), marking a rare instance of stimuli-responsive turn-on CPL in a solid-state system. This study provides new insights into environmental and structural factors for solid-state luminescent properties and advances the design guidelines for multifunctional luminescent sensors.

Micrometric patterning of a borogermanate glass containing terbium by thermal poling to manage luminescence and second order optical properties

Micrometric patterning of a borogermanate glass containing terbium by thermal poling to manage luminescence and second order optical properties

Effects of doping with selected rare-earth elements (Eu3+, Dy3+, Eu3+/Dy3+) on the structural characteristics as well as electrical and luminescent properties of K0.5Na0.5NbO3

The effects of adding Eu3+, Dy3+, and Eu3+/Dy3+ rare-earth elements on the microstructural, optical and electrical properties of lead-free piezoelectric materials based on K0.5Na0.5NbO3 (KNN) were investigated. A series of fine powders were synthesized via a modified Pechini route utilizing citric acid. Relatively large amounts of rare-earth elements were successfully incorporated into the crystal lattice of KNN. A combination of X-ray diffraction, X-ray absorption spectroscopy, energy-dispersive X-ray and scanning electron microscopy were used to characterize the structure and chemical composition of the powders and sinters. XRD patterns indicated the formation of a single-phase orthorhombic structure in the co-doped sinter. X-ray absorption spectroscopy revealed the nominal 3+ valence states of Eu and Dy in KNN ceramic sinters. The Mott model and group symmetry theory were used to discuss the characteristics of Raman spectra obtained for the EuDy:KNN ceramics. The ceramics exhibited good dielectric permittivity (ε≃1300) and low dielectric loss (tan δ=0.03) in the temperature range of 170–240°C. The electrical properties of the ceramics showed that the basic mechanism of conduction and relaxation was thermal activation, and that small polaron hopping was responsible for charge carrying. The Eu3+ and Dy3+ ions displayed characteristic red and orange emissions in sinters when excited with light in the wide ultraviolet spectra range (380–420 nm).

Integrating K+ into Eu and Tb doped GdCa4O(BO3)3: A dual study on photoluminescence and structure

In this study, we investigate the structural and photoluminescence (PL) properties of rare-earth-doped GdCa4O(BO3)3 (GdCOB) phosphors, specifically focusing on the spectral behaviour induced by doping with Eu³⁺ and Tb³⁺ ions. The powder X-ray diffraction (XRD) spectra confirm the formation of a monoclinic phase. The XRD data were also refined by a Rietveld refinement method. The existence of B, O, Ca, Gd, Tb, Eu and K elements was verified by EDS spectra. We introduce a detailed examination of the charge compensation process using Kröger-Vink notation to clarify the mechanisms essential for tailoring the optical properties of the phosphors. The PL excitation spectrum of GdCOB:Eu3+, monitored at 611 nm, reveals sharp excitation peaks at 319, 361, 380, and 392 nm, corresponding to 7F0→5H3, 7F0→5D4, 7F0→7F0, and 7F0→5L6 transitions, respectively. The PL spectrum under excitation of 392 nm exhibits that phosphors doped with Eu3+ a significant red emission at 611 nm, which is attributed to the 5D₀→7F₂ transition. This emission intensity is particularly enhanced at non-centrosymmetric sites of the Eu³⁺ ions. Similarly, the PL excitation spectrum of GdCOB:Tb3+, monitored at 552 nm, displays distinct excitation peaks at 316, 341, 353, and 379 nm, which correspond to the transitions 7F₆→5D₀, 7 F₆→5L₇, 7F₆→5D₂, and 7F₆→5D₃, respectively. Tb³⁺-doped phosphors display a bright green emission, with a dominant peak at 552 nm, resulting from the 5D₄→7F₅ transition. Additionally, the introduction of K⁺ ions as co-dopants results in modifications to the local environments of Eu³⁺ and Tb³⁺ ions. These changes allow for fine-tuning of the emission peaks, significantly enhancing the luminescent output of the phosphors. Optimal doping concentrations of 5 mol% for Eu³⁺ and 1 mol% for Tb³⁺ enhance luminescent intensity and prevent concentration quenching. This phenomenon, often resulting in reduced PL intensity at higher dopant levels, is primarily due to dipole-dipole interactions, consistent with Dexter's theory of energy transfer. Strategic modulation of doping concentrations, coupled with a deep understanding of energy transfer mechanisms are critical for the development of advanced luminescent materials Our analysis of the Commission de l′Eclairage (CIE) chromaticity coordinates reveals enhanced energy transfer dynamics in rare-earth-doped borates, facilitating the tuning of luminescent properties. These results not only deepen our understanding of the fundamental physics governing such phosphors but also open pathways for the development of optoelectronic applications requiring consistent color output, such as LED technologies and solid-state lighting.

