Gate-Controlled Supercurrent in Epitaxial Al/InAs Nanowires.

Gate-controlled supercurrent (GCS) in superconducting nanobridges has recently attracted attention as a means to create superconducting switches. Despite the clear advantages for applications, the microscopic mechanism of this effect is still under debate. In this work, we realize GCS for the first time in a highly crystalline superconductor epitaxially grown on an InAs nanowire. We show that the supercurrent in the epitaxial Al layer can be switched to the normal state by applying ≃±23 V on a bottom gate insulated from the nanowire by a crystalline hBN layer. Our extensive study of the temperature and magnetic field dependencies suggests that the electric field is unlikely to be the origin of GCS in our device. Though hot electron injection alone cannot explain our experimental findings, a very recent non-equilibrium phonons based picture is compatible with most of our results.

Andreev Molecule in Parallel InAs Nanowires.

Coupling individual atoms fundamentally changes the state of matter: electrons bound to atomic cores become delocalized turning an insulating state to a metallic one. A chain of atoms could lead to more exotic states if the tunneling takes place via the superconducting vacuum and can induce topologically protected excitations like Majorana or parafermions. Although coupling a single atom to a superconductor is well studied, the hybridization of two sites with individual tunability was not reported yet. The peculiar vacuum of the Bardeen-Cooper-Schrieffer (BCS) condensate opens the way to annihilate or generate two electrons from the bulk resulting in a so-called Andreev molecular state. By employing parallel nanowires with an Al shell, two artificial atoms were created at a minimal distance with an epitaxial superconducting link between. Hybridization via the BCS vacuum was observed and the spectrum of an Andreev molecule as a function of level positions was explored for the first time.

Comparative Study of Carbon Nanosphere and Carbon Nanopowder on Viscosity and Thermal Conductivity of Nanofluids.

A comparative research on stability, viscosity (µ), and thermal conductivity (k) of carbon nanosphere (CNS) and carbon nanopowder (CNP) nanofluids was performed. CNS was synthesized by the hydrothermal method, while CNP was provided by the manufacturer. Stable nanofluids at high concentrations 0.5, 1.0, and 1.5 vol% were prepared successfully. The properties of CNS and CNP nanoparticles were analyzed with Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), specific surface area (SBET), X-ray powder diffraction (XRD), thermogravimetry/differential thermal analysis (TG/DTA), and energy dispersive X-ray analysis (EDX). The CNP nanofluids have the highest k enhancement of 10.61% for 1.5 vol% concentration compared to the base fluid, while the CNS does not make the thermal conductivity of nanofluids (knf) significantly higher. The studied nanofluids were Newtonian. The relative µ of CNS and CNP nanofluids was 1.04 and 1.07 at 0.5 vol% concentration and 30 °C. These results can be explained by the different sizes and crystallinity of the used nanoparticles.

A Novel Experimental Study on the Rheological Properties and Thermal Conductivity of Halloysite Nanofluids.

Nanofluids obtained from halloysite and de-ionized water (DI) were prepared by using surfactants and changing pH for heat-transfer applications. The halloysite nanotubes (HNTs) nanofluids were studied for several volume fractions (0.5, 1.0, and 1.5 vol%) and temperatures (20, 30, 40, 50, and 60 °C). The properties of HNTs were studied with a scanning electron microscope (SEM), energy-dispersive X-ray analysis (EDX), Fourier-transform infrared (FT-IR) spectroscopy, X-ray powder diffraction (XRD), Raman spectroscopy and thermogravimetry/differential thermal analysis (TG/DTA). The stability of the nanofluids was proven by zeta potentials measurements and visual observation. With surfactants, the HNT nanofluids had the highest thermal conductivity increment of 18.30% for 1.5 vol% concentration in comparison with the base fluid. The thermal conductivity enhancement of nanofluids containing surfactant was slightly higher than nanofluids with pH = 12. The prepared nanofluids were Newtonian. The viscosity enhancements of the nanofluid were 11% and 12.8% at 30 °C for 0.5% volume concentration with surfactants and at pH = 12, respectively. Empirical correlations of viscosity and thermal conductivity for these nanofluids were proposed for practical applications.

Electrically Controlled Spin Injection from Giant Rashba Spin-Orbit Conductor BiTeBr.

Ferromagnetic materials are the widely used source of spin-polarized electrons in spintronic devices, which are controlled by external magnetic fields or spin-transfer torque methods. However, with increasing demand for smaller and faster spintronic components utilization of spin-orbit phenomena provides promising alternatives. New materials with unique spin textures are highly desirable since all-electric creation and control of spin polarization is expected where the strength, as well as an arbitrary orientation of the polarization, can be defined without the use of a magnetic field. In this work, we use a novel spin-orbit crystal BiTeBr for this purpose. Because of its giant Rashba spin splitting, bulk spin polarization is created at room temperature by an electric current. Integrating BiTeBr crystal into graphene-based spin valve devices, we demonstrate for the first time that it acts as a current-controlled spin injector, opening new avenues for future spintronic applications in integrated circuits.

