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A Silicotungstate-Based Silver(I) Compound with Octanuclear Core: Synthesis, Crystal Structure and Luminescent Property
摘要： A novel silicotungstate-based silver(I) compound, formulated as [{Ag8(H3mtz)12}{SiW12O40}2]·8H2O (1) (H3mtz = 3-Mercapto-1,2,4-triazole) has been hydrothermally synthesized. This compound was identified by the single-crystal X-ray diffraction, and also characterized by FT-IR, UV, TG, PXRD and elemental analyses. The data show that it possesses the octanuclear silver(I) clusters and the anionic silicotungstates, which were connected via the hydrogen bonds and weak Ag–O bonds. Interestingly, the estimated optical bandgap of compound 1 is 1.95 eV, which falls into the range of semiconductors.
关键词： Polyoxometalate,Crystal structure,Luminescence,Silver(I)-based cluster
更新于2025-09-23 15:22:29
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Investigation of energy transfer in Pr3+, Yb3+ co-doped phosphate phosphor: the role of 3P0 and 1D2
摘要： The synthesis, crystal structure and photoluminescence and decay kinetics properties have been carried out for the Pr3+-Yb3+ co-doped YPO4 phosphors. Upon excitation with 447 nm, the intense emissions from 3P0, 1D2 and 1G4 excited states are all observed in the Pr3+ singly doped phosphors. The population of 1D2 state is attributed to cross-relaxation 3P0 +3H4 → 1D2+3H6 and/or non-radiative multiphonon relaxation from 3P0 because of the larger maximum phonon energy of YPO4 host (1080 cm-1),which needs only 3-4 phonons to balance the energy gap between 3P0 and 1D2 excited states. For the Pr3+-Yb3+ codoped samples, the effect of Yb3+ concentration on the luminescence and decay kinetics of Pr3+ are investigated for the interpretation of observed experimental results. The observations and discussions manifest that the efficient energy transfer from Pr3+ to Yb3+ occurs, involving mainly 1D2 and 1G4 levels of Pr3+ ions instead of 3P0 level, which is not in accordance with many reported results. It is hoped that our results may give a new insights into the energy transfer mechanism in Pr3+-Yb3+ codoped system.
关键词： YPO4,luminescence decay,emission intensity,energy transfer
更新于2025-09-23 15:22:29
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Five new coordination polymers of s- and d-block metals: Structural diversities, magnetic properties and luminescence
摘要： In order to explore the metal ions-controlled syntheses of coordination polymers (CPs), the temperature and solvent ratio were fixed in the reaction processes. By selecting a series of s- and d-block metal ions, five new CPs, [ZnL0.5(H2O)2]n (1), [CoL0.5(H2O)2]n (2), [Mn(H2L)(H2O)2]n (3), [Ca(H2L)(H2O)2]n (4) and [Ba(H2L)(H2O)2]n (5), have been synthesized by employing a less-investigated oxalamide N,N′-bis(4-phthalic acid) (H4L) ligand. H4L shows very versatile coordination modes and leads to various frameworks, including isomorphous 2D grid-like layer based on M2O2 cores for 1 and 2, isomorphous 4-connected 3D PtS frameworks based on 1D [M(CO2)2]n chains for 3 and 4, and a 2D wave-like layer based on [BaO3]n chains for 5.2 and 3 reveal the antiferromagnetic and ferromagnetic properties, respectively, while 1, 4 and 5 possesses strong solid state luminescence.
关键词： Luminescence,Crystal structure,Crystal engineering,Coordination polymer,Magnetic property
更新于2025-09-23 15:22:29
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Shallow and deep trap levels in X-ray irradiated β-Ga2O3: Mg
摘要： The results of the investigation of thermostimulated luminescence (TSL) and photoconductivity (PC) of the X-ray irradiated undoped and Mg2+ doped β-Ga2O3 single crystals are presented. Three low-temperature peaks at 116 K, 147 K and 165 K are observed on the TSL glow curves of undoped crystals. The high-temperature TSL peaks at 354 K and 385 K are dominant in Mg2+ doped crystals. The correlation between doping with Mg2+ ions and the local energy levels of the intrinsic structural defects of β-Ga2O3, which are responsible for the TSL peaks and PC, is established. The nature of TSL peaks and the appropriate photoconductivity excitation bands are discussed.
