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We report on the interplay between surface morphology and the magnetic properties of Pt/Mn ultra-thin bilayers by measuring the temperature dependence of the resistivity of Hall bars cooled under application of an external magnetic field. The resistivity (ρ) versus temperature (T) curves measured under a magnetic field applied along the x-, y- and z- directions exhibit a clear difference between the zero-field-cooled (ZFC) and field-cooled (FC) traces. The disparity between the ZFC and FC traces allowed us to determine the direction of the magnetic easy-axis. The ρ vs. T characteristic of the Pt/Mn bilayers revealed the existence of antiferromagnetic (AF) order below 79 K, in agreement with the Neel temperature observed in temperature dependent susceptibility curves. We also investigated the morphological evolution of the Mn films as a function of Mn thickness by atomic force microscopy (AFM). We observed the formation of a Mn layered structure on a 2nm-thick Al2O3 buffer layer for films thicker than 2.5 nm. Our results suggest that bilayer structures consisting of non-magnetic noble metals on ultra-thin antiferromagnetic metals can be used as a probe to explore the complex magnetic properties of the AF layer.

Non-magnetic (NM) metals with strong spin-orbit coupling have been recently explored as a probe of interface magnetism on ferromagnetic insulators (FMI) by means of the spin Hall magnetoresistance (SMR) effect. In NM/FMI heterostructures, increasing the spin mixing conductance (SMC) at the interface comes as an important step towards devices with maximized SMR. Here we report on the study of SMR in Pt/Fe3O4 bilayers at cryogenic temperature, and identify a strong dependence of the determined real part of the complex SMC on the interface roughness. We tune the roughness of the Pt/Fe3O4 interface by controlling the growth conditions of the Fe3O4 films, namely by varying the thickness, growth technique, and post-annealing processes. Field-dependent and angular-dependent magnetoresistance measurements sustain the clear observation of SMR. The determined real part of the complex SMC of the Pt/Fe3O4 bilayers ranges from 4.96 × 1014 Ω−1 m−2 to 7.16 × 1014 Ω−1 m−2 and increases with the roughness of the Fe3O4 underlayer. We demonstrate experimentally that the interface morphology, acting as an effective interlayer potential, leads to an enhancement of the spin mixing conductance.

Ex-situ and in-situ morphological analyses were performed for Cu-phthalocyanine (CuPc) organic semiconductor films by using atomic force microscopy (AFM) and reflection high-energy electron diffraction (RHEED). The focus was the effects of post-annealing on the structural characteristics of CuPc films grown on MgO(001) layers by using an ultra-high-vacuum thermal evaporator. Sphere-to-nanofibril and 2-D to 3-D morphological transitions were observed with increasing CuPc thickness beyond 3 nm. The surface morphology and the crystallinity were drastically improved after an additional cooling of the post-annealed CuPc films thinner than 3 nm. Our results highlight that molecular orientation and structural ordering can be effectively controlled by using different temperature treatments and a proper combination of material, film thickness, and substrate.

Tuning the magnetoresistance behavior of heterostructures composed of nonmagnetic and ferromagnetic (FM) materials is crucial for improving their applicability in electronic and spintronic devices. In this study, we investigate whether the integration of organic layers to NiFe/Pt junctions can result in the modification of the magnetic moment of the FM layer using iron phthalocyanines (FePc) and copper phthalocyanines (CuPc) as the interfacial layers for controlling the spin-charge conversion. Relaxation of the out-of-plane magnetic hard axis of the NiFe/Pt junctions is observed, as a result of the modification of the interfacial magnetic structure. The transport measurements of the fabricated hybrid Hall bar junctions with NiFe/FePc/Pt and NiFe/CuPc/Pt reveal that although the intrinsic anisotropic magnetoresistance of the present Hall bar is maintained with the integration of interfacial metal phthalocyanine (MPc) layers, a change in the magnetic response along the axis perpendicular to the in-plane of Hall bars is observed, owing to the insertion of the interfacial MPc layers. The present method of interface engineering via integration of organic interfacial layers can act as a model system for controlling the spin-charge conversion behavior of magnetic heterojunction toward the development of multifunctional molecular-engineered spintronic devices.