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Magnetoelectric coupling in artificial multiferroic interfaces can be drastically affected by the switching of oxygen vacancies and by the inversion of the ferroelectric polarization. Disentangling both effects is of major importance toward exploiting these effects in practical spintronic or spinorbitronic devices. We report on the independent control of ferroelectric and oxygen vacancy switching in multiferroic tunnel junctions with a La0.7Sr0.3MnO3 bottom electrode, a BaTiO3 ferroelectric barrier, and a Ni top electrode. We show that the concurrence of interface oxidation and ferroelectric switching allows for the controlled inversion of the interface spin polarization. Moreover, we show the possibility of a spin-memristor where the controlled oxidation of the interface allows for a continuum of memresistance states in the tunneling magnetoresistance. These results signal interesting new avenues toward neuromorphic devices where, as in practical neurons, the electronic response is controlled by electrochemical degrees of freedom.

Controlling magnetic anisotropy is an important objective towards engineering novel magnetic device concepts in oxide electronics. In thin film manganites, magnetic anisotropy is weak and it is primarily determined by the substrate, through induced structural distortions resulting from epitaxial mismatch strain. On the other hand, in cobaltites, with a stronger spin orbit interaction, magnetic anisotropy is typically much stronger. In this paper, we show that interfacing La0.7Sr0.3MnO3 (LSMO) with an ultrathin LaCoO3 (LCO) layer drastically modifies the magnetic anisotropy of the manganite, making it independent of the substrate and closer to the magnetic isotropy characterizing its rhombohedral structure. Ferromagnetic resonance measurements evidence a tendency of manganite magnetic moments to point out-of-plane suggesting non collinear magnetic interactions at the interface. These results may be of interest for the design of oxide interfaces with tailored magnetic structures for new oxide devices.

Thin films of ferromagnetic LTP-MnBi (Low Temperature Phase of MnBi) have been grown by magnetron sputtering onto quartz substrates. Two particular issues related to LTP-MnBi have been investigated: the strong influence of the growth temperature and the degradation of magnetic properties in time. The temperature dependence on the magnetic, morphological and microstructural properties has been investigated, evidencing drastic changes on the properties of MnBi with small temperature variations. By inducing a gradient of temperature during the growth, two well differentiated regions with different morphology and crystal structure have been observed in a MnBi film sample. On the other hand, aging experiments performed in a different LTP-MnBi sample has led to a notable decrease of 54% in the saturation magnetization after 6 days and a complete loss of ferromagnetic response after 4 months.

Ferromagnetic MnAl (L10-MnAl phase) ultrathin films with thickness varying from 1 to 5 nm have been epitaxially grown on a GaAs (001) substrate. A coercivity above 8 kOe has been obtained with no need of a buffer layer by tuning the sample preparation and the growth parameters. Surface and interface analysis carried out by in situ characterization techniques (x-ray photoelectron spectroscopy and low energy electron diffraction), available in the molecular beam epitaxy chamber, has shown the formation of a ferromagnetic interface consisting of Mn-Ga-As-Al, which contribution competes with the MnAl alloyed film. The appearance of this interface provides important information to understand the growth mechanism of MnAl-based films reported in the literature.