Lateral modulation of magnetic anisotropy in tricolor 3d-5d oxide superlattices

Abstract

Manipulating magnetic anisotropy (MA) purposefully in transition metal oxides (TMOs) enables the development of oxide-based spintronic devices with practical applications. Here, we report a pathway to reversibly switch the lateral magnetic easy-axis via interfacial oxygen octahedral coupling (OOC) effects in 3d-5d tricolor superlattices, i.e. [SrIrO3,mRTiO3,SrIrO3,2La0.67Sr0.33MnO3]10 (RTiO3: SrTiO3 and CaTiO3). In the heterostructures, the anisotropy energy (MAE) is enhanced over one magnitude to ~106 erg/cm3 compared to La0.67Sr0.33MnO3 films. Moreover, the magnetic easy-axis is reversibly reoriented between (100)- and (110)-directions by changing the RTiO3. Using first-principles density functional theory calculations, we find that the SrIrO3 owns a large single-ion anisotropy due to its strong spin-orbit interaction. This anisotropy can be reversibly controlled by the OOC, then reorient the easy-axis of the superlattices. Additionally, it enlarges the MAE of the films via the cooperation with a robust orbital hybridization between the Ir and Mn atoms. Our results indicate that the tricolor superlattices consisting of 3d and 5d oxides provide a powerful platform to study the MA and develop oxide-based spintronic devices.

References in corpus (7)

• Emerging magnetism and anomalous Hall effect in iridate-manganite heterostructures
• Tuning Perpendicular Magnetic Anisotropy by Oxygen Octahedral Rotations in (La${}_{1-x}$Sr${}_x$MnO${}_3$)/(SrIrO${}_3$) Superlattices
• Atomically flat single terminated oxide substrate surfaces
• Dimensionality-driven metal-insulator-transition in spin-orbit coupled SrIrO${}_3$
• Charge transfer driven emergent phenomena in oxide heterostructures
• Charge transfer in iridate-manganite superlattices
• Interfacial-hybridization-modified Ir Ferromagnetism and Electronic Structure in LaMnO${}_3$/SrIrO${}_3$ Superlattices