关键词： Photoconductivity,β-Ga2O3,Single crystal,Activation energy,Trap levels,Thermostimulated luminescence
更新于2025-09-23 15:22:29
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Energy Transfer between Tm-Doped Upconverting Nanoparticles and a Small Organic Dye with Large Stokes Shift
摘要： Lanthanide-doped upconverting nanoparticles (UCNP) are being extensively studied for bioapplications due to their unique photoluminescence properties and low toxicity. Interest in RET applications involving UCNP is also increasing, but due to factors such as large sizes, ion emission distributions within the particles, and complicated energy transfer processes within the UCNP, there are still many questions to be answered. In this study, four types of core and core-shell NaYF4-based UCNP co-doped with Yb3+ and Tm3+ as sensitizer and activator, respectively, were investigated as donors for the Methyl 5-(8-decanoylbenzo[1,2-d:4,5-d']bis([1,3]dioxole)-4-yl)-5-oxopentanoate (DBD-6) dye. The possibility of resonance energy transfer (RET) between UCNP and the DBD-6 attached to their surface was demonstrated based on the comparison of luminescence intensities, band ratios, and decay kinetics. The architecture of UCNP influenced both the luminescence properties and the energy transfer to the dye: UCNP with an inert shell were the brightest, but their RET efficiency was the lowest (17%). Nanoparticles with Tm3+ only in the shell have revealed the highest RET efficiencies (up to 51%) despite the compromised luminescence due to surface quenching.
关键词： time-resolved luminescence,core shell UCNP,DBD dye,resonance energy transfer
更新于2025-09-23 15:22:29
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Spectroscopic Properties of Er3+-Doped Particles-Containing Phosphate Glasses Fabricated Using the Direct Doping Method
摘要： The effect of the incorporation of Er2O3-doped particles on the structural and luminescence properties of phosphate glasses was investigated. A series of different Er2O3-doped TiO2, ZnO, and ZrO2 microparticles was synthesized using soft chemistry and then added into various phosphate glasses after the melting at a lower temperature than the melting temperature. The compositional, morphological, and structural analyses of the particles-containing glasses were performed using elemental mapping by field emission-scanning electron microscopy (FE-SEM) with energy dispersive x-ray spectrometry (EDS) and x-ray diffraction (XRD). Additionally, the luminescence spectra and the lifetime values were measured to study the influence of the particles incorporation on the spectroscopic properties of the glasses. From the spectroscopic properties of the glasses with the composition 50P2O5-40SrO-10Na2O, a large amount of the Er2O3-doped particles is thought to dissolve during the glass melting. Conversely, the particles were found to survive in glasses with a composition 90NaPO3-(10 ? x)Na2O-xNaF (with x = 0 and 10 mol %) due to their lower processing temperature, thus clearly showing that the direct doping method is a promising technique for the development of new active glasses.
关键词： oxyfluoride phosphate glass,direct particle doping,Er2O3-doped particles,Er3+ luminescence property,phosphate glass
更新于2025-09-23 15:22:29
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Preparation and Luminescence Properties of Ba5Si8O21 Long Persistent Phosphors Doped with Rare-Earth Elements
摘要： The phosphors of formula Ba5Si8O21:Eu2+,Dy3+ were synthesized and studied in order to improve their properties. Their synthesis conditions were evaluated as a function of precursors, crucible composition, flux agents, dopants and temperatures. The samples were characterised by means of a systematic investigation through elemental, kinetic, mineralogical (both qualitative and quantitative), and morphological analysis. This study allows for a careful evaluation of the parameters that influence the formation and properties of Ba5Si8O21:Eu2+,Dy3+ phosphors. As for the synthesis conditions, the use of Na2SiO3, BaCO3 and NH4Cl as precursors was very important to reduce the temperature and time of synthesis. The reducing atmosphere produced with purified coal was cheaper and gave results similar to the more traditional gas mixture (H2/N2). At the end of this study, a phosphor with improved long persistent phosphorescence (LPP) characteristics was obtained with Ba/Si = 0.7, Eu/Si = 2.8 × 10?3 and Dy/Si = 3.6 × 10?3 following a 6 h-synthesis in a quartz crucible.