Luminescence properties of Eu3+ complexes based on macrocyclic ligands and its colorimetric analysis for white warm phosphor

Luminescence properties of Eu3+ complexes based on macrocyclic ligands and its colorimetric analysis for white warm phosphor

Piperidine and isobutyl-nitrite fuels for the combustion synthesis of nanomaterials: A study of crystal structure, microstructure, thermodynamics, and optical properties

In this research, the fuels of piperidine (C5H11N) and isobutyl nitrite (C4H9NO2) were used to produce YVO4:Eu3+ nanoparticles. To remove the remaining organic materials and also to improve the crystal structure, these materials were calcined at 800 and 1000 °C, and then the particle size and morphology of the synthesized nanostructures were monitored using a scanning electron microscope (SEM). It was found that the type of consumed fuel and also the calcination temperature result in significant effects on the morphology of the nanostructures as well as the obtained luminescence properties. The use of isobutyl nitrite and piperidine leads to synthesis of homogeneous powders with particle sizes of 38 and 100 nm, respectively. The Rietveld calculations revealed that the growth of the mentioned particles through calcination at 800 °C leads to a reduction of microstrains from 0.00137 to 0.00048 and 0.00126 to 0.00044, respectively. The exciting of these materials by the wavelength of 307 nm causes the creation of a powerful emission spectrum with the highest intensities at the wavelengths of 594 and 624 nm, which originate from the electron transitions of 5D0–7F1 and 5D0–7F2, respectively. Also, the photoluminescence emission of phosphors synthesized by isobutyl nitrite is higher than that of piperidine, which this phenomenon is consistent with X-ray diffraction (XRD) and thermo-gravimetric analysis (TGA) results which proved that the crystallinity of the phosphors synthesized by isobutyl nitrite is higher than that of piperidine.

Synthesis, structure and photoluminescence properties of heterometallic-based coordination polymers of trimesic acid.

Reacting trimesic acid (H3TMA, C9H6O6) with CaCl2 and MCl2 at 110 °C under hydrothermal conditions gave the isostructural heterobimetallic coordination polymers (CPs) catena-poly[[tetraaquazinc(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaZn(HTMA)2(H2O)8]n, 1, and catena-poly[[tetraaquacobalt(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaCo(HTMA)2(H2O)8]n, 2. Compounds 1 and 2 crystallize in the monoclinic space group C2/c. The solid-state structures consist of eight-coordinate CaII ions and six-coordinate MII ions. These ions are connected by a doubly deprotonated HTMA2- ligand to create a one-dimensional (1D) zigzag chain. Poly[[decaaquabis(μ3-benzene-1,3,5-tricarboxylato)calcium(II)dizinc(II)] dihydrate], {[CaZn2(TMA)2(H2O)10]·2H2O}n, 3, was found incidentally as a minor by-product during the synthesis of 1 at a temperature of 140 °C. It forms crystals in the orthorhombic space group Ccce. The structure of 3 consists of a two-dimensional (2D) layer composed of [Zn(TMA)] chains that are interconnected by CaII ions. The presence of aromatic carboxylic acid ligands and water molecules, which can form numerous hydrogen bonds and π-π interactions, increases the stability of the three-dimensional (3D) supramolecular architecture of these CPs. Compounds 1 and 2 exhibit thermal stability up to 420 °C, as indicated by the thermogravimetric analysis (TGA) curves. The powder X-ray diffraction (PXRD) data reveal the formation of unidentified phases in methanol and dimethyl sulfoxide, while 1 exhibits chemical stability in a wide range of solvents. The luminescence properties of 1 dispersed in various low molecular weight organic solvents was also examined. The results demonstrate excellent selectivity, sensitivity and recyclability for detecting acetone molecules in aqueous media. Additionally, a possible sensing mechanism is also outlined.

