Preparation of neodymium-doped yttrium aluminum garnet powders and fibers

Using nitrate precursors, a novel spray-drying assisted citrate gel process for the preparation of neodymium-doped yttrium alumi- num garnet （YAG） phase was developed. Synthesis of single-phase polycrystalline YAG was achieved at temperatures as low as 800 ℃ using the spray-drying methodology whilst conventional approaches currently available require 1000 ℃. Initially, a solution was prepared by mixing aluminum and yttrium nitrates, citric acid, etilenglycol and neodymium oxide. This solution was dried by pulverization （spray dryer） to obtain aggregated precursor powders of the compound. These aggregates were calcined at 800, 850 and 900 ℃ to determine the phase evolution from amorphous to crystalline by X-ray diffraction （XRD）. The morphology of aggregates was characterized by scanning electron microscopy （SEM） and transmission electron microscopy （TEM）. Moreover, through XRD it was determined that the crystallization of YAG phase started at about 800 ℃ without any intermediate phases. The powders were composed of spherical aggregates with an average diameter of 1 um. From these powders, ceramic fibers with additions of 2at.% and 5at.% Nd, were extracted from the melt with diameters ranging from 30 um to 50 um.     

Work function of yttrium and lanthanide single crystals

In this paper experimental and calculated data available in the literature on the work function of yttrium and lanthanide single crystals has been organized. Data according to the anisotropy of the different faces and types of crystal lattices has been classified.Institute of Problems in Materials Science, Academy of Sciences of the Ukraine, Kiev. Translated from Poroshkovaya Metallurgiya, Nos. 1–2, pp. 92–97, January–February, 1994.     

Controlled synthesis and formation mechanism of sodium yttrium fluoride nanotube arrays

Cubic and hexagonal sodium yttrium fluoride were successfully synthesized from yttrium nitrate, sodium fluoride and poly-ethanediol in propanetriol solvent under a facile hydrothermal route. By regulating the molar ratio of yttrium and fluoride, hydrothermal tem-perature and reaction time, the phase and shape of sodium yttrium fluoride were commendably controlled. The as-prepared products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectrum (EDS) techniques. It was revealed that the hollow-structured Na(Y1.5Na0.5)F6 nanotubes self-assembled and arrayed orientedly to be bamboo raft-shaped. The for-mation of hexagonal Na(Y1.5Na0.5)F6 nanotube arrays was attributed to solid-liquid-solid process and Oswald ripening. This study provided a simple method to prepare hexagonal bamboo raft-shaped Na(Y1.5Na0.5)F6 on a large scale, which broadened their practical applications.     

Synthesis and characterization of branched yttrium hydroxide fluoride microcrystals with hierarchical tubular structure

Hexagonal yttrium hydroxide fluoride microcrystals were prepared by a two-step hydrothermal route using yttrium nitrate, sodium hydroxide and sodium fluoride as raw materials to react in propanetriol solvent. The samples were characterized by powder X-ray diffraction (XRD), energy dispersive spectrum (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier trans-form infrared spectroscopy (FT-IR), thermogravimetre and differential-thermogravimetric analysis (TG-DTA), which revealed that Y(OH)2.14F0.86 microcrystals were multi-branched and that the branches of Y(OH)2.14F0.86 microcrystals were composed of hierarchical tubes. This novel multi-branched and intriguing hierarchical tubular structure of yttrium hydroxide fluoride maybe has a potential application in photoelectric crystals. The formation of branched Y(OH)2.14F0.86 microcrystals with hierarchical tubular structure were due to the substitution reaction and Oswald ripening.     

Fast growth of cerium-doped lutetium yttrium orthosilicate single crystals and their scintillation properties

The growth of high-quality and large-size cerium-doped lutetium yttrium orthosilicate (Ce:(LuY)₂SiO₅, Ce:LYSO) crystals with lower cost has great influence on their applications in various physical devices. According to the chemical bonding theory of single crystal growth, the fast thermodynamic growth direction of Ce:LYSO is [010] direction. In this work, the maximum pulling rate of 3.5 mm/h is obtained along [010] direction of Ce:LYSO via the Czochralski (Cz) method. Finally, Ce:LYSO bulk single crystals with diameter of 64 mm and length of 220 mm and mass of 4.2 kg are grown. The luminescence performance of low-doped Ce:LYSO for nuclear irradiation (²²Na) detector device was studied. Light yield of 26193 ph/MeV and decay time of 38 ns are obtained. The present work provides a promising fast growth approach to achieving large size functional bulk crystal via both thermodynamic and kinetic controls.