In the majority of cases nanostructures prepared by focused electron beam induced deposition (FEBID) employing an organometallic precursor contain predominantly carbon-based ligand dissociation products. This is unfortunate with regard to using this high-resolution direct-write approach for the preparation of nanostructures for various fields, such as mesoscopic physics, micromagnetism, electronic correlations, spin-dependent transport and numerous applications. Here we present an in situ cleaning approach to obtain pure Co-FEBID nanostructures. The purification procedure lies in the exposure of heated samples to a H2 atmosphere in conjunction with the irradiation by low-energy electrons. The key finding is that the combination of annealing at 300 °C, H2 exposure and electron irradiation leads to compact, carbon- and oxygen free Co layers down to a thickness of about 20 nm starting from as-deposited Co-FEBID structures. In addition to this, in temperature-dependent electrical resistance measurements on post-processed samples we find a typical metallic behavior. In low-temperature magnetoresistance and Hall effect measurements we observe ferromagnetic behavior.

We report an experimental study of proximity effect-induced superconductivity in crystalline Cu and Co nanowires and a nanogranular Co nanowire structure in contact with a superconducting W floating electrode which we call inducer. The nanowires were grown by electrochemical deposition in heavy-ion-track etched polycarbonate templates. The nanogranular Co structure was fabricated by focused electron beam induced deposition (FEBID), while the amorphous W inducer was obtained by focused ion beam induced deposition (FIBID). For electrical resistance measurements up to three pairs of Pt voltage leads were deposited by FIBID at different distances beside the inner inducer electrode, thus allowing us to probe the proximity effect over a length of 2 − 12 µm. Relative R(T ) drops of the same order of magnitude have been observed for the Co and Cu nanowires when sweeping the temperature below 5.2 K (Tc of the FIBID-deposited W inducer). By contrast, relative R(T ) drops were found to be an order of magnitude smaller for the nanogranular Co nanowire structure. Our analysis of the resistance data shows that the superconducting proximity length in crystalline Cu and Co is about 1 µm at low temperatures, attesting to a long-range proximity effect in the case of ferromagnetic Co. Moreover, this long-range proximity effect has been revealed to be insusceptible to magnetic fields up to 11 T, which is indicative of spin-triplet pairing. At the same time, in the nanogranular Co structure proximity-induced superconductivity is strongly suppressed due to the dominating Cooper pair scattering caused by the intrinsic microstructure of the FEBID deposit.

SummaryControlling magnetic properties on the nanometer-scale is essential for basic research in micro-magnetism and spin-dependent transport, as well as for various applications such as magnetic recording, imaging and sensing. This has been accomplished to a very high degree by means of layered heterostructures in the vertical dimension. Here we present a complementary approach that allows for a controlled tuning of the magnetic properties of Co/Pt heterostructures on the lateral mesoscale. By means of in situ post-processing of Pt- and Co-based nano-stripes prepared by focused electron beam induced deposition (FEBID) we are able to locally tune their coercive field and remanent magnetization. Whereas single Co-FEBID nano-stripes show no hysteresis, we find hard-magnetic behavior for post-processed Co/Pt nano-stripes with coercive fields up to 850 Oe. We attribute the observed effects to the locally controlled formation of the CoPt L10 phase, whose presence has been revealed by transmission electron microscopy.

We report an experimental study of proximity effect-induced superconductivity in crystalline Cu and Co nanowires and a nanogranular Co nanowire structure in contact with a superconducting W-based floating electrode (inducer). For electrical resistance measurements up to three pairs of Pt-based voltage leads were attached at different distances beside the inner inducer electrode, thus allowing us to probe the proximity effect over a length of 2–12 μm. Up to 30% resistance drops with respect to the normal-state value have been observed for the crystalline Co and Cu nanowires when sweeping the temperature below Tc of the inducer (5.2 K). By contrast, relative R(T) drops were found to be an order of magnitude smaller for the nanogranular Co nanowire structure. Our analysis of the resistance data shows that the superconducting proximity length in crystalline Cu and Co is about 1 μm at 2.4 K, attesting to a long-range proximity effect in the Co nanowire. Moreover, this long-range proximity effect is insusceptible to magnetic fields up to 11 T, which is indicative of spin-triplet pairing. At the same time, proximity-induced superconductivity in the nanogranular Co nanowire is strongly suppressed due to the dominating Cooper pair scattering caused by its intrinsic microstructure.

Controlling magnetic properties on the nm-scale is essential for basic research in micro-magnetism and spin-dependent transport, as well as for various applications such as magnetic recording, imaging and sensing. This has been accomplished to a very high degree by means of layered heterostructures in the vertical dimension. Here we present a complementary approach that allows for a controlled tuning of the magnetic properties of Co/Pt heterostructures on the lateral mesoscale. By means of in-situ post-processing of Pt-and Co-based nano-stripes prepared by focused electron beam induced deposition (FEBID) we are able to locally tune their coercive field and remanent magnetization. Whereas single Co-FEBID nano-stripes show no hysteresis, we find hard-magnetic behavior for postprocessed Co/Pt nano-stripes with coercive fields up to 850 Oe. We attribute the observed effects to the locally controlled formation of the CoPt L10 phase, whose presence has been revealed by transmission electron microscopy.