Люминесцентный хемосенсор для детектирования паров диметиламина и аммиака

The interaction of tris-dibenzoylmethanate Eu(III) with dimethylamine and ammonia vapors was investigated. It was found that when vapors of aqueous solutions of analytes are exposed to tris-dibenzoylmethanate Eu(III) impregnated into the SiO2 matrix, an optical response is observed in the form of an increase in the luminescence intensity of Eu(III). Changes in the luminescence spectra and luminescence excitation of this sensor are analyzed, both under the quenching action of water vapor and under the sensitizing action of analyte vapors. The main points recorded in the excitation spectra are noted, which are important for understanding the processes occurring in the near environment of the lanthanide center. The luminescent chemosensor is promising for creating sensors for detecting ammonia and amines in food safety control and environmental monitoring. Shishov A.S., Mirochnik A.G.

Cubic versus Hexagonal – Phase, Size and Morphology Effects on the Photoluminescence Quantum Yield of NaGdF4:Er3+/Yb3+ Upconverting Nanoparticles

Upconverting nanoparticles (UCNPs) are well-known for their capacity to convert near-infrared light into UV/visible light, benefitting various applications where light triggering is required. At the nanoscale, loss of luminescence intensity...

Novel Amphiphilic Polyfluorene-Graft-(Polymethacrylic Acid) Brushes: Synthesis, Conformation, and Self-Assembly

Novel polyfluorene polymer brushes with polymethacrylic acid side chains were obtained by atom transfer radical polymerization (ATRP) and activator generated by electron transfer (AGET) ATRP of tert-butyl methacrylate on polyfluorene multifunctional macroinitiator, followed by protonolysis of the tert-butyl groups of the side chains. Kinetics of polymerization and molecular weights were fully characterized. These polymer brushes luminesce in the blue region of the spectrum with high quantum yields (0.64–0.77). It was shown that the luminescence intensity of polymer brushes is higher than the luminescence intensity of the macroinitiator (0.61). Moreover, due to their amphiphilic nature, they can form unimolecular micelles when an alcohol solution of the polymer brush is injected into water. These properties can potentially be used in drug delivery and bioimaging.

Improved passivation depth of porous fluorescent 6H-SiC with Si/C faces using atomic layer deposition

We investigated the effects of different growth facets of 6H-SiC and different voltage waveforms on the porous structure and luminescence properties. The structure formed on the surface after anodic etching significantly changed because of the difference in the growth plane, whereas dendritic and columnar pores were observed inside the Si- and C-face samples. These large porous structures were shown to promote the penetration depth of the atomic-layer-deposited Al2O3 films, and a recorded passivation depth of 30-µm layer was confirmed in C-face porous SiC. From the results using fluorescence microscope and PL spectra measurement, it was concluded that the pulsed-voltage etching was preferable for fabricating uniform porous structures compared with the constant-voltage etching. However, the enhancement of the luminescence intensity needs to be further improved to realize high luminescent efficiency in porous fluorescent SiC.

SiO2 Coated Up-Conversion Nanomaterial Doped with Ag Nanoparticles for Micro-CT Imaging

In this study, a new method for synthesizing Ag-NaYF4:Yb3+/Er3+ @ SiO2 nanocomposites was introduced. Using a hydrothermal method, the synthesized Yb3+- and Er3+-codoped NaYF4 up-conversion luminescent materials and Ag nanoparticles were doped into up-conversion nanomaterials and coated with SiO2 up-conversion nanomaterials. This material is known as Ag-UCNPs@SiO2, it improves both the luminous intensity because of the doped Ag nanoparticles and has low cytotoxicity because of the SiO2 coating. The morphology of UCNPs was observed using scanning electron microscopy (SEM), and the mapping confirmed the successful doping of Ag nanoparticles. Successful coating of SiO2 was confirmed using transmission electron microscopy (TEM). Fluorescence spectra were used to compare changes in luminescence intensity before and after doping Ag nanoparticles. The reason for the increase in luminescence intensity after doping with Ag nanoparticles was simulated using first-principles calculations. The cytotoxicity of Ag-UCNPs@SiO2 was tested via the cell counting kit-8 (CCK-8) method, and its imaging ability was characterized using the micro-CT method.

SiO2 Coated Up-conversion Nanomaterial Doped with Ag Nanoparticles for Micro-CT Imaging

In this study, a new method for synthesizing Ag-NaYF4:Yb3+/Er3+ @ SiO2 nanocomposites was introduced. Using a hydrothermal method, the synthesized Yb3+- and Er3+-codoped NaYF4 upconversion luminescent materials and Ag nanoparticles were doped into upconversion nanomaterials and coated with SiO2 up-conversion nanomaterials. This material is known as Ag-UCNPs-SiO2’ it improves both the luminous intensity because of the doped Ag nanoparticles and has low cytotoxicity because of the SiO2 coating. The morphology of UCNPs was observed using scanning electron microscopy (SEM), and the mapping confirmed the successful doping of Ag nanoparticles. Successful coating of SiO2 was confirmed using transmission electron microscopy (TEM). Fluorescence spectra were used to compare changes in luminescence intensity before and after doping Ag nanoparticles. The reason for the increase in luminescence intensity after doping with Ag nanoparticles was simulated using first-principles calculations. The cytotoxicity of Ag-UCNPs-SiO2 was tested via the cell counting kit-8 (CCK-8) method, and its imaging ability was characterized using the micro-CT method.

Using silver nanoparticles for the increase of YAG: Ce luminescence

In this study, silver nanoparticles with an average diameter of 50-70 nm were synthesized by the chemical reduction method. Subsequently, nanoparticles in different concentrations were introduced into the YAG: Ce luminescent powder synthesized by the method of two-stage coprecipitation into hexamine. The luminescence of samples with different contents of nanosilver was investigated. It was shown that the direct addition of nanosilver to YAG: Ce significantly impairs luminescence. Upon calcination at 900 °C, an increase in the luminescence of the YAG: Ce samples with silver nanoparticles was observed; however, the luminescence intensity was lower than that of the reference sample (without nanosilver). After calcination in an inert atmosphere at a temperature of 1550 °C, a significant increase in the luminescence intensity (of the order of 30-40 %) of the samples with the addition of a nanosilver was observed in comparison with the reference sample. Thus, silver nanoparticles can be successfully used to improve the YAG: Ce phosphors.