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The field of oxide spintronics can strongly benefit from the establishment of ferromagnetic insulators with near room-temperature Curie temperature. Here, we investigate the structural, electronic, and magnetic properties of epitaxially strained thin films of the double perovskite La2NiMnO6 (LNMO) grown by off-axis radio-frequency magnetron sputtering. We find that the films retain insulating behavior and a bulk-like Curie temperature in the order of 280 K independently of the epitaxial strain conditions. These results suggest a prospective implementation of LNMO films in multi-layer device architectures where a high-temperature ferromagnetic insulating state is a prerequisite.

A strong coupling of the lattice to functional properties is observed in many transition metal oxide systems, such as the ABO3 perovskites. In the quest for tailor-made materials, it is essential to be able to control the structural properties of the compound(s) of interest. Here, thin film solid solutions that combine NdNiO3 and LaNiO3, two materials with the perovskite structure but distinct space groups, are analyzed. Raman spectroscopy and scanning transmission electron microscopy are combined in a synergistic approach to fully determine the mechanism of the structural crossover with chemical composition. It is found that the symmetry transition is achieved by phase coexistence in a way that depends on the substrate selected. These results carry implications for analog-tuning of physical properties in future functional materials based on these compounds.

Nanoscale mapping of the distinct electronic phases characterizing the metal–insulator transition displayed by most of the rare-earth nickelate compounds is fundamental for discovering the true nature of this transition and the possible couplings that are established at the interfaces of nickelate-based heterostructures. Here, we demonstrate that this can be accomplished by using scanning transmission electron microscopy in combination with electron energy-loss spectroscopy. By tracking how the O K and Ni L edge fine structures evolve across two different NdNiO 3 /SmNiO 3 superlattices, displaying either one or two metal–insulator transitions depending on the individual layer thickness, we are able to determine the electronic state of each of the individual constituent materials. We further map the spatial configuration associated with their metallic/insulating regions, reaching unit cell spatial resolution. With this, we estimate the width of the metallic/insulating boundaries at the NdNiO 3 /SmNiO 3 interfaces, which is measured to be on the order of four unit cells.

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We use resonant soft x-ray diffraction to track the photoinduced dynamics of the antiferromagnetic structure in a NdNiO 3 thin film. Femtosecond laser pulses with a photon energy of 0.61 eV, resonant with electron transfer between long-bond and short-bond nickel sites, are used to excite the material and drive an ultrafast insulatormetal transition. Polarization-sensitive soft x-ray diffraction, resonant to the nickel L 3 edge, then probes the evolution of the underlying magnetic spiral as a function of time delay with 80 ps time resolution. By modeling the azimuthal dependence of the scattered intensity for different linear x-ray polarizations, we benchmark the changes of the local magnetic moments and the spin alignment. The measured changes are consistent with a reduction of the long-bond site magnetic moments and an alignment of the spins towards a more collinear structure at early time delays.

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