Optically stimulated luminescence properties of In-doped CsBr transparent ceramics

0.01, 0.1, 0.5, and 1% In-doped CsBr transparent ceramics were synthesized by the spark plasma sintering method. Their photoluminescence and optically stimulated luminescence (OSL) properties were evaluated. All the samples showed transparency with transmittances of 40–60%. Luminescence due to 3P1–1S0 transitions of In + appeared at 500 nm. OSL emission peaks were confirmed at 500 nm upon constant stimulation light at 630 nm. A 0.1% In-doped sample showed the highest OSL intensities in prepared samples and the dose-response relationship was linear from 0.01 to 1000 mGy. The spatial resolution of X-ray images was confirmed from 5.00 LP/mm by using OSL of a 0.1% In-doped sample.

Modulation of components toward blue light emission and scintillation properties of Eu2+ activated Sr1-xLaxMgxAl12-xO19 crystal

The development of Eu2+-activated oxide materials with high efficiency, fast decay and narrow bandwidth emission in the visible region is still challenging for the field of luminescence and scintillation applications. Generally, Eu2+ in oxide hosts can emit intense and broad 5d-4f emission in the visible region, but efficient emitting with stable bivalence of Eu is rare in inorganic oxide system. In this work, a series of ASL:Eu2+ (Sr1-xLaxMgxAl12-xO19) powder samples with various La, Mg doping ratios were designed and synthesized to modulate the UV or X-ray excited luminescence properties, including redshift, quantum yield, and decaying lifetime. Moreover, an ASL:Eu2+ crystal with the optimal ratio x = 1/3 was grown, its scintillation performance was compared with standard Bi4Ge3O12 crystal sample and evaluated in detail. These results indicate that the ASL:Eu2+ crystal is potential scintillator as a kind of X-ray detection and provide a reference for the further development of high-performance Eu-activated oxide scintillation materials.

Luminescence properties of SrB6O10:Ce,Gd phosphor for applications in OSL dosimetry and lighting

Strontium hexaborate (SrB6O10) doped with different metals and/or lanthanides has been studied widely as the thermoluminescence (TL) dosimeter. However, there is almost no dosimetry study concerning the utility of Optically Stimulated Luminescence (OSL) on SrB6O10. This preliminary study aims to examine the luminescence properties of SrB6O10 phosphor for their application in the areas of dosimetry and lighting technologies. Undoped and doped material to get an OSL dosimeter were synthesized by incorporating the dopants Ce3+, in the range of 0.1–0.7 % wt, and Gd3+, in the range of 0.1–1 % wt into the SrB6O10 structure using the solution combustion (SCS) method. The structural and morphological characterizations were performed using X-ray diffraction (XRD) and Scanning Electron Microscope (SEM) methods, respectively. Two TL peaks of SrB6O10:Ce0.1%,Gd0.5% occurred at 70 °C and 182 °C after 1 Gy exposure to beta rays with a heating rate of 2 °C/s. The step annealing measurements were carried out to determine the traps responsible for the OSL signal. Various properties of the luminophore including dose-response and reusability were investigated using blue light stimulation. The phosphor showed a little variation of response up to 20 cycles within 2 % deviation (STD) from the first OSL readout. The OSL output within the range of 2–20 Gy was determined as linear. Radioluminescence (RL) measurement was investigated by emission in the range λem = 200–1000 nm. The parent compound displayed UV emission subdivided into UVA (315–400 nm), and UVB (280–315 nm) emissions at room temperature. The Chromaticity Coordinates (CIE) of SrB6O10:Ce0.1%,Gd0.5% were calculated as x = 0.2165, y = 0.1767. These remarkable characteristics show that, if developed, SrB6O10 could be used as an OSL dosimeter.