A high-pressure phase of vanadium pentoxide, denoted beta-V2O5, has been prepared at P = 6.0 GPa and T = 1073 K. The crystal structure of beta-V2O5 has been studied by X-ray and neutron powder diffraction, and high-resolution transmission electron microscopy. The V atoms are six-coordinated within distorted VO6 octahedra. The structure is built up of quadruple units of edge-sharing VO6 octahedra linked by sharing edges along [010] and mutually connected by sharing corners along [001]. This arrangement forms layers of V4O10 composition in planes parallel to (100). The layers are mutually held together by weak forces. beta-V2O5 is metastable and transforms to alpha-V2O5 at 643-653 K under ambient pressure. Structural relationships between beta- and alpha-V2O5, and between beta-V2O5 and B-Ta2O5-type structures are discussed. The high-pressure beta-V2O5 layer structure can be considered as the parent of a new series of vanadium oxide bronzes with cations intercalated between the layers.

A sample of Ta2O5, ditantalum pentaoxide, heat-treated in a "toroid"-type high-pressure chamber at P = 8 GPa and T = 1470 K, was studied by X-ray powder diffraction and high-resolution transmission electron microscopy (HRTEM). Two high-pressure modifications of Ta2O5, isostructural with B-Nb2O5 and Z-Nb2O5, were identified from the X-ray powder pattern. Both structures were refined by the Rietveld method from the X-ray diffraction data: B-Ta2O5, a = 12.7853 (4), b = 4.8537 (1), c = 5.5276 (2) A, beta = 104.264 (2)degrees, V = 332.45 A3, Z = 4, space group C2/c; Z-Ta2O5, a = 5.2252 (1), b = 4.6991 (1), c = 5.8534 (1) A, beta = 108.200 (2)degrees, V = 136.53 A3, Z = 2, space group C2. The Z-Ta2O5 modification is new. The Ta atoms are six-coordinated in B-Ta2O5 and seven-coordinated in Z-Ta2O5. The two structures are closely related, which makes an intergrowth and a transformation between them possible. An idealized model of the intergrowth structure has been given. The HRTEM study showed defect-rich B-Ta2O5 crystals, which could be interpreted as an intergrowth between the B-Ta2O5 and Z-Ta2O5 phases.

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A previous single-crystal X-ray and electron diffraction structure study [Rùmming et al. (1994). Acta Cryst. B50, 307±312] of the heavily faulted alloy phase -Al 4.5 FeSi has been extended by synchrotron powder data and further electron microscopy and diffraction observations. Re¯ections that were omitted in the single-crystal work could be included in the powder re®nement, which resulted in some adjustment of cell parameters and atom coordinates. The double c axis reported by some authors is explained by periodic faults in the structure, which is described in terms of a tetragonal sub-unit. Apparent discrepancies between re®nement from single-crystal and powder data are discussed brie¯y.

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