Люминесцентные свойства нестехиометрических кристаллов ниобата лития различного состава и генезиса (обзор)

A brief review of the features of the defect structure and studies of the luminescent properties of nonlinear optical lithium niobate crystals of various compositions and genesis was given. It was established that the electron-hole pair NbNb4+-O- in the oxygen-octahedral cluster NbO6 emitted in the short-wavelength region of the visible spectrum (400-500 nm), while point defects (VLi and NbNb4+-NbLi4+ bipolarons) - in the long-wavelength region (500-620 nm). At the ratio of Li/Nb≈1 the luminescence was extinguished in the visible region of the spectrum due to decreasing the intrinsic luminescence centers. It was shown that the presence of polaron luminescence in the near-IR region (700-1050 nm) was due to the small polarons NbLi4+ and impurity ions Cr3+ localized in lithium and niobium octahedra. The energy transfer between the luminescence centers in the visible and near-IR spectral regions was detected. Moreover, luminescence in near-IR regions was dominant. Doping of LiNbO3 crystals with zinc and magnesium at ZnO<4.46 mol.% and MgO<5.29 mol.% led to decreasing luminescence of intrinsic defects (VLi, NbNb4+-NbLi4+). However, there was an increase of the contribution of the short-wave spectrum component at higher dopant concentrations because of the introduction of Zn and Mg into the origin positions of Nb ions.

Near Infrared Fluorescent Nanostructure Design for Organic/Inorganic Hybrid System

Near infrared (NIR) light offers high transparency in biological tissue. Recent advances in NIR fluorophores including organic dyes and lanthanide-doped inorganic nanoparticles have realized the effective use of the NIR optical window for in vivo bioimaging and photodynamic therapy. The narrow energy level intervals used for electronic transition that involves NIR light, however, give rise to a need for guidelines for reducing heat emission in luminescence systems, especially in the development of organic/inorganic hybrid structures. This review presents an approach for employing the polarity and vibrational energy of ions and molecules that surround the luminescence centers for the development of such hybrid nanostructures. Multiphonon relaxation theory, formulated for dealing with heat release in ionic solids, is applied to describe the vibrational energy in organic or molecular systems, referred to as phonon in this review, and we conclude that surrounding the luminescence centers either with ions with low vibrational energy or molecules with small chemical polarity is the key to bright luminescence. NIR photoexcited phosphors and nanostructures in organic/inorganic mixed systems, designed based on the guidelines, for photodynamic therapy are reviewed.

Structure and optic properties of the nanocomposites based on polypropylene and amorphous silica nanoparticles

The structure and optic properties of the transparent PP+SiO2 nanocomposites with a relatively high refractive index and enhanced luminescence properties were investigated. X-ray analysis, Fourier-transform infrared (FTIR), Visible-ultraviolet, and photoluminescence spectroscopic methods were used for investigation. The XRD analysis indicated that the fraction of the amorphous phase of the polycrystalline polymer decreases with the introduction of SiO2 nanoparticles. Even though SiO2 nanoparticle is amorphous itself, they play the role of the crystallinity centers in the polymer matrix, and the degree of crystallinity increases in polymer nanocomposites. According to UV-vis spectroscopic analysis that, with the increasing of the concentration of SiO2 nanoparticles distributed in the polymer matrix, the absorption intensity of the samples also increases. It was explained by the hyperchromic effect which is related to raising the optical density of the polymer by introducing the filler particles (SiO2). It was calculated bandgap energy and refractive index on the base of the UV spectra of samples. It has been found that at low concentrations of amorphous silica nanoparticles, the polymer nanocomposite retains its transparency despite having a relatively high refractive index (1.96). Furthermore, the photoluminescence (PL) spectrum of nanocomposites was investigated depending on filler concentration. It was clear that the intensity of the PL spectrums increases with the increase of the filler concentration that is explained by the raising of the luminescence centers in the nanocomposite material. These luminescence centers are oxygen-deficit centers in the spatial structure of the amorphous silica nanoparticles.

Broadband near-infrared persistent luminescence in Ni2+-doped transparent glass-ceramic ZnGa2O4

Transparent glass-ceramic is a highly attractive class of materials for photonic application. Transition metal ions are promising candidates for luminescence centers thanks to the sensitivity to the ligand ions of...

Achievement of narrow-band blue-emitting phosphors KScSr1−yCaySi2O7:Bi3+ by the migration of luminescence centers

Narrow-band blue emitting phosphor KScSr1−yCaySi2O7:0.07Bi3+ with FWHM 40 nm.