Alexandr Vladimirovich Popov

A hydrothermal technique with microwave heating (200 °C, 2 hours, 2 magnetrons, 2.45 GHz) was modified to obtain UV-C luminescent LaPO4: Pr3+ colloidal nanorods for the potential use in X-ray cancer theranostics. For further possible biofunctionalization, a compound of tartaric acid formed under basic conditions was used as a coating and stabilizing agent to provide colloidal properties to the surface of nanoparticles in basic to neutral aqueous media, which was confirmed by zeta potential measurements. In addition, the colloidal properties and clustering processes of synthesized LaPO4:Pr3+ nanorods in aqueous solutions with different pH values were studied in real time using a highly sensitive laser ultramicroscope operating according to the “light-sheet” scheme. A comparative analysis of the transmission electron microscopy, X-ray powder diffraction and high-energy spectroscopy showed the different effects of synthesis parameters on the morphological, crystalline and luminescent properties of the obtained nanorods. Through optimization of the synthesis parameters, stable aqueous solutions of m-LaPO4:Pr3+ nanorods with sizes less than 30 nm and an intensity of UV-C luminescence equal to 5-10% of the unmodified nanofibers were obtained.

In the present work, we investigated the effect of light conversion using europium (Eu(III))-based photoconversion covers on the cultivation of agricultural plants and their resistance to stress conditions. Two types of europium nanoparticles were used. The first one was obtained from europium oxide (Eu₂O₃) by laser fragmentation. The second one was Eu³⁺:LaF₃ nanocrystals obtained by hydrothermal-microwave treatment, the content of europium ions in which was 50% of the total amount of cations. Tomatoes (Solanum lycopersicum) and cucumbers (Cucumis sativus) were used as model plants. It was shown that plants grown under cover with Eu₂O₃ (PCC-Eu₂O₃) were 30–40% larger, gave a higher yield, and the activation of gas exchange processes and the light phase of photosynthesis in the leaves in response to the lighting was faster. On the contrary, plants grown under cover with Eu³⁺:LaF₃ (PCC-Eu³⁺:LaF₃) tended to slow down the rate of biomass accumulation and decrease the rate of gas exchange activation. It was shown that photoconversion covers change the resistance of plants to stress conditions: if plants grown under PCC-Eu₂O₃ became more sensitive to heat (+40 °C) and cold (+4 °C) treatment, then plants grown under PCC-Eu³⁺:LaF₃ became more resistant to high and low temperatures. It was found that PCC-Eu₂O₃ inhibited the development of the phytopathogen Phytophthora infestans on tomato plants. It was assumed that changes in the illumination spectrum by the photoconversion covers cause both the activation of plant growth in the case of Eu₂O₃ and an increase in plant resistance in the case of Eu³⁺:LaF₃ applications.

An original method was proposed to reduce the quenching of the NIR fluorescence of colloidal solutions of 0.1 at. % Nd³⁺: LaF₃ nanoparticles (NPs) synthesized by aqueous co-precipitation method followed by hydrothermal microwave treatment. For this, an aqueous colloidal solution of NPs was precipitated by centrifugation and dissolved in the same volume of DMSO. The kinetics of static fluorescence quenching of Nd³⁺ donors of doped NPs dispersed in two solvents was analyzed to determine and to compare the concentrations of OH- quenching acceptors uniformly distributed throughout the volume of the NPs. The dependences of the relative fluorescence quantum yield φ of colloidal solutions on the concentration of OH- groups in the NPs were calculated and were also used to determine concentration of acceptors in the volume of NPs in different solvents. It was found that the concentration of OH- groups in NPs dispersed in DMSO is almost two times lower than in NPs dispersed in water. This gives an almost two-fold increase in the relative fluorescence quantum yield φ for the former. The sizes of synthesized NPs were monitored by common TEM and by applying a rapid procedure based on optical visualization of the trajectories of the Brownian motion of NPs in solution using a laser ultramicroscope. The use of two different methods made it possible to obtain more detailed information about the studied NPs.

Two series of stable aqueous colloidal solutions of Nd³⁺: LaF₃ single-phase well-crystallized nanoparticles (NPs), possessing a fluorcerite structure with different activator concentrations in each series, were synthesized. A hydrothermal method involving microwave-assisted heating (HTMW) in two Berghof speedwave devices equipped with one magnetron (type I) or two magnetrons (type II) was used. The average sizes of NPs are 15.4 ± 6 nm (type I) and 21 ± 7 nm (type II). Both types of NPs have a size distribution that is well described by a double Gaussian function. The fluorescence kinetics of the ⁴F_3/2 level of the Nd³⁺ ion for NPs of both types, in contrast to a similar bulk crystal, demonstrates a luminescence quenching associated not only with Nd–Nd self-quenching, but also with an additional Nd–OH quenching. A method has been developed for determining the spontaneous radiative lifetime of the excited state of a dopant ion, with the significant contribution of the luminescence quenching caused by the presence of the impurity OH– acceptors located in the bulk of NPs. The relative quantum yield of fluorescence and the fluorescence brightness of an aqueous colloidal solution of type II NPs with an optimal concentration of Nd³⁺ are only 2.5 times lower than those of analogous Nd³⁺: LaF₃ single crystals.

Structural and spectroscopic methods are used to study the epitaxial layers of n-type Al xGa1 − xAs solid solutions produced by the metal-organic chemical vapor deposition method. It is shown that,...