Investigation of the influence of silver and tin on the luminescence of trivalent europium ions in glass

Europium-doped aluminophosphate glasses prepared by the melt-quenching technique have been studied by photoluminescence (PL) and X-ray photoelectron spectroscopy (XPS). The effects of silver and tin doping, and of further thermal processing on Eu³⁺ ions luminescence have been assessed. For the glass system containing only europium, Eu³⁺ PL observed under UV excitation is suggested to occur through energy transfer from the excited glass host. After silver and tin doping, an enhanced UV excited Eu³⁺ PL has been indicated to occur essentially due to radiative energy transfer from isolated Ag⁺ ions and/or two fold-coordinated Sn centers. Since thermal processing of the material leads to a quenching effect on Eu³⁺ PL and Ag nanoparticles (NPs) formation due to reduction of silver ions by tin, XPS was employed in order to investigate the possibility for Eu³⁺→Eu²⁺ reduction during HT as a potential source of the PL decrease. The data points towards Ag NPs as main responsible for the observed weakening of Eu³⁺ PL.     

Improvement of the properties of CSD-processed (Pb0.76Ca0.24)TiO3 thin films by control of the solution chemistry

Ferroelectric (Pb_0.76Ca_0.24)TiO₃ thin films were prepared on platinized Si substrates by chemical solution deposition (CSD). Two different synthetic strategies were adopted to optimize the functionality of the resulting perovskite films: (1) tailoring the schedule of the solution synthesis and (2) chemical selectivity of the calcium precursor. The choice of an appropriate synthetic procedure led to homogeneous sols constituted by a single distribution of particles, as revealed by dynamic light scattering (DLS). Stronger polymeric structures in the sol network are believed to prevent atomic diffusion of metal cations during crystallization at higher temperatures, and perovskite films with a uniform compositional profile and without any detrimental interface with the electrode were measured by Rutherford backscattering spectroscopy (RBS). On the other hand, phase formation and microstructure of crystalline films were strongly affected by the calcium compound used, i.e. calcium acetate or calcium acetylacetonate. The single decomposition mechanism of the last one, with absence of intermediate carbonates, resulted in the prompt crystallization of the perovskite phase (375°C) and an enhanced grain-growth mechanism that led to dense films formed by larger grains. Consequently, the optimized ferroelectric (Pb_0.76Ca_0.24)TiO₃ films showed superior electrical properties: maximum values of dielectric constant nearly doubled and a relative increase in the remanent polarization being ∼40% (P _r =23 μC/cm²). The potential application of these films in functional microelectronic devices is also demonstrated.     

SiOxNy thin films with variable refraction index: Microstructural, chemical and mechanical properties

In this work amorphous silicon oxynitride films with similar composition (ca. Si_0.40N_0.45O_0.10) were deposited by reactive magnetron sputtering from a pure Si target under different N₂-Ar mixtures. Rutherford backscattering (RBS) studies revealed that the coatings presented similar composition but different density. The mechanical properties evaluated by nanoindentation show also a dependence on the deposition conditions that does not correlate with a change in composition. An increase in nitrogen content in the gas phase results in a decrease of hardness and Young's modulus.The microstructural study by high resolution scanning electron microscopy (SEM-FEG) on non-metalized samples allowed the detection of a close porosity in the form of nano-voids (3-15 nm in size), particularly in the coatings prepared under pure N₂ gas. It has been shown how the presence of the close porosity allows tuning the refraction index of the films in a wide range of values without modifying significantly the chemical, thermal and mechanical stability of the film.     

Likelihood analysis of the minimal AMSB model

We perform a likelihood analysis of the minimal anomaly-mediated supersymmetry-breaking (mAMSB) model using constraints from cosmology and accelerator experiments. We find that either a wino-like or a Higgsino-like neutralino LSP, \(\tilde{\chi }^0_{1}\), may provide the cold dark matter (DM), both with similar likelihoods. The upper limit on the DM density from Planck and other experiments enforces \(m_{\tilde{\chi }^0_{1}} \lesssim 3 \,\, \mathrm {TeV}\) after the inclusion of Sommerfeld enhancement in its annihilations. If most of the cold DM density is provided by the \(\tilde{\chi }^0_{1}\), the measured value of the Higgs mass favours a limited range of \(\tan \beta \sim 5\) (and also for \(\tan \beta \sim 45\) if \(\mu > 0\)) but the scalar mass \(m_0\) is poorly constrained. In the wino-LSP case, \(m_{3/2}\) is constrained to about \(900\,\, \mathrm {TeV}\) and \(m_{\tilde{\chi }^0_{1}}\) to \(2.9\pm 0.1\,\, \mathrm {TeV}\), whereas in the Higgsino-LSP case \(m_{3/2}\) has just a lower limit \(\gtrsim 650\,\, \mathrm {TeV}\) (\(\gtrsim 480\,\, \mathrm {TeV}\)) and \(m_{\tilde{\chi }^0_{1}}\) is constrained to \(1.12 ~(1.13) \pm 0.02\,\, \mathrm {TeV}\) in the \(\mu >0\) (\(\mu <0\)) scenario. In neither case can the anomalous magnetic moment of the muon, \((g-2)_\mu \), be improved significantly relative to its Standard Model (SM) value, nor do flavour measurements constrain the model significantly, and there are poor prospects for discovering supersymmetric particles at the LHC, though there are some prospects for direct DM detection. On the other hand, if the \(\tilde{\chi }^0_{1}\) contributes only a fraction of the cold DM density, future LHC Open image in new window -based searches for gluinos, squarks and heavier chargino and neutralino states as well as disappearing track searches in the wino-like LSP region will be relevant, and interference effects enable \(\mathrm{BR}(B_{s, d} \rightarrow \mu ^+\mu ^-)\) to agree with the data better than in the SM in the case of wino-like DM with \(\mu > 0\).     

