Endre søk
Link to record
Permanent link

Direct link
Publikasjoner (1 av 1) Visa alla publikasjoner
Yang, K., Kang, K., Diao, Z., Ramanathan, A., Karigerasi, M. H., Shoemaker, D. P., . . . Cahill, D. G. (2019). Magneto-optic response of the metallic antiferromagnet Fe2As to ultrafast temperature excursions. Physical Review Materials, 3(12), Article ID 124408.
Åpne denne publikasjonen i ny fane eller vindu >>Magneto-optic response of the metallic antiferromagnet Fe2As to ultrafast temperature excursions
Vise andre…
2019 (engelsk)Inngår i: Physical Review Materials, E-ISSN 2475-9953, Vol. 3, nr 12, artikkel-id 124408Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The linear magneto-optic Kerr effect (MOKE) is often used to probe magnetism of ferromagnetic materials, but MOKE cannot be applied to collinear antiferromagnets due to the cancellation of sublattice magnetization. Magneto-optic constants that are quadratic in magnetization, however, provide an approach for studying antiferromagnets on picosecond timescales. Here, we combine transient measurements of linear birefringence and optical reflectivity to study the optical response of Fe2As to small ultrafast temperature excursions. We performed temperature-dependent pump-probe measurements on crystallographically isotropic (001) and anisotropic (010) faces of Fe2As bulk crystals. We find that the largest optical signals arise from changes in the index of refraction along the z axis, perpendicular to the Ned vector. Both real and imaginary parts of the transient optical birefringence signal approximately follow the temperature dependence of the magnetic heat capacity, as expected if the changes in dielectric function are dominated by contributions of exchange interactions to the dielectric function.

HSV kategori
Identifikatorer
urn:nbn:se:su:diva-178673 (URN)10.1103/PhysRevMaterials.3.124408 (DOI)000504653600004 ()2-s2.0-85077324661 (Scopus ID)
Tilgjengelig fra: 2020-02-18 Laget: 2020-02-18 Sist oppdatert: 2022-11-02bibliografisk kontrollert
Identifikatorer
ORCID-id: ORCID iD iconorcid.org/0000-0001-5969-3460