Hydrothermal Synthesis and Gas Sensing of Monoclinic MoO3 Nanosheets.

Effects of different reaction parameters in the hydrothermal synthesis of molybdenum oxides (MoO3) were investigated and monoclinic (ß-) MoO3 was prepared hydrothermally for the first time. Various temperatures (90/210 °C, and as a novelty 240 °C) and durations (3/6 h) were used. At 240 °C, cetyltrimethylammonium bromide (CTAB) and CrCl3 additives were also tested. Both the reaction temperatures and durations played a significant role in the formation of the products. At 90 °C, h-MoO3 was obtained, while at 240 °C the orthorhombic (α-) MoO3 formed with hexagonal rod-like and nanofibrous morphology, respectively. The phase transformation between these two phases was observed at 210 °C. At this temperature, the 3 h reaction time resulted in the mixture of h- and α-MoO3, but 6 h led to pure α-MoO3. With CTAB the product was bare o-MoO3, however, when CrCl3 was applied, pure metastable m-MoO3 formed with the well-crystallized nanosheet morphology. The gas sensing of the MoO3 polymorphs was tested to H2, which was the first such gas sensing study in the case of m-WO3. Monoclinic MoO3 was found to be more sensitive in H2 sensing than o-MoO3. This initial gas sensing study indicates that m-MoO3 has promising gas sensing properties and this MoO3 polymorph is promising to be studied in detail in the future.

Effect of pH in the Hydrothermal Preparation of Bi2WO6 Nanostructures.

In this study, Bi2WO6 was prepared by the hydrothermal method. The effects of reaction temperature (150/170/200 °C) and reaction time (6/12/24 h) were investigated. The role of strongly acidic pH (1 >) and the full range between 0.3 and 13.5 were studied first. Every sample was studied by XRD and SEM; furthermore, the Bi2WO6 samples prepared at different temperatures were examined in detail by EDX and TEM, as well as FT-IR, Raman and UV-vis spectroscopies. It was found that changing the temperature and time slightly influenced the crystallinity and morphology of the products. The most crystallized product formed at 200 °C, 24 h. The pure, sheet-like Bi2WO6, prepared at 200 °C, 24 h, and 0.3 pH, gradually transformed into a mixture of Bi2WO6 and Bi3.84W0.16O6.24 with increasing pH. The nanosheets turned into a morphology of mixed shapes in the acidic range (fibers, sheets, irregular forms), and became homogenous cube- and octahedral-like shapes in the alkaline range. Their band gaps were calculated and were found to vary between 2.66 and 2.59 eV as the temperature increased. The specific surface area measurements revealed that reducing the temperature favors the formation of a larger surface area (35.8/26/21.6 m2/g belonging to 150/170/200 °C, respectively).

Effect of Different Anions Upon the WO3 Morphology and Structure.

In this study the effects of various anions (SO2-4, ClO-4 and PO3-4) were investigated on the hydrothermal treatment of WO3 from Na2WO4 and HCl at 180 and 200 °C. The products were analyzed by XRD and SEM. With the usage of SO2-4 the obtained product was hexagonal (h-) WO3 in the form of nanorods at both temperatures. Applying ClO-4 resulted in a mixture of WO3·0.33H2O and small amount of m-WO3 at 180 °C and pure WO3·0.33H2O at 200 °C. The morphology was consisted of cuboid shapes arranged into spherical structures at 180 °C and longitudinal ones at 200 °C. By the application of PO3-4 no product formed at either temperature. Using the combination of SO2-4, and ClO-4 the product was h-WO3 at both 180 and 200 °C with rod-like crystals; thus, the effect of ClO-4 was overdominated by the SO2-4ions. Utilization of PO3-4 together with SO2-4, and/or ClO-4 resulted again in no product, meaning that adding PO3-4 to the reaction mixture completely blocks the hydrothermal formation of solid products by forming water soluble phosphotungstic acids.

Contacting ZnO Individual Crystal Facets by Direct Write Lithography.

Many advanced electronic devices take advantage of properties developed at the surface facets of grown crystals with submicrometer dimensions. Electrical contacts to individual crystal facets can make possible the investigations of facet-dependent properties such as piezoelectricity in ZnO or III-nitride crystals having noncentrosymmetric structure. However, a lithography-based method for developing contacts to individual crystal facets with submicrometer size has not yet been demonstrated. In this report we study the use of electron beam-induced deposition (EBID), a direct write lithography method, for contacting individual facets of ZnO pillars within an electron microscope. Correlating structural and in situ deposition and electrical data, we examine proximity effects during the EBID and evaluate the process against obtaining electrically insulated contact lines on neighboring and diametrically opposite ZnO facets. Parameters such as incident beam energy geometry and size of the facets were investigated with the view of minimizing unwanted proximity broadening effects. Additionally, we show that the EBID direct write method has the required flexibility, resolution, and minimized proximity deposition for creating prototype devices. The devices were used to observe facet-dependent effects induced by mechanical stress on single ZnO pillar structures.