A propagating Majorana mode Although Majorana fermions remain elusive as elementary particles, their solid-state analogs have been observed in hybrid semiconductor-superconductor nanowires. In a nanowire setting, the Majorana states are localized at the ends of the wire. He et al. built a two-dimensional heterostructure in which a one-dimensional Majorana mode is predicted to run along the sample edge (see the Perspective by Pribiag). The heterostructure consisted of a quantum anomalous Hall insulator (QAHI) bar contacted by a superconductor. The authors used an external magnetic field as a “knob” to tune into a regime where a Majorana mode was propagating along the edge of the QAHI bar covered by the superconductor. A signature of this propagation—half-quantized conductance—was then observed in transport experiments. Science , this issue p. 294 ; see also p. 252
Heterogeneous processes at solid/gas, liquid/gas and solid/liquid interfaces are ubiquitous in modern devices and technologies but often difficult to study quantitatively. Full characterization requires measuring the depth profiles of chemical composition and state with enhanced sensitivity to narrow interfacial regions of a few to several nm in extent over those originating from the bulk phases on either side of the interface. We show for a model system of NaOH and CsOH in an B1-nm thick hydrated layer on a-Fe 2 O 3 (haematite) that combining ambient-pressure X-ray photoelectron spectroscopy and standing-wave photoemission spectroscopy provides the spatial arrangement of the bulk and interface chemical species, as well as local potential energy variations, along the direction perpendicular to the interface with sub-nm accuracy. Standing-wave ambient-pressure photoemission spectroscopy is thus a very promising technique for measuring such important interfaces, with relevance to energy research, heterogeneous catalysis, electrochemistry, and atmospheric and environmental science.
Free-standing, interconnected metallic nanowire networks with density as low as 40 mg/cm 3 have been achieved over cm-scale areas, using electrodeposition into polycarbonate membranes that have been ion-tracked at multiple angles. Networks of interconnected magnetic nanowires further provide an exciting platform to explore 3-dimensional nanomagnetism, where their structure, topology and frustration may be used as additional degrees of freedom to tailor the materials properties. New magnetization reversal mechanisms in cobalt networks are captured by the first-order reversal curve method, which demonstrate the evolution from strong demagnetizing dipolar interactions to intersections-mediated domain wall pinning and propagation, and eventually to shape-anisotropy dominated magnetization reversal. These findings open up new possibilities for 3-dimensional integrated magnetic devices for memory, complex computation, and neuromorphics.
Nanostructured palladium foams offer exciting potential for applications in diverse fields such as catalyst, fuel cell, and particularly hydrogen storage technologies. We have fabricated palladium nanowire foams using a cross-linking and freeze-drying technique. These foams have a tunable density down to 0.1% of the bulk, and a surface area to volume ratio of up to 1,540,000:1. They exhibit highly attractive characteristics for hydrogen storage, in terms of loading capacity, rate of absorption and heat of absorption. The hydrogen absorption/desorption process is hysteretic in nature, accompanied by substantial lattice expansion/contraction as the foam converts between Pd and PdHx.Comment: 17 pages, 4 figure
A cluster deposition method was used to produce films of loosely aggregated nanoclusters (NC) of Fe core-Fe 3 O 4 shell or fully oxidized Fe 3 O 4 . Films of these NC on Si(100) or MgO(100)/Fe 3 O 4 (100) were irradiated to 10 16 Si 2+ /cm 2 near room temperature using an ion accelerator. Ion irradiation creates structural change in the NC film with corresponding chemical and magnetic changes which depend on the initial oxidation state of the cluster. Films were characterized using magnetometry (hysteresis, first order reversal curves), microscopy (transmission electron, helium ion), and x-ray diffraction. In all cases, the particle sizes increased due to ion irradiation, and when a core of Fe is present, irradiation reduces the oxide shells to lower valent Fe species. These results show that ion irradiated behavior of the nanocluster films depends strongly on the initial nanostructure and chemistry, but in general saturation magnetization decreases slightly.
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