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Synthesis and structural characterisation of YSr2Cu3−xMxO7±y (M = Fe, Ti, Al, Co, Ga, Pb; 0.5 < x < 1), and the non-existence of the parent phase YSr2Cu3O7

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TLDR
The possibility of synthesizing phases of general composition YSr 2 Cu 3− x M x O 7± y has been examined for a wide variety of metals M.
Abstract
The possibility of synthesising phases of general composition YSr 2 Cu 3− x M x O 7± y has been examined for a wide variety of metals M. Single phase tetragonal products (typically a = 3.83 A , c = 11.5 A ) can be synthesised provided that the concentration of M is sufficiently large ( x > 0.5), and M has a preference for the Cu(1) sites (the four-coordinate sites) of the YBa 2 Cu 3 O 7 , structure. Neutron diffraction has demonstrated that a high degree of disorder exists in the (001) planes containing the M cations and, in particular, significant oxygen displacements are found. The non-existence of the unsubstituted variant YSr 2 Cu 3 O 7 is explained in terms of the high degree of compressive stress on the Cu(1) sites which could exist in such a material.

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Ruthenium-based layered cuprates RuSr2LnCu2O8 and RuSr2(Ln1+xCe1−x)Cu2O10 (LnSm, Eu and Gd)

TL;DR: In this article, the authors synthesized layered cuprates where the intermediate layer between the CuO 2 blocks consists of vertex sharing RuO 6 octahedra, where the analogy to the isostructural Nb based compounds, as well as simple valence counting, suggest that Ru is pentavalent in these compounds.
Journal ArticleDOI

Preparation and properties of YSr2Cu3−xMxOy (M = Li, Al, Ti, V, Cr, Fe, Co, Ga, Ge, Mo, WandRe)

TL;DR: In this article, the authors investigated the composition YSr2Cu3-xMxOy and obtained the 123-structure for M= Li, Al, Ti, V, Cr, Fe, Co, Ga, Ge, Mo, W and Re.
Journal ArticleDOI

Hole-doped cuprate high temperature superconductors

TL;DR: In this article, the major cuprate materials systems that have laid the foundation of high temperature superconductivity (HTS) science and technology and present several simple scaling laws that show the systematic and universal simplicity amid the complexity of these material systems.
Journal ArticleDOI

Crystal chemical substitutions and doping of YBa2CU3Ox and related superconductors

TL;DR: A review of the literature on substitutions and their effect on the properties of the 90 K superconductor YBa 2 Cu 3 O δ (YBCO) can be found in this paper.
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Epitaxial Strain-Induced Chemical Ordering in La0.5Sr0.5CoO3−δ Films on SrTiO3

TL;DR: In this article, the authors used synchrotron X-ray diffraction to show that a 40-nm thin film of perovskite La 0.5Sr0.5CoO3−δ has an ordered phase at 650 K. The ordered phase consists of La and Sr cations in planes parallel to the surface and is associated with coherent expansion in the c-direction.
References
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Journal ArticleDOI

Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides

TL;DR: The effective ionic radii of Shannon & Prewitt [Acta Cryst. (1969), B25, 925-945] are revised to include more unusual oxidation states and coordinations as mentioned in this paper.
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Structure of the 100 K Superconductor Ba2YCu3O7 between (5 ÷ 300) K by Neutron Powder Diffraction

TL;DR: In this article, the authors used profile refinement of high-resolution neutron powder data at six different temperatures between 5 K and 300 K to refine the structure of a pure and well-characterised powder sample with onset of superconductivity at 100 K.
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Structure and crystal chemistry of the high-Tc superconductor YBa2Cu3O7−x

TL;DR: In this article, high-resolution neutron powder diffraction data for this phase with x = 0.15(7) were presented, and the results agree with ref. 4 with respect to cation positions, but the location of one set of oxygen defects is substantially different and necessitates the lowering of lattice symmetry from tetragonal to orthorhombic (space group Pmmm).
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Bulk superconductivity up to 122 K in the Tl-Pb-Sr-Ca-Cu-O system

TL;DR: New high-temperature superconductors based on oxides of thallium and copper, but not containing barium, have been prepared with structure refinement carried out with single-crystal x-ray diffraction data.
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