The use of small angle X-ray scattering (SAXS) for the characterisation of lustre surfaces in Renaissance majolica

In this work some Renaissance lustre decorated ceramics have been examined. Our attention was directed to lustre which is a thin decorative metallic film applied on the surfaces of previously glazed ancient pottery.Some 16th century lustre ceramics shards from Deruta, Umbria (Italy) have been analysed by small angle X-ray scattering (SAXS) in order to characterise the dimension of the metal nanocrystals forming the thin lustre layer. This technique appeared to be a powerful tool to characterise lustre films nanostructure and may be successfully used for this purpose together with transmission electron microscopy (TEM). Furthermore, SAXS measurements are extremely suitable for the determination of polydispersity and average interparticle distance.The lustre surfaces have been also analysed by scanning electron microscopy plus X-ray energy dispersive spectrometry (SEM–EDX) in order to identify the metals present (silver, copper or both of them) and to establish copper/silver ratios. From the comparison between SAXS results and compositional data, it was possible to conclude that copper particles are smaller than the silver ones. We have evidenced how the microtexture as well as the chemical composition of the lustre layers are responsible for the gold or red colour typical of the lustre films.     

Luminescence property of Ce-doped silica decorated with S and Cl anions

Ce³⁺-doped silica was synthesized by sol-gel technique and was further decorated with S²⁻ and Cl⁻ anions through chemical exchange in controlled ambient at elevated temperature. The structure and optical property of samples were examined by X-ray diffraction spectrum, XPS pattern, reflection pattern, and photoluminescence patterns. There is a broad luminescence band at 445 nm under the excitation at 320 nm in the Ce³⁺-doped silica heat-treated in air at 1000 °C. The heat-treatment of the sample in vacuum at 800 °C can increase the intensity of luminescence but have no effect on the wavelength of luminescence. The decoration of S²⁻ and Cl⁻ anions cannot only increase the luminescent intensity but also shift the luminescent wavelength to shorter wavelength.     

Luminescence properties of humic substances

A detailed analysis of luminescence properties of humic substances and fulvic acids extracted from peat soil is carried out for the first time. Their fluorescence excitation and emission spectra, fluorescence lifetimes, phosphorescence excitation and emission spectra, and phosphorescence lifetimes at room temperature are investigated. The nature of chromophores of humic substances is discussed. Presented at the International Symposium on Peat Organic Substances, May 15–19, 1995, Minsk, Belarus. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 64, No. 4, pp. 489–493, July–August, 1997.     

Luminescence properties of calcium-iodide crystals

The effect of the conditions of preparation, temperature, and the action of x rays on the luminescence properties of calcium-iodide scintillation crystals is investigated. On the basis of the results of a study of the spectral characteristics of CaI₂ and CaI₂:H₂ crystals for optical and x-ray excitation in the temperature range 90–400 K, also taking into account the results of a study of the luminescence properties of CaI₂ crystals activated by Cl⁻, Br⁻, OH⁻, and Ca²⁺ impurities, it is suggested that the 236-nm band observed in the excitation spectra of crystals of calcium iodide may be caused by an uncontrollable hydrogen impurity. The luminescence of these crystals with maximum at 395 nm is ascribed to radiative recombination of excitons trapped at H⁻ ions. Zh. Tekh. Fiz. 69, 135–136 (January 1999)     

Luminescence properties of highly purified acetophenone

Acetophenone is found to exhibit no prompt fluorescence at the 10^?6 quantum yield level when purified by fractional distillation and a double GC preparation. The emission observed is primarily room temperature, solution phosphorescence and the solvent blank. A classical analysis of 77 K phosphorescence data supports and n→π¹ triplet assignment with polar solvents and a π→π¹ assignment with very non-polar solvents.     

Luminescence properties of Tb implanted ZnO

ZnO [0 0 0 1] crystals were irradiated at room temperature with Tb⁺ ions of 400 keV with fluences from 1×10¹⁶ to 2×10¹⁷ cm⁻². The implanted layer was examined by several methods, including radioluminescence (RL), Rutherford backscattering spectrometry (RBS) and optical spectroscopy. The optical extinction spectra were simulated using Mie scattering theory. Absorption spectra predicted by Mie theory for particles of decreasing diameter were compared with those obtained experimentally. Some qualitative agreement between theoretical and experimental data was achieved. It was also shown that the intensities of the characteristic green emission bands associated with Tb produced by ⁵D₄→⁷F_j=5,4 transitions have increased about 8 times after annealing. Optical spectroscopy and radioluminescence data have revealed that the ion implantation is a promising tool for synthesizing Tb nanoparticles in the ZnO surface. The Tb nanoparticles exhibit a rather weak plasma resonance.     

Surface elastic properties of Si decorated with Ni nanostructures

Brillouin spectroscopy was used to study elastic properties of the Si (1 1 1) decorated with Ni nanostructures deposited by nanospherical lithography. The height of the nickel nanostructure deposited was about 25 nm, while the area taken by the structure differed depending on the type of matrix used. It was found that the Ni nanostructures change the velocity of both bulk and surface phonons in the systems studied. This finding is in contradiction to the results concerning the surface phonons velocities in different media covered with a homogenous thin metal film, in which the effect was observed for films thicker than 70 nm.     

