Volume 127, Issue 41 pp. 12242-12245
Zuschrift

Large Magnetization and Frustration Switching of Magnetoresistance in the Double-Perovskite Ferrimagnet Mn2FeReO6

Dr. Angel M. Arévalo-López

Dr. Angel M. Arévalo-López

Centre for Science at Extreme Conditions (CSEC) and School of Chemistry, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JZ (UK)

Search for more papers by this author
Graham M. McNally

Graham M. McNally

Centre for Science at Extreme Conditions (CSEC) and School of Chemistry, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JZ (UK)

Search for more papers by this author
Prof. J. Paul Attfield

Corresponding Author

Prof. J. Paul Attfield

Centre for Science at Extreme Conditions (CSEC) and School of Chemistry, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JZ (UK)

Centre for Science at Extreme Conditions (CSEC) and School of Chemistry, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JZ (UK)Search for more papers by this author
First published: 26 August 2015
Citations: 9

Abstract

Ferrimagnetic A2BB′O6 double perovskites, such as Sr2FeMoO6, are important spin-polarized conductors. Introducing transition metals at the A-sites offers new possibilities to increase magnetization and tune magnetoresistance. Herein we report a ferrimagnetic double perovskite, Mn2FeReO6, synthesized at high pressure which has a high Curie temperature of 520 K and magnetizations of up to 5.0 μB which greatly exceed those for other double perovskite ferrimagnets. A novel switching transition is discovered at 75 K where magnetoresistance changes from conventional negative tunneling behavior to large positive values, up to 265 % at 7 T and 20 K. Neutron diffraction shows that the switch is driven by magnetic frustration from antiferromagnetic Mn2+ spin ordering which cants Fe3+ and Re5+ spins and reduces spin-polarization. Ferrimagnetic double perovskites based on A-site Mn2+ thus offer new opportunities to enhance magnetization and control magnetoresistance in spintronic materials.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.