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Published on: June 12, 2019
High pressure exploration in the Li-Ln-V-O system
A I Zadoya1, Á M Arévalo-López1, J Sánchez-Benítez2
1Université de Lille, CNRS, Centrale Lille, Université d'Artois, Unité de Catalyse et Chimie du Solide, Lille, F-59000, France. marie.colmont@centralelille.fr.
Abstract:
Using in situ high pressure Raman spectroscopy, two structural changes were observed in a sample of the composition LiLa5O5(VO4)2. Taking this into account and by combining different conditions, three new compounds were further obtained from high pressure-high temperature synthesis. Their crystal structure description was done using the antiphase approach, which implies the presence of oxygen-centered [OLn4] building units, where Ln is La for (1) β-LiLa5O5(VO4)2 and (2) β-LiLa2O2(VO4) or Nd for (3) LiNd5O5(VO4)2 compounds. (1) crystallizes in the triclinic space group P1[combining macron] with unit cell parameters of a = 5.8167(15) Å, b = 12.2954(28) Å, c = 18.7221(69) Å, α = 102.03(2)°, β = 98.76(2)°, and γ = 103.54(2)°; a 3D structure was deduced from the ambient pressure polymorph. (2) also crystallizes in P1[combining macron] with a = 5.8144(7) Å, b = 5.8167(7) Å, c = 8.5272(1) Å, α = 98.184(7)°, β = 100.662(7)° and γ = 92.579(7)°. It shows a 2D structure with [La2O2]2+ layers surrounded by [LiO4] and [VO4] tetrahedra sharing corners and edges. (3) exhibits a 3D architecture isotypic with AP-LiLa5O5(VO4)2. The crucial role of high pressure in such types of synthesis and materials is also discussed.
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