Published June 9, 2014 | Version v1
Journal article

Asymmetric "melting" and "freezing" kinetics of the magnetostructural phase transition in B2-ordered FeRh epilayers

  • 1. School of Chemistry, University of Edinburgh, Edinburgh EH9 3JJ (United Kingdom)
  • 2. School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT (United Kingdom)
  • 3. Department of Chemical Engineering, Northeastern University, Boston, Massachusetts 02115 (United States)
  • 4. Institute for Materials Research, University of Leeds, Leeds LS2 9JT (United Kingdom)
  • 5. Collaborative Innovation Center of Quantum Matter, Beijing 100871 (China)
  • 6. Beijing National Laboratory for Condensed Matter Physics, and Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China)
  • 7. Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, New York 11973 (United States)
  • 8. ISIS, Harwell Science and Innovation Campus, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Didcot, Oxon OX11 0QX (United Kingdom)

Description

Synchrotron X-ray diffraction was used to study the phase transformation processes during the magnetostructural transition in a B2-ordered FeRh (001)-oriented epilayer grown on MgO by sputtering. Out-of-plane lattice constant measurements within the hysteretic regime of the transition reveal a microstructure consistent with the coexistence of lattice-expanded and contracted phases in spatially distinct regions. It was found that the phase separation is more pronounced during cooling than heating. Furthermore, whilst lattice-expanded domains that span the height of the film can be undercooled by several kelvins, there is no equivalent superheating. This asymmetry between the cooling and heating processes in FeRh is consistent with the difference in the kinetics of generic freezing and melting transitions.

Additional details

Identifiers

Publishing Information

Journal Title
Applied Physics Letters
Journal Volume
104
Journal Issue
23
Journal Page Range
p. 232407-232407.5
ISSN
0003-6951
CODEN
APPLAB

Optional Information

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