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A proposal for an electron-beam device that can act as an efficient spin-polarization filter has been recently put forward (Karimi et al 2012 Phys. Rev. Lett. 108 044801). It is based on combining the recently developed diffraction technology for imposing orbital angular momentum to the beam with a multipolar Wien filter inducing a sort of artificial non-relativistic spin–orbit coupling. Here we reconsider the proposed device with a fully quantum-mechanical simulation of the electron-beam propagation, based on the well-established multi-slice method, supplemented with a Pauli term for taking into account the spin degree of freedom. Using this upgraded numerical tool, we study the feasibility and practical limitations of the proposed method for spin polarizing a free electron beam.

High-dimensional encoding schemes have emerged as a novel way to perform quantum information tasks. For high dimensionality, temporal and transverse spatial modes of photons are the two paradigmatic degrees of freedom commonly used in such experiments. Nevertheless, general devices for multi-outcome measurements are still needed to take full advantage of the high-dimensional nature of encoding schemes. We propose a general full-field mode sorting scheme consisting of only up to two optimized phase elements based on evolutionary algorithms that allows for joint sorting of azimuthal and radial modes. We further study the performance of our scheme through simulations in the context of high-dimensional quantum cryptography, where sorting in different mutually unbiased bases and high-fidelity measurement schemes are crucial. [ABSTRACT FROM AUTHOR]

Ceria nanoparticles (NPs) are fundamental in heterogeneous catalysis because of their ability to store or release oxygen depending on the ambient conditions. Their oxygen storage capacity is strictly related to the exposed planes, crystallinity, density and distribution of defects. In this work a study of ceria NPs produced with a ligand-free, physical synthesis method is presented. The NP films were grown by a magnetron sputtering based gas aggregation source and studied by high resolution- and scanning-transmission electron microscopy and x-ray photoelectron spectroscopy. In particular, the influence of the oxidation procedure on the NP reducibility has been investigated. The different reducibility has been correlated to the exposed planes, crystallinity and density and distribution of structural defects. The results obtained in this work represent a basis to obtain cerium oxide NP with desired oxygen transport properties. [ABSTRACT FROM AUTHOR]

Films of magnetic Ni@NiO core–shell nanoparticles (NPs, core diameter d ≅ 12 nm, nominal shell thickness variable between 0 and 6.5 nm) obtained with sequential layer deposition were investigated, to gain insight into the relationships between shell thickness/morphology, core–shell interface, and magnetic properties. Different values of NiO shell thickness ts could be obtained while keeping the Ni core size fixed, at variance with conventional oxidation procedures where the oxide shell is grown at the expense of the core. Chemical composition, morphology of the as-produced samples and structural features of the Ni/NiO interface were investigated with x-ray photoelectron spectroscopy and microscopy (scanning electron microscopy, transmission electron microscopy) techniques, and related with results from magnetic measurements obtained with a superconducting quantum interference device. The effect of the shell thickness on the magnetic properties could be studied. The exchange bias (EB) field Hbias is small and almost constant for ts up to 1.6 nm; then it rapidly grows, with no sign of saturation. This behavior is clearly related to the morphology of the top NiO layer, and is mostly due to the thickness dependence of the NiO anisotropy constant. The ability to tune the EB effect by varying the thickness of the last NiO layer represents a step towards the rational design and synthesis of core–shell NPs with desired magnetic properties. [ABSTRACT FROM AUTHOR]

We report the Au-assisted chemical beam epitaxy growth of defect-free zincblende InSb nanowires. The grown InSb segments are the upper sections of InAs/InSb heterostructures on InAs(111)B substrates. We show, through HRTEM analysis, that zincblende InSb can be grown without any crystal defects such as stacking faults or twinning planes. Strain-map analysis demonstrates that the InSb segment is nearly relaxed within a few nanometers from the interface. By post-growth studies we have found that the catalyst particle composition is AuIn2, and it can be varied to a AuIn alloy by cooling down the samples under TDMASb flux. [ABSTRACT FROM AUTHOR]

Self-assembled GaAs nanowires have been grown on Si by molecular beam epitaxy without the use of any outside metal catalyst. The growth occurs on Si facets obtained by the cleavage of Si(100) substrates. The growth has been obtained with or without Ga pre-deposition. In both cases two kinds of nanowires have been obtained. The wires of the first type clearly present a Ga droplet at their free end and have a lattice structure that is wurtzite for wide regions beneath the Ga droplet. The second type, in contrast, ends with pyramidally shaped GaAs and has a crystal lattice that is mainly zincblende with only a few and small wurtzite regions, if any. The Ga-ended nanowires are longer than the others and thinner on average. The experimental findings suggest that the two types of nanowires grow after different growth processes. [ABSTRACT FROM AUTHOR]