Charge transfer in perovskite oxide heterostructures could break the delicate balance among charge, spin, orbital and lattice order at the interface, producing exotic phenomena that cannot be observed in bulk materials. Here, opposite interfacial charge transfer directions are observed in SrIrO3/NdNiO3 and SrIrO3/LaNiO3 3d/5d perovskite heterostructures. This is accompanied with an inverse change of Ni eg orbital polarization and Ni-O pd hybridization across the interface, by stretching/compressing the out-of-plane Ni-O bond in the opposite internal electrical field due to the opposite electron transfer direction. These interfacial reconstructions finally bring about a manipulation on the transport and magnetic characteristics. This work reveals that A site cation in perovskite heterostructures could be a knob to control the interfacial charge transfer direction, and the 3d/5d perovskite interfaces are excellent platform to study the complex interplay between various order parameters and stimulate novel interfacial effects.
We reported a peculiar thickness dependence of perpendicular magnetic anisotropy (PMA), stronger in thinner films, in spinel NiCo2O4 (NCO) films deposited epitaxially on MgAl2O4 (001) single crystalline substrates. The effective PMA field is about 3 T in 23.0 nm-thick films but increases dramatically to about 7 T in 4.5 nm-thick films. X-ray absorption spectra reveal an inhomogeneous distribution of Co2+ cations along the film's normal with more Co2+ adjacent to the film/substrate interface. X-ray linear dichroism spectra reveal that the PMA in NCO films is associated with electrons occupying the x2–y2 orbital of Co cations at the tetrahedral sites. This work demonstrates the potential of ultrathin NCO films in all-oxide spintronic devices.
Strong Coulomb repulsion and spin-orbit coupling are known to give rise to exotic physical phenomena in transition metal oxides. Here, we report magnetic and transport characteristics of (001) oriented epitaxial SrMnxIr1-xO3 thin films, having both 3d and 5d elements on the perovskite B sites. With the increase of Mn concentration, perpendicular magnetic anisotropy decreases gradually in accompany with the magnetic easy axis tilting away from the out-of-plane [001] direction. X-ray absorption spectroscopy reveals that Mn eg electrons preferentially occupy the "d" _(〖"3z" 〗^"2" "-" "r" ^"2" ) orbital, which produces the observed perpendicular magnetic anisotropy in the framework of spin-orbital coupling. A planar topological Hall effect appears in SrMnxIr1-xO3 films with x about 0.30 when the magnetic field is applied along the current, which is a result of the noncoplanar spin structure due to the competition among the perpendicular magnetic anisotropy, the magnetic exchange interaction and the Zeeman energy. These results provide an example to show the subtle balance among complex competitions in materials with both strong correlation and spin-orbit coupling.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.