Published December 1, 1995 | Version v1
Journal article

Chromium clustering and ordering in Hg1-xCrxSr2CuO4+δ

  • 1. Materials Science Division and Science and Technology Center for Superconductivity, Argonne National Laboratory, Argonne, Illinois 60439 (United States)
  • 2. Department of Materials Science and Engineering and Science and Technology Center for Superconductivity, Northwestern University, Evanston, Illinois 60208 (United States)
  • 3. Physics Department, Northern Illinois University, DeKalb, Illinois 60115 (United States)

Description

Solid-solution compounds where Cr, Re, and other metals are substituted for Hg in Hg-Ca-Ba-Cu-O superconductors have been reported to exhibit enhanced flux-pinning behavior. We have determined the structural modifications resulting from the incorporation of Cr in Hg1-xCrxSr2CuO4+δ (for x∼0.4) using neutron powder diffraction, electron diffraction, and lattice imaging. Cr substitutes at the Hg site, but is displaced to allow tetrahedral coordination by oxygen atoms. Additional oxygen is incorporated to provide four oxygen atom neighbors for each Cr atom. These CrO4 units cluster to form a supercell of approximate dimensions 5ax5ax2c in which Cr-rich and Hg-rich regions alternate in all three crystallographic directions. Because the Cu-O apical bond associated with the CrO4 unit is lengthened to 3.13 A, the superconducting planes are best viewed as consisting of CuO5 pyramids, oriented up or down as dictated by the supercell ordering, rather than CuO6 octahedra. Local structural constraints associated with individual Cr sites require that considerable disorder is present, even in the supercell. Extended defects in this supercell (e.g., columns of CuO6 octahedra associated with Hg-rich regions) may contribute to the enhanced flux pinning

Additional details

Publishing Information

Journal Title
Physical Review. B, Condensed Matter
Journal Volume
52
Journal Issue
21
Journal Page Range
p. 15636-15643.
ISSN
0163-1829
CODEN
PRBMDO