A Study of the Intermetallic Compounds of Gold and Manganese through the Use of the Au197 Mössbauer Effect at 4.2°K and as a Function of Pressure

David O. Patterson, J. O. Thomson, P. G. Huray, and Louis D. Roberts
Phys. Rev. B 2, 2440 – Published 1 October 1970
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Abstract

The Mössbauer spectra of the Au197 nuclei in Au, Au4Mn, Au3Mn, Au2Mn, AuMn, AuMn3, and dilute alloys of Au in Mn have been measured at 4.2 °K. The isomer shift, magnetic dipole, and electric quadrupole splittings observed for these alloys are discussed in terms of the magnetic and crystalline structure. In these ordered gold-manganese alloys, the isomer shift as a function of composition departs widely from the linearity often observed for gold solid-solution alloys. For Au2Mn, we find an effective field at the Au197 nucleus of 1590 kG as well as a large quadrupole coupling. The spectrum we observe for Au2Mn is consistent with the helical magnetic structure generally assumed for this alloy. A detailed analysis of this spectrum gives the magnetic moment μ*=0.415±0.004 μN for the 77.345-keV state of Au197, subject to a correction for the hyperfine-structure anomaly. For Au2Mn, Mössbauer measurements have also been made as a function of pressure between 0 and 46 kbars. A 7% increase in the magnitude of the effective field at the Au197 nucleus is observed between 0 and 30 kbar. This may be due to the uncoiling of the Mn spin helix observed by other workers in this pressure range.

  • Received 26 May 1969

DOI:https://doi.org/10.1103/PhysRevB.2.2440

©1970 American Physical Society

Authors & Affiliations

David O. Patterson* and J. O. Thomson

  • Oak Ridge National Laboratory, Oak Ridge, Tennessee
  • University of Tennessee, Knoxville, Tennessee

P. G. Huray and Louis D. Roberts

  • Oak Ridge National Laboratory, Oak Ridge, Tennessee
  • University of Tennessee, Knoxville, Tennessee
  • University of North Carolina, Chapel Hill, North Carolina

  • *Oak Ridge Graduate Fellow from the University of Tennessee under appointment with Oak Ridge Associated Universities. Present address: Radiation Inc., P. O. Box 37, Melbourne, Fla.
  • Present address: Physics Department, University of Tennessee, Knoxville, Tenn.
  • Present address: Physics Department, University of North Carolina, Chapel Hill, N. C.

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Issue

Vol. 2, Iss. 7 — 1 October 1970

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