Ti-doped BiFeO3 ceramics prepared by a mixed-oxide route were structurally characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM), giving evidence of the formation of an inner structure at the nanometric scale. The observed nanograins are separated by Ti-rich areas that originate due to the tendency of the titanium dopant to segregate from the perovskite lattice. Such a peculiar nanostructure is responsible for the changes produced in both the electrical and the magnetic properties of BiFeO3 upon titanium doping: the Ti-rich interfaces act as resistive layers that increase the direct-current (dc) resistivity of the material, while the existence of structural domains in the scale of tens of nanometers causes a ferrimagnetic-like behavior with a huge coercive field (on the order of 20 kOe), even at room temperature.

We present very low-temperature scanning tunneling microscopy (STM) experiments on single-crystalline samples of the superconductor β-Bi 2 Pd. We find a single superconducting gap from the zero-field tunneling conductance. However, the magnetic field dependence of the intervortex tunneling conductance is higher than the one expected in a single-gap superconductor. Such an increase in the intervortex tunneling conductance has been found in superconductors with multiple superconducting gaps. We also find that the hexagonal vortex lattice is locked to the square atomic lattice as expected in crystalline superconductors with anisotropic Fermi surfaces. Moreover, we compare the upper critical field H c2 (T ) obtained in our sample with previous measurements and find that H c2 (T ) does not increase by reducing the mean free path. We fit H c2 (T ) and show that multiband Fermi surface is needed to explain the observed behavior. We propose that β-Bi 2 Pd is a single-gap multiband superconductor. We anticipate that single-gap superconductivity might often occur in compounds with anisotropic multiband Fermi surfaces.

The peculiar features of domain walls observed in ferroelectrics make them promising active elements for next-generation non-volatile memories, logic gates and energy-harvesting devices. Although extensive research activity has been devoted recently to making full use of this technological potential, concrete realizations of working nanodevices exploiting these functional properties are yet to be demonstrated. Here, we fabricate a multiferroic tunnel junction based on ferromagnetic LaSrMnO electrodes separated by an ultrathin ferroelectric BaTiO tunnel barrier, where a head-to-head domain wall is constrained. An electron gas stabilized by oxygen vacancies is confined within the domain wall, displaying discrete quantum-well energy levels. These states assist resonant electron tunnelling processes across the barrier, leading to strong quantum oscillations of the electrical conductance.

SnSe has been prepared by arc-melting, as mechanically robust pellets, consisting of highly oriented polycrystals. This material has been characterized by neutron powder diffraction (NPD), scanning electron microscopy, and transport measurements. A microscopic analysis from NPD data demonstrates a quite perfect stoichiometry SnSe0.98(2) and a fair amount of anharmonicity of the chemical bonds. The Seebeck coefficient reaches a record maximum value of 668 μV K−1 at 380 K; simultaneously, this highly oriented sample exhibits an extremely low thermal conductivity lower than 0.1 W m−1 K−1 around room temperature, which are two of the main ingredients of good thermoelectric materials. These excellent features exceed the reported values for this semiconducting compound in single crystalline form in the moderate-temperatures region and highlight its possibilities as a potential thermoelectric material.

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Graphene functionalization with organics is expected to be an important step for the development of graphene-based materials with tailored electronic properties. However, its high chemical inertness makes difficult a controlled and selective covalent functionalization, and most of the works performed up to the date report electrostatic molecular adsorption or unruly functionalization. We show hereafter a mechanism for promoting highly specific covalent bonding of any amino-terminated molecule and a description of the operating processes. We show, by different experimental techniques and theoretical methods, that the excess of charge at carbon dangling-bonds formed on single-atomic vacancies at the graphene surface induces enhanced reactivity towards a selective oxidation of the amino group and subsequent integration of the nitrogen within the graphene network. Remarkably, functionalized surfaces retain the electronic properties of pristine graphene. This study opens the door for development of graphene-based interfaces, as nano-bio-hybrid composites, fabrication of dielectrics, plasmonics or spintronics.

Thermoelectric materials may contribute in the near future as new alternative sources of sustainable energy. Unprecedented thermoelectric properties in p-type SnSe single crystals have been recently reported, accompanied by extremely low thermal conductivity in polycrystalline samples. In order to enhance thermoelectric efficiency through proper tuning of this material we report a full structural characterization and evaluation of the thermoelectric properties of novel Ge-doped SnSe prepared by a straightforward arc-melting method, which yields nanostructured polycrystalline samples. Ge does not dope the system in the sense of donating carriers, yet the electrical properties show a semiconductor behavior with resistivity values higher than that of the parent compound, as a consequence of nanostructuration, whereas the Seebeck coefficient is higher and thermal conductivity lower, favorable to a better ZT figure of merit.

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