Volume 54, Issue 41 pp. 12074-12077
Communication

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)

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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)

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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: 77

Graphical Abstract

Double-perovskite magnetism: The double perovskite Mn2FeReO6 synthesized at high pressure has magnetic transition-metal cations at all sites. High-spin Mn2+ cations lead to record magnetizations for double-perovskite ferrimagnets and their frustrated magnetic order at 75 K switches magnetoresistance from negative to large positive values at low temperatures.

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.

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