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A superconductor exhibiting a polarity-dependent critical current is of fundamental as well as technological interest, because the superconducting (SC) layer can then admit a perfect dissipationless transmission along one direction while offering a large resistance along the opposite, leading to a phenomenon called SC diode effect or rectification. Here we demonstrate that SC diode effects are ubiquitous in superconductors and observable in a large variety of settings. Controllable via an out-of-plane magnetic field, we observe an extremely sensitive SC diode effect (type A) in superconducting vanadium or niobium stripes with symmetry breaking between their two edges. Nonreciprocity of critical current results from an out-of-plane field as small as 1 Oe, while the diode efficiency and polarity are manipulated via the strength and direction of the field. With the out-of-plane field carefully eliminated, an in-plane field also creates a sizeable asymmetry between critical currents (type B), regardless of whether this field is perpendicular or parallel to the current flow direction. Finally, we demonstrate nonreciprocal critical currents with a giant diode efficiency reaching 65% when the SC V film couples to a ferromagnetic EuS layer with in-plane magnetization orthogonal to current flow (type C) and a clear diode rectification is seen. This is also realized at zero applied field, in the remnant magnetic state of EuS. Our observations show the ubiquity of the superconducting diode effect, and pave the way for the development of versatile SC rectifiers employing simple structures using widely available materials.

Multiple magnetic skyrmion phases add an additional degree of freedom for skyrmion-based ultrahigh-density spin memory devices. Extending the field to 2D van der Waals magnets is a rewarding challenge, where the realizable degree of freedoms (e.g., thickness, twist angle, and electrical gating) and high skyrmion density result in intriguing new properties and enhanced functionality. In this work, a van der Waals interface, formed by two 2D ferromagnets Cr2 Ge2 Te6 and Fe3 GeTe2 with a Curie temperature of ≈65 and ≈205 K, respectively, hosting two groups of magnetic skyrmions, is reported. Two sets of topological Hall effect signals are observed below 6s0 K when Cr2 Ge2 Te6 is magnetically ordered. These two groups of skyrmions are directly imaged using magnetic force microscopy, and supported by micromagnetic simulations. Interestingly, the magnetic skyrmions persist in the heterostructure with zero applied magnetic field. The results are promising for the realization of skyrmionic devices based on van der Waals heterostructures hosting multiple skyrmionphases.

Metal-oxide nanostructures play a fundamental role in a large number of technological applications, ranging from chemical sensors to data storage devices. As the size of the devices shrinks down to the nanoscale, it is mandatory to obtain sharp and good quality interfaces. Here, it is shown that a two-dimensional material, namely, graphene, can be exploited as an ideal buffer layer to tailor the properties of the interface between a metallic substrate and an ultrathin oxide. This is proven at the interface between an ultrathin film of the magnetoelectric antiferromagnetic oxide Cr2O3 and a Ni(111) single crystal substrate. The chemical composition of the samples has been studied by means of X-ray photoemission spectroscopy, showing that the insertion of graphene, which remains buried at the interface, is able to prevent the oxidation of the substrate. This protective action leads to an ordered and layer-by-layer growth, as revealed by scanning tunneling microscopy data. The structural analysis performed by low-energy electron diffraction indicates that the oxide layer grown on graphene experiences a significant compressive strain, which strongly influences the surface electronic structure observed by scanning tunneling spectroscopy.

In this paper we focus on the structural, electronic, and magnetic properties of Ni tetra-phenyl-porphyrins (NiTPP) grown on top of Fe(001)–p(1 × 1)O. Ordered thin films of metal TPP molecules are potentially interesting for organic electronic and spintronic applications, especially when they are coupled to a ferromagnetic substrate. Unfortunately, porphyrin layers deposited on top of ferromagnetic substrates do not generally show long-range order. In this work, we provide evidence of an ordered disposition of the organic film above the iron surface and we prove that the thin layer of iron oxide decouples the molecules from the substrate, thus preserving the molecular electronic features, especially the HOMO-LUMO gap, even when just a few organic layers are deposited. The effect of the exposure to molecular oxygen is also investigated and an increased robustness against oxidation with respect to the bare substrate is detected. Finally, we present our results for the magnetic analysis performed by spin resolved spectroscopy, finding a null magnetic coupling between the molecules and the substrate.

