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)
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>
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>1Ì… 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