Published July 8, 2024 | Version v1
Journal article

Spin-flop coupling at La0.5Sr0.5FeO3/La0.7Sr0.3MnO3 interfaces

  • 1. Department of Materials Science and Engineering, University of California, Davis, Davis, California 95616, USA
  • 2. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA
  • 3. Brookhaven National Laboratory, Upton, New York 11973, USA

Description

Antiferromagnetic (AFM) spintronics offer several benefits compared to their ferromagnetic (FM) counterparts, such as high storage capacity and faster processing speed, however, difficulties in manipulating and detecting the AFM moments impede their implementation. Spin-flop coupling, the interfacial perpendicular coupling between FM and AFM moments, can be utilized to control the orientation of AFM moments with the application of moderate magnetic fields on the scale of tenths of a Tesla. In this work, epitaxial bilayers of AFM La0.5Sr0.5FeO3 (LSFO)/FM La0.7Sr0.3MnO3 (LSMO) with fixed LSMO thickness (85 u.c.) and LSFO thicknesses varying from 10 to 50 u.c. were investigated to determine the effect of Sr doping and La1xSrxFeO3 magnetocrystalline anisotropy on the strength of spin-flop coupling. X-ray magnetic linear dichroism demonstrated that the spin-flop coupling strength decreased with increasing LSFO layer thickness, persisting at a thickness of 50 u.c. (20 nm). Furthermore, photoemission electron microscopy revealed a domain-by-domain correlation between the FM and AFM domains consistent with the perpendicular orientation dictated by spin-flop coupling. These results demonstrate that LSFO/LSMO bilayers have the potential to serve as a model materials system for AFM spin transport measurements.

Additional details

Identifiers

DOI
10.1103/PhysRevB.110.014411;
Crossref Funder ID
10.13039/100000001; 10.13039/100000015;

Publishing Information

Journal Title
Physical Review B
Journal Volume
110
Journal Issue
1
Journal Page Range
8 pgs.
ISSN
1550-235X

Optional Information

Copyright
©2024 American Physical Society
Contract/Grant/Project number
DMR-2004704; DE-AC02-05CH11231
Notes
Record automatically processed
Funding organization
National Science Foundation; U.S. Department of Energy