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Magnetic Structure and Ordering of Multiferroic Hexagonal LuFeO3

  • Steven M. Disseler
  • , Julie A. Borchers
  • , Charles M. Brooks
  • , Julia A. Mundy
  • , Jarrett A. Moyer
  • , Daniel A. Hillsberry
  • , Eric L. Thies
  • , Dmitri A. Tenne
  • , John Heron
  • , Megan E. Holtz
  • , James D. Clarkson
  • , Gregory M. Stiehl
  • , Peter Schiffer
  • , David A. Muller
  • , Darrell G. Schlom
  • , William D. Ratcliff
  • National Institute of Standards and Technology
  • Cornell University
  • University of Illinois at Urbana-Champaign
  • Boise State University
  • University of California at Berkeley

Research output: Contribution to journalArticlepeer-review

111 Scopus citations

Abstract

We report on the magnetic structure and ordering of hexagonal LuFeO 3 films of variable thickness grown by molecular-beam epitaxy (MBE) on YSZ (111) and Al 2 O 3 (0001) substrates. These crystalline films exhibit long-range structural uniformity dominated by the polar P 6 3 cm phase, which is responsible for the paraelectric to ferroelectric transition that occurs above 1000 K. Using bulk magnetometry and neutron diffraction, we find that the system orders into a ferromagnetically-canted antiferromagnetic state via a single transition below 155 K regardless of film thickness, which is substantially lower than that previously reported in hexagonal LuFeO 3 films. The symmetry of the magnetic structure in the ferroelectric state implies that this material is a strong candidate for linear magnetoelectric coupling and control of the ferromagnetic moment directly by an electric field.

Original languageAmerican English
Article number217602
JournalPhysical Review Letters
Volume114
Issue number21
DOIs
StatePublished - 27 May 2015

EGS Disciplines

  • Physics

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