ABSTRACT
The magnetic properties and the atomic scale morphology of bimetallic two-dimensional nanoislands, epitaxially grown on fcc(111) metal surfaces, have been studied by means of Magneto-Optical Kerr Effect and Scanning Tunneling Microscopy. We investigate the effect on blocking temperature of one-dimensional interlines appearing in core-shell structures, of two-dimensional interfaces created by capping, and of random alloying. The islands are grown on Pt(111) and contain a Co-core, surrounded by Ag, Rh, and Pd shells, or capped by Pd. The largest effect is obtained by Pd capping, increasing the blocking temperature by a factor of three compared to pure Co islands. In addition, for Co-core Fe-shell and Co-core FexCo1-x-shell islands, self-assembled into well ordered superlattices on Au(11,12,12) vicinal surfaces, we find a strong enhancement of the blocking temperature compared to pure Co islands of the same size. These ultra-high-density (15 Tdots/in2) superlattices of CoFe nanodots, only 500 atoms in size, have blocking temperature exceeding 100 K. Our findings open new possibilities to tailor the magnetic properties of nanoislands.
ABSTRACT
Non-collinear magnetization textures provide a route to novel device concepts in spintronics. These applications require laterally confined non-collinear magnets (NCM). A crucial aspect for potential applications is how the spatial proximity between the NCM and vacuum or another material impacts the magnetization texture on the nanoscale. We focus on a prototypical exchange-driven NCM given by the helical spin order of bilayer Fe on Cu(111). Spin-polarized scanning tunnelling spectroscopy and density functional theory reveal a nanosize- and proximity-driven modification of the electronic and magnetic structure of the NCM in interfacial contact with a ferromagnet or with vacuum. An intriguing non-collinearity between the local magnetization in the sample and the electronic magnetization probed above its surface results. It is a direct consequence of the spinor nature of electronic states in NCM. Our findings provide a possible route for advanced control of nanoscale spin textures by confinement.
