The Synthesis, Structure, and Luminescent Properties of TmMgBO Crystals.

TmMgBO spontaneous crystals were synthesized via the flux-growth technique from a KMoO-based solvent. The crystal structure of the compound was solved and refined within the space group 2/. The first principles calculations of the electronic structure reveal that TmMg-pentaborate with an ideal not defected crystal structure is an insulator with an indirect energy band gap of approximately 6.

Synthesis, structure and properties of layered PrMoO-based oxymolybdates doped with Mg.

Undoped and Mg-doped PrMoO oxymolybdate polycrystals and single crystals have been prepared by solid-state reactions and flux growth. The compounds have been characterized by powder X-ray diffraction, energy-dispersive spectroscopy, inductively coupled plasma mass spectrometry, scanning transmission electron microscopy, single crystal X-ray structure analysis, differential scanning calorimetry and thermogravimetry. The (MgO)(PrO)(MoO) (x + y + z = 1) solid solution series has been shown to extend to x = 0.

Characteristic features of polytypism in compounds with the LaWO-type structure.

Crystals with the LaWO-type structure (6H and 5H polytypes) were obtained by a self-flux method from high-temperature solutions. Some of the crystal samples were studied by single-crystal X-ray structure analysis. The diffraction patterns indicated that two phases co-exist in each sample.

Structure of fluorite-like compound based on Nd₅Mo₃O₁₆ with lead partly substituting for neodymium.

A single crystal of Nd5Mo3O16 with lead partly substituting for neodymium, which has a fluorite-like structure, was studied by precision X-ray diffraction, high-resolution transmission microscopy and EDX microanalysis. The crystal structure is determined in the space group Pn3¯n. It was found that the Pb atoms substitute in part for Nd atoms in the structure and are located in the vicinity of Nd2 positions.

X-ray diffraction study of oxygen-conducting compounds Ln₂Mo₂O₉ (Ln = La, Pr).

The La2Mo2O9 (LM) and Pr2Mo2O9 (PM) single crystals are studied using precision X-ray diffraction and high-resolution transmission microscopy at room temperature. The crystal structures are determined in the space group P2(1)3. La and Pr atoms, as well as Mo1 and O1 atoms, are located in the vicinity of the threefold axes rather than on the axes as in the high-temperature cubic phase.