High-Entropy Layered Rare Earth Hydroxides.

New high-entropy layered rare earth hydroxides ─ (Y,Eu,Gd,Er,Sm)2(OH)5NO3, (Y,Eu,Gd,Er,Tb)2(OH)5NO3, (Y,Eu,Gd,Er,Yb)2(OH)5NO3, (Y,Eu,Gd,Er,Nd)2(OH)5NO3, and (Y,Eu,Gd,Er,Nd,Sm,Tb)2(OH)5NO3 ─ were obtained using a hydrothermal microwave method. The annealing of layered rare earth hydroxides at 900 °C resulted in the corresponding high-entropy rare earth oxides. Based on inductively coupled plasma atomic emission spectroscopy data, the values for configurational entropy for both rare earth hydroxides and oxides were estimated, confirming the formation of high-entropy compounds. Energy-dispersive X-ray spectroscopy mapping, including mapping in the scanning transmission microscopy mode, showed no signs of chemical segregation and confirmed uniform rare earth elements' distribution both in the particles of high-entropy layered basic nitrates and in the particles of high-entropy oxides. The ratios of rare earth cations in the initial aqueous solutions of mixed nitrates were close to the ratios of cations in the resulting high-entropy layered rare earth basic nitrates and high-entropy rare earth oxides.

Synthesis of SrF2:Yb:Er ceramic precursor powder by co-precipitation from aqueous solution with different fluorinating media: NaF, KF and NH4F.

The major challenge in optical ceramic technology is the quality of the starting precursor powder for pressing, which is a key element in the optical ceramic industry. One express and helpful technique for the estimation of powder quality is the estimation of the quantum yield of up-conversion luminescence; therefore precursor powders must exhibit high values of up-conversion luminescence efficiency. Single-phase solid solutions based on strontium fluoride doped with ytterbium and erbium were synthesised by co-precipitation from aqueous solutions using sodium fluoride, potassium fluoride and ammonium fluoride as fluorinating agents. The asymmetry of X-ray diffraction maxima indicated the presence of two populations of particles with the same chemical composition. The processes of extended flat particles' growth from smaller particles with a spherical morphology were revealed with transmission electron microscopy and X-ray diffraction. It was shown that when sodium fluoride and potassium fluoride were used they entered the crystal structure in an amount of 3-4 mol% and 1 mol%, respectively. The introduction of sodium and potassium led to an improvement in the sintering ability of particles and a significant increase in the particle size in ceramics by a factor of 5 and 2, respectively, in comparison with the use of ammonium fluoride. The quantum yield values of up-conversion luminescence at the level of tenths of a percent at a low pump power density of 0.1 W cm-2 were very high, which suggests that these synthetic techniques can be considered to be promising for the preparation of precursors of laser ceramics.

The first amorphous and crystalline yttrium lactate: synthesis and structural features.

The synthesis and crystal structure of the first molecular yttrium lactate complex, Y(Lac)3(H2O)2, is reported, where the coordination sphere of yttrium is saturated with lactate ligands and water molecules, resulting in a neutral moiety. In Y(Lac)3(H2O)2, hydrogen bonding between α-hydroxy groups and water molecules allows for the formation of 2D layers. A subtle variation in synthetic conditions, i.e. a slight increase in pH (5.5 instead of 4.5) promoted the formation of a semi-amorphous fibrous material with a presumed chemical composition of Y4(OH)5(C3H5O3)7·6H2O. The flattened fibres in this material are responsible for its good flexibility and foldability.

Combined SANS and SAXS study of the action of ultrasound on the structure of amorphous zirconia gels.

In the present work, we have studied for the first time the combined effect of both sonication and precipitation pH on the structure of amorphous zirconia gels synthesized from zirconium(IV) propoxide. The techniques of small-angle neutron and X-ray scattering (SANS and SAXS) and low temperature nitrogen adsorption provided the integral data on the changes in the microstructure and mesostructure of these materials caused by ultrasonic (US) treatment. Amorphous ZrO2·xH2O synthesized under ultrasonic treatment was found to possess a very structured surface, characterized by the surface fractal dimension 2.9-3.0, compared to 2.3-2.5 for the non US-assisted synthesis, and it was also found to possess a higher specific surface area, while the sizes of the primary particles remain unchanged.