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Crystal structure refinement of magnesium zinc divanadate, MgZnV(2)O(7), from powder X-ray diffraction data
The crystal structure of magnesium zinc divanadate, MgZnV(2)O(7), was determined and refined from laboratory X-ray powder diffraction data. The title compound was synthesized by a solid-state reaction at 1023 K in air. The crystal structure is isotypic with Mn(0.6)Zn(1.4)V(2)O(7) (C2/m; Z = 6) and i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183434/ https://www.ncbi.nlm.nih.gov/pubmed/34164132 http://dx.doi.org/10.1107/S2056989021004503 |
Sumario: | The crystal structure of magnesium zinc divanadate, MgZnV(2)O(7), was determined and refined from laboratory X-ray powder diffraction data. The title compound was synthesized by a solid-state reaction at 1023 K in air. The crystal structure is isotypic with Mn(0.6)Zn(1.4)V(2)O(7) (C2/m; Z = 6) and is related to the crystal structure of thortveitite. The asymmetric unit contains two metal sites with statistically distributed magnesium and zinc atoms with the atomic ratio close to 1:1. One (Mg/Zn) metal site (M1) is located on Wyckoff position 8j and the other (M2) on 4h. Three V sites (all on 4i), and eight O (three 8j, four 4i, and one 2b) sites complete the asymmetric unit. The structure is an alternate stacking of V(2)O(7) layers and (Mg/Zn) atom layers along [20[Image: see text]]. It is distinct from other related structures in that each V(2)O(7) layer consists of two groups: a V(2)O(7) dimer and a V(4)O(14) tetramer. Mixed-occupied M1 and M2 are coordinated by oxygen atoms in distorted trigonal bipyramidal and octahedral sites, respectively. |
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