Role of nuclear motion in double ionization of molecular hydrogen by a single photon

We examine the origin of recently observed variations with internuclear distance (R) of the fully differential cross sections for double ionization of aligned H2 by absorption of a single photon. Using the results of fully converged numerical solutions of the Schr?dinger equation, we show that these variations arise primarily from pronounced differences in the R dependence of the parallel and perpendicular components of the ionization amplitude. We also predict that R dependences should be readily observable in the asymmetry parameter for photodouble ionization, even in experimental measurements that are not differential in the energy sharings between ejected photoelectrons.     

Nanostructures in calcia stabilized hafnia thin films observed by PAC as a function of temperature

The hyperfine quadrupole interaction at Hf sites in films and powders of 14 mol% CaO–HfO₂ and 20 mol% CaO–HfO₂ has been determined as a function of temperature. Results indicate the formation of a cubic solid solution and other microstructures assigned to the ?₁ (CaHf₄O₉) and ?₂ (Ca₆Hf₁₉O₄₄) phases. Dynamical effects on the electric field gradient reveal the existence of oxygen vacancies movements in the solid solution. The thermal behavior of the relaxation constant observed in films allowed the determination of activation energies of 0.54 eV and 0.70 eV for the 14 mol% and 20 mol% CaO doped hafnias, respectively. The influence of the microdomains and the stability of the cubic solid solution are discussed.     

Stoichiometry,Association Constant,and Solvation Model of Chiral Hydroxyfuranones in the Presence of Pirkle's Alcohols

ABSTRACT

(S)-(+)-Dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone, (R)-(-)-dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone, (S)-(-)-dihydro-4-hydroxy-2(3H)-furanone, and (S)-(-)-5-hydroxymethyl-2(5H)-furanone in the presence of pure enantiomers of 2,2,2-trifluoro-1-(9-anthryl)ethanol were studied by ¹H NMR in deuterated chloroform solutions. Experimental Job's plots suggest that the resulting solvates are formed with one molecule of solute and one of the chiral solvating agent. From the magnitude of the association constant determined for (S)-(+)-dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone in the presence of (R)-(-)-2,2,2-trifluoro-1-(9-anthryl)ethanol (1.26 ± 0.09 M^?1), it is inferred that the solvate is weak and cannot be isolated at 298 K. The correlation between the magnitude of induced chemical shifts, NOESY maps, and the known configuration of solutes and chiral solvating agents suggests that intermolecular hydroxyl-hydroxyl interaction is the primary interaction. Accordingly, the secondary interaction might occur between benzylic-hydrogen of the chiral solvating agent and the carbonyl- or furan ring-oxygen atoms of the solute.     

Raman Spectroscopy Analysis of a Playing Card from the 18th Century

We present the characterization, by means of three complementary experimental techniques (optical microscopy [OM], scanning electron microscopy equipped with energy dispersive X-Ray spectroscopy [SEM-EDX], and micro-Raman spectroscopy [µRaman]), of a card belonging to a deck of the Spanish pattern made in Perú at the time of Virreinato de Perú (18th century). The objective is to obtain detailed information on the pictorial palette used for the decoration of the cards, where two basic colors, red and green, are seen. Small samples from both colored regions were analyzed.     

Lanthanide-Sensitized Luminescence as a Promising Tool in Clinical Analysis

Abstract

The recent applications and novelties of lanthanide-sensitized luminescence (LSL) as a detection technique in clinical analysis are here reviewed. In LSL, lanthanide ions form complexes with organic compounds; in these complexes, the energy absorbed by the organic chromophore (usually the analyte) at its characteristic excitation wavelength is transferred to a triplet state of the molecule and then transferred to a resonance level of the lanthanide ion, which finally emits luminescence at its particular emission wavelength. The characteristics of this process will be reviewed and particular attention will be paid to the development of automatic methods of analysis, fluorescence probes, or flow-through optosensors, due to their potential applications in clinical analysis. A critical discussion of the advantages and handicaps of each analytical method is done and the trends of analytical chemistry in this research field are also presented.     

Metal-doped apatitic calcium phosphates: preparation,characterization, and reactivity in the removal of hydrogen sulfide from gas phase

With the expansion of human activities, there are more and more living areas adjacent to industrial and/or agricultural activities such as chemical processes, petroleum processes, paint finishing, food processing, livestock farming, composting plants etc. Bad odor is part of several nuisances caused by industrial and/or agricultural activities. Hydrogen sulfide (H₂S) is a typical odorous molecule which causes foul odor at very low concentration. This molecule is formed in different industrial installations, in particular in coal combustion, and petrochemical refinery. The separation and/or transformation of H₂S from gas phase to odorless products are important processes for sustainable development. In this paper, we communicate the preparation of new sorbents for the sorption of H₂S from a synthetic gas effluent. These sorbents consist in an inorganic phase (hydroxyapatite) as host particles, and well-dispersed particles of a metal oxide as guest particles which are the active phase for the removal of H₂S. At room conditions, iron, lead, and zinc doped calcium phosphates were found to be effective for the removal of H₂S. The performance of the sorbents depends on preparation method and the nature of active phases. This opens new prospects for the treatment of H₂S from gas phase.