Cu掺杂无水芒硝的光致发光特性

在气温1 100℃下,将纯天然无水芒硝(Na2SO4)和Cu的混合粉末加热20 min,制备了Na2SO4:Cu发光材料.在室温中测量了光致发光谱.通过实验结果发现发射光谱形状依赖于激发波长,在260nm激发下的发射光谱是由峰值位于430 nm处的宽带谱构成,所得到的宽带谱归属于Cu+内电子的3d94s→3d10跃迁....     

Luminescence properties of divinylbenzene and methylmethacrylate copolymers

This article describes our attempts to produce ”nonexcimer” polymer systems by means of rigid fixation of chromophore groups positioned between two vinyl bonds. Divinylbenzene and methylmethacrylate copolymers were chosen as such systems. Study of the optical properties of synthesized copolymers showed their constancy in a wide region of specific concentrations of chromophore groups. The absence of luminescent properties modification in a wide concentrations range proves the possibility of eliminating the intrasystem energy traps by means of rigid fixation of chromophores in polymer.     

Luminescence properties of Eu ion-exchanged Y-type zeolite

The luminescent properties of Eu ion incorporated in a Y-type zeolite have been studied. The emission spectrum at room temperature is due to the transition between ⁵D and ⁷F levels of the Eu³⁺ ion. However the emission band for Eu³⁺ decreased as this compound was degassed at above 300°C and the band emission, peaked at 445 nm, appeared. This band emission is associated with Eu²⁺ 5d to 4f transition.     

Magnetic properties and quantum entanglement on decorated zigzag ladder

Magnetic properties and quantum entanglement of Heisenberg model with two-, three- and four-site exchange interactions on zigzag ladder are studied. Magnetic properties and concurrence (measure of quantum entanglement) are analyzed by means of variational mean-field-like treatment based on the Gibbs-Bogoliubov inequality. The magnetization plateau and second-order phase transition are obtained. A comparison of the entanglement and magnetic characteristics for the zigzag ladder is made. Our calculations show that in the antiferromagnetic region the behavior of the concurrence coincides with that of the magnetization.     

Magnetotransport properties of graphene layers decorated with colloid quantum dots

The hybrid graphene-quantum dot devices can potentially be used to tailor the electronic, optical, and chemical properties of graphene. Here, the low temperature electronic transport properties of bilayer graphene decorated with PbS colloid quantum dots(CQDs) have been investigated in the weak or strong magnetic fields. The presence of the CQDs introduces additional scattering potentials that alter the magnetotransport properties of the graphene layers, leading to the observation of a new set of magnetoconductance oscillations near zero magnetic field as well as the high-field quantum Hall regime.The results bring about a new strategy for exploring the quantum interference effects in two-dimensional materials which are sensitive to the surrounding electrostatic environment, and open up a new gateway for exploring the graphene sensing with quantum interference effects.     

Luminescence and photoconductivity properties of porous polycrystalline silicon

In recent years, the photoluminescence and the photoconductivity of porous silicon were comprehensively studied. But the photoluminescence and the photoconductivity of porous polycrystalline silicon have not been wholely studied. In this paper, the results showed that luminescent property of the samples prepared by poly-crystal silicon wafers may be related to the defects on Si complexes surface, which can be proved by microwave-detected photoconductivity decay measurements. Furthermore, the luminescence of samples was disappeared under the external illumination, which may be related to the elimination of luminescent-centers. In addition, the conductivities of the samples were dependent on etched time and current density, and the large porosity of samples led to isotropic photoconductivity, which may be related to the change of energy band structure of the devices.     

Luminescence properties of oxide coatings on aluminum alloys

This is a study of the luminescence properties of coatings formed on aluminum alloys by anodizing in electrolytic solutions based on oxalic, sulfuric, and tartaric-sulfonic acids. At least two emission centers, with band maxima in the ranges of 390–410 and 470–510 nm, can be reliably identified in the photoluminescence spectra. The first type of center is characterized by single-band photoluminescence excitation spectra and the second, by two-band spectra. An analysis of the two-band photoluminescence excitation (PLE) spectra in the range of 470–510 nm shows that the position of the narrow short-wavelength PLE spectrum near 272 nm is independent of the type of acid used in the anodization process. The position and shape of the other PLE spectral bands depend both on the type of acid used and on the processing of the alloy or alumina surfaces. It is assumed that defect-free alumina centers are responsible for the 272 nm PLE band, while the other photoluminescence bands are caused primarily by different divacancies of oxygen (F₂⁺ {F_2^+} , F ₂, and F₂⁺² {F_2^{+2}} centers) whose origin is governed by the type of electrolyte.     

Luminescence properties of Tb-activated yttrium gallium garnet phosphors

Comparison of luminescence properties between electron-excited and uv-excited yttrium gallium garnet: Tb phosphors is reported. Although the thermoluminescence and phosphorescence in both cases are quite alike once traps are filled, an apparent difference in the behavior of trap filling has been observed. Small addition of V₂O₃ to these phosphors revealed a unique effect on luminescence properties either with the electron excitation or with the uv excitation.