Li, Man-Rong, McCabe, E. E., Stephens, Peter W., Croft, Mark, Collins, Liam, Kalinin, Sergei V., Deng, Zheng, Retuerto, Maria, Sen Gupta, Arnab, Padmanabhan, Haricharan, and others. (2017) Magnetostriction-polarization coupling in multiferroic Mn2MnWO6. Nature Communications, 8 (1). ISSN 2041-1723. (doi:10.1038/s41467-017-02003-3) (KAR id:65337)
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| Official URL: https://doi.org/10.1038/s41467-017-02003-3 |
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Abstract
Double corundum-related polar magnets are promising materials for multiferroic and magnetoelectric applications in spintronics. However, their design and synthesis is a challenge, and magnetoelectric coupling has only been observed in Ni3TeO6 among the known double corundum compounds to date. Here we address the high-pressure synthesis of a new polar and antiferromagnetic corundum derivative Mn2MnWO6, which adopts the Ni3TeO6-type structure with low temperature first-order field-induced metamagnetic phase transitions (TN?=?58?K) and high spontaneous polarization (~ 63.3 ?C·cm?2). The magnetostriction-polarization coupling in Mn2MnWO6 is evidenced by second harmonic generation effect, and corroborated by magnetic-field-dependent pyroresponse behavior, which together with the magnetic-field-dependent polarization and dielectric measurements, qualitatively indicate magnetoelectric coupling. Piezoresponse force microscopy imaging and spectroscopy studies on Mn2MnWO6 show switchable polarization, which motivates further exploration on magnetoelectric effect in single crystal/thin film specimens.
| Item Type: | Article |
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| DOI/Identification number: | 10.1038/s41467-017-02003-3 |
| Subjects: | Q Science |
| Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
| Depositing User: | Emma McCabe |
| Date Deposited: | 12 Dec 2017 17:54 UTC |
| Last Modified: | 05 Nov 2024 11:02 UTC |
| Resource URI: | https://kar.kent.ac.uk/id/eprint/65337 (The current URI for this page, for reference purposes) |
University of Kent Author Information
McCabe, E. E..
| Creator's ORCID: |
 https://orcid.org/0000-0001-5868-4570
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