关键词： barium silicates,kinetic analysis,luminescence,quantitative phase analysis,phosphors
更新于2025-09-23 15:22:29
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Complexation of the Mycotoxin Cyclopiazonic Acid with Lanthanides Yields Luminescent Products
摘要： Cyclopiazonic acid (CPA) is a neurotoxin that acts through inhibition of the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA). CPA blocks the calcium access channel of the enzyme. The inhibition may involve the binding of CPA with a divalent cation such as Mg2+. The potential for CPA to act as a chelator also has implications for methods to detect this toxin. Certain of the lanthanide metals undergo a dramatic increase in luminescence upon coordination with small molecules that can transfer excitation energy to the metal. This report is the first to describe the coordination of CPA with lanthanide metals, resulting in a substantial enhancement of their luminescence. The luminescence expressed was dependent upon the type of lanthanide, its concentration, and the environment (solvent, water content, pH). Based upon the phenomenon, a competitive assay was also developed wherein terbium (Tb3+) and a series of metal cations competed for binding with CPA. With increasing cation concentration, the luminescence of the CPA/Tb3+ complex was inhibited. The chlorides of ten metals were tested. Inhibition was best with Cu2+, followed by Co2+, Al3+, Fe3+, Mn2+, Au3+, Mg2+, and Ca2+. Two cations in oxidation state one (Na+, K+) did not inhibit the interaction significantly. The interaction of CPA with lanthanides provides a novel recognition assay for this toxin. It also provides a novel way to probe the binding of CPA to metals, giving insights into CPA's mechanism of action.
关键词： mechanism of action,lanthanides,calcium-ATPase,luminescence,mycotoxin,cyclopiazonic acid
更新于2025-09-23 15:22:29
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Engineering Tunable Broadband Near-Infrared Emission in Transparent Rare-Earth Doped Nanocrystals-in-Glass Composites via a Bottom-Up Strategy
摘要： Applications of trivalent rare earth (RE3+)-doped light sources in solid-state laser technology, optical communications, biolabeling, and solar energy management have stimulated a growing demand for broadband emission with flexible tunability and high efficiency. Codoping is a conventional strategy for manipulating the photoluminescence of active RE3+ ions. However, energy transfer between sensitizers and activators usually induces nonradiative migration depletion that brings detrimental luminescent quenching. Here, a transparent framework is employed to assemble ordered RE3+-doped emitters to extend the emission spectral range by extracting photons from a variety of RE3+ ions with sequential energy gradient. To block migration-mediated depletion between different RE3+ ions, a nanoscopic heterogeneous architecture is constructed to spatially confine the RE3+ clusters via a 'nanocrystals-in-glass composite' (NGC) structure. This bottom-up strategy endows the obtained RE3+-doped NGC with high emission intensity (nearly one order of magnitude enhancement) and broadband near-infrared emission from 1300 to 1600 nm, which covers nearly the whole low-loss optical communication window. Most crucially, NGC is a versatile approach to design tunable broadband emission for the potential applications in high-performance photonic devices, which also provides new opportunities for engineering multifunctional materials by integration and manipulation of diverse functional building units in a nanoscopic region.
关键词： luminescence,rare earth doping,broadband emission,nanocrystals-in-glass composite,near-infrared emission
更新于2025-09-23 15:22:29
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Comparative study on blue-turquoise silicate apatite phosphors prepared via different synthesis routes
摘要： Different types of gel precursors were obtained via microwave-assisted precipitation, gel-combustion, sol–gel, and Pechini methods in order to prepare Ca2Y7.76Ce0.12Tb0.12(SiO4)6O2 phosphors with apatite structure. The processes involved during the thermal treatment of precursors were revealed by TGA– FT-IR coupling. ICP-OES reveals that the incorporation degree of dopants (Ce3+, Tb3+) in silicate lattice are close to theoretical values while Ca2+ and Y3+ values shows differences depending on the synthesis route. The phosphors composition, morphology, structure, and optical characteristics are revealed by SEM, XRD, FTIR, and luminescent investigations. Pure hexagonal apatite with crystallite size of 76.5 nm was identi?ed in sample prepared by gel-combustion, while cubic-Y2O3 and monoclinic-Y2SiO5, as secondary phases, were found in precipitated samples. The purity phase was enhanced by increasing the TEOS amount during precipitation. As a result of the Ce3+ incorporation into different symmetry sites, the excitation spectra are dominated either by 321 or 360 nm band. Turquoise emission of apatites is shifted toward blue region by increasing the excitation wavelength from 231 to 360 nm.
关键词： Silicate apatite,Luminescence,Wet chemical synthesis,Phosphors
更新于2025-09-23 15:22:29