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 NiTeO among the known double corundum compounds to date. Here we address the high-pressure synthesis of a new polar and antiferromagnetic corundum derivative MnMnWO, which adopts the NiTeO-type structure with low temperature first-order field-induced metamagnetic phase transitions (T = 58 K) and high spontaneous polarization (~ 63.3 μC·cm). The magnetostriction-polarization coupling in MnMnWO 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 MnMnWO show switchable polarization, which motivates further exploration on magnetoelectric effect in single crystal/thin film specimens.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725588 | PMC |
http://dx.doi.org/10.1038/s41467-017-02003-3 | DOI Listing |
Nat Commun
December 2017
Department of Chemistry and Chemical Biology, Rutgers, the State University of New Jersey, 610 Taylor Road, Piscataway, NJ, 08854, USA.
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 NiTeO among the known double corundum compounds to date. Here we address the high-pressure synthesis of a new polar and antiferromagnetic corundum derivative MnMnWO, which adopts the NiTeO-type structure with low temperature first-order field-induced metamagnetic phase transitions (T = 58 K) and high spontaneous polarization (~ 63.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!