RESUMO
3D topological insulators (TI) host surface carriers with extremely high mobility. However, their transport properties are typically dominated by bulk carriers that outnumber the surface carriers by orders of magnitude. A strategy is herein presented to overcome the problem of bulk carrier domination by using 3D TI nanoparticles, which are compacted by hot pressing to macroscopic nanograined bulk samples. Bi2 Te3 nanoparticles well known for their excellent thermoelectric and 3D TI properties serve as the model system. As key enabler for this approach, a specific synthesis is applied that creates nanoparticles with a low level of impurities and surface contamination. The compacted nanograined bulk contains a high number of interfaces and grain boundaries. Here it is shown that these samples exhibit metallic-like electrical transport properties and a distinct weak antilocalization. A downward trend in the electrical resistivity at temperatures below 5 K is attributed to an increase in the coherence length by applying the Hikami-Larkin-Nagaoka model. THz time-domain spectroscopy reveals a dominance of the surface transport at low frequencies with a mobility of above 103 cm2 V-1 s-1 even at room temperature. These findings clearly demonstrate that nanograined bulk Bi2 Te3 features surface carrier properties that are of importance for technical applications.
RESUMO
The synthesis of phase-pure ternary solutions of tetradymite-type materials (Bix Sb1-x )2 Te3 (x=0.25; 0.50; 0.75) in an ionic liquid approach has been carried out. The nanoparticles are characterized by means of energy-dispersive X-ray spectroscopy (EDX), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and transmission electron microscopy. In addition, the role of different processing approaches on the thermoelectric properties - Seebeck coefficient as well as electrical and thermal conductivity - is demonstrated.
RESUMO
In order to reverse the magnetization of small ferromagnetic particles it is necessary to overcome an energy barrier, which is mainly defined by the magnetic anisotropy. Usual reversal stimuli include the application of static or time-dependent external magnetic fields, thermal activation, spin transfer torque, or combinations thereof. Here, we report on repeated, quasi-periodic magnetization reversal in single-domain particles that are exposed to a constant magnetic field perpendicular to the magnet's easy axis. The continuous sequence of reversals is induced by torsional oscillations of the magnet's anisotropy landscape, which are caused by angular oscillations of the magnet's body. In our experiments, a nickel nanowire constitutes both a mechanical resonator and a nanomagnetic sample with uniaxial anisotropy. We measure the transient flexural vibration behavior by electron beam based methods and find strong signatures of periodic magnetization switching between two magnetic states of the nanowire. Our system can be modeled as a driven damped harmonic oscillator under the influence of switchable magnetostatic interactions.
RESUMO
We demonstrate a new approach to fabricate highly ordered arrays of nanoscopic palladium dots and wires using switchable block copolymer thin films. The surface-reconstructed block copolymer templates were directly deposited with palladium nanoparticles from a simple aqueous solution. The preferential interaction of the nanoparticles with one of the blocks is mainly responsible for the lateral arrangement of the nanoparticles inside the pores of the templates in addition to the capillary forces. A subsequent stabilization by UV-irradiation followed by pyrolysis in air at 450 degrees C removes the polymer to produce highly ordered metallic nanostructures. We extended this approach to micellar films to obtain metallic nanostructures. This method is highly versatile as the procedure used here is simple, eco-friendly and provides a simple approach to fabricate a broad range of nanoscaled architectures with tunable lateral spacing, and can be extended to systems with even smaller dimensions.
