2 research outputs found

    Synthesis and Characterization of the New Strontium Borogermanate Sr<sub>3–<i>x</i>/2</sub>B<sub>2–<i>x</i></sub>Ge<sub>4+<i>x</i></sub>O<sub>14</sub> (<i>x</i> = 0.32)

    No full text
    The strontium borogermanate Sr<sub>3–<i>x</i>/2</sub>B<sub>2–<i>x</i></sub>Ge<sub>4+<i>x</i></sub>O<sub>14</sub> (<i>x</i> = 0.32) was synthesized by high-temperature solid-state reaction of SrO, GeO<sub>2</sub>, and H<sub>3</sub>BO<sub>3</sub> in a NaF/KF flux system using platinum crucibles. The structure determination revealed that Sr<sub>3–<i>x</i>/2</sub>B<sub>2–<i>x</i></sub>Ge<sub>4+<i>x</i></sub>O<sub>14</sub> (<i>x</i> = 0.32) crystallizes in the trigonal space group <i>P</i>321 (No. 150) with the parameters <i>a</i> = 800.7(2) and <i>c</i> = 488.8(2) pm, with <i>R</i>1 = 0.0281, <i>wR</i>2 = 0.0671 (all data), and <i>Z</i> = 1. The crystal structure of Sr<sub>3–<i>x</i>/2</sub>B<sub>2–<i>x</i></sub>Ge<sub>4+<i>x</i></sub>O<sub>14</sub> (<i>x</i> = 0.32) consists of distorted SrO<sub>8</sub> cubes, GeO<sub>6</sub> octahedra, GeO<sub>4</sub> tetrahedra, and BO<sub>4</sub> tetrahedra. In addition to the structural investigations, Raman and IR spectroscopic investigations were carried out

    Structural Redetermination and Photoluminescence Properties of the Niobium Oxyphosphate (NbO)<sub>2</sub>P<sub>4</sub>O<sub>13</sub>

    No full text
    The structure of (NbO)<sub>2</sub>P<sub>4</sub>O<sub>13</sub> was solved and refined based on new single-crystal diffraction data revealing considerably more complexity than previously described. (NbO)<sub>2</sub>P<sub>4</sub>O<sub>13</sub> crystallizes in the triclinic space group <i>P</i>1̅ with <i>Z</i> = 6. The lattice parameters determined at room temperature are <i>a</i> = 1066.42(4) pm, <i>b</i> = 1083.09(4) pm, <i>c</i> = 1560.46(5) pm, α = 98.55(1)°, β = 95.57(1)°, γ = 102.92(1)°, and <i>V</i> = 1.7213(2) nm<sup>3</sup>. The superstructure contains 64 unique atoms including two disordered semioccupied oxygen positions. An unusual 180° bond angle between two [P<sub>4</sub>O<sub>13</sub>]<sup>6–</sup> groups was refined to form half-occupied, split positions in agreement with previous reports. The IR and Raman spectra reflect the appearance of overlapping bands assignable to specific group vibrations as well as P–O–P linkages present in the [P<sub>4</sub>O<sub>13</sub>]<sup>6–</sup> entities. Investigation of the powdered product concerning its photoluminescence properties revealed an excitability in the UV at 270 nm assigned to O2p–Nb4d charge transfer transitions. A resulting broad-band emission with the maximum in the visible region at 455 nm was determined
    corecore