The reduction and oxidation of epitaxial Fe3O4 films grown by reactive deposition on a Fe-p(1 × 1)O surface have been investigated by means of Auger electron spectroscopy (AES), low energy electron diffraction (LEED) and scanning tunneling microcopy (STM). The as-grown iron oxide samples display a square LEED pattern with a lattice constant compatible with a p(1 × 1) bulk terminated Fe3O4(001) surface. STM topographic images of Fe3O4 are characterized by atomically flat terraces separated by highly oriented steps running along the (010) and (100) crystallographic directions of the substrate. Upon annealing at 800 K in an ultra-high vacuum, AES reveals that magnetite transforms to FeO. The sample exposes the (001) surface of the rock salt structure, with a lattice parameter close to that of bulk wustite. The Fe3O4 phase can be recovered by oxidation at 10−6 mbar of molecular oxygen.

We give evidence of the formation of an ordered array of tetra-phenyl porphyrins (TPP) when these molecules are deposited on top of oxygen-passivated Fe(001), namely the Fe(001)-p(1 × 1)O surface. We also prove that they are magnetically coupled with the substrate. The ordered molecular packing, together with the magnetic coupling, are fundamental conditions for application in organic spintronic devices. The system is studied by means of spin-resolved photoemission spectroscopies and scanning tunneling microscopy.

We present a multitechnique investigation of the structural and electronic properties of the prototypical system composed by ultra-thin films of magnetic molecules [Co-tetraphenyl-porphyrins (Co-TPP)] grown on a ferromagnetic substrate [oxygen passivated Fe(0 0 1), namely the Fe(0 0 1)-p(1 × 1)O surface]. Low Energy electron diffraction (LEED) and scanning tunneling microscopy (STM), coupled with first-principles calculations, reveal the formation of a commensurate superstructure at monolayer coverage, made by a square array of flat-lying TPP molecules. UV–photoemission and inverse photoemission spectroscopies (UPS and IPES) are used to investigate their electronic structure. Similar to our previous results on the Zn–TPP growth on Fe(0 0 1)–p(1 × 1)O, the passivation of the metallic surface is able to preserve the photoemission features characteristic of quasi-free molecules, opening the route towards an exploitation of single oxide layers as protective films in organic/inorganic junctions. X-ray photoemission (XPS) and near edge X-ray adsorption fine structure spectroscopies (NEXAFS), are used to reveal the details of the Co–TPP interaction with the substrate., We acknowledge the CINECA award under the ISCRA initiative, for the availability of high performance computing resources and support (Application No. HP10C2SVDP).

We propose a method to grow metal tetraphenyl porphyrin (MTPP) molecular layers where a long-range structural and magnetic order can be achieved simultaneously and at room temperature by a proper treatment of the ferromagnetic substrate. We focus in particular on the oxygen-passivated Fe(001)-p(1 × 1)O surface, where MTPP molecules (with M=Co and Ni) arrange by forming square commensurate overlayers. Spin-resolved photoemission detects a clear spin-splitting of CoTPP electronic states, while no magnetic response is obtained from NiTPP, as expected from the electronic configuration of the respective free molecules. We link these observations to the decoupling action of oxygen at the interface, whose effect is to enhance the molecular diffusivity and tune the electronic interaction with the substrate electronic structure.

Metal-tetraphenyl-porphyrin (M-TPP) molecules typically self-assemble forming square-like superlattices, as dictated by their shape. The dependence of the adsorption properties on the central atom is systematically studied for Co-, Ni-, and Zn-TPP adsorbed on oxygen passivated Fe(001), namely the Fe(001)- p ( 1 × 1 ) O surface. It is found by low energy electron diffraction (LEED) and scanning tunneling microscopy (STM) that despite the weak molecule–substrate interaction, preserving many features of quasi-free molecules, the self-assembled structure switches from the ( 5 × 5 ) R 37 ° superlattice of Co-TPP and Ni-TPP to the plain ( 5 × 5 ) of Zn-TPP. Ab initio calculations based on density functional theory (DFT) are used to investigate the adsorption properties of the different molecules and the possible overlayers formed. Adsorption energies, structures, and electronic properties are reported, discussing the bonding mechanisms and the magnetic character. Only moderate energy differences are found, suggesting that subtle effects may steer the selection of the structure among overlayers with similar properties although differing substantially as for the LEED and STM experimental results.

The introduction of a two-dimensional oxide layer at the interface between an organic semiconductor and a ferromagnetic metal (spinterface) can help in tailoring the formation of spin-polarized hybridized interface states. Here, we consider the case of a Cr 4 O 5 monolayer at the C 60 / Fe ( 001 ) interface, which is already known to feature the occurrence of spin-polarized states in the fullerene molecules. In this work, we employ scanning tunneling microscopy/spectroscopy and photoemission spectroscopy to show that the C 60 / Cr 4 O 5 / Fe ( 001 ) spinterface is characterized by the formation of a well-ordered fullerene monolayer and of strongly hybridized interface states. These experimental results are discussed in terms of state-of-the-art ab initio calculations of the structural, electronic, and magnetic properties at the interface.