Electrical transport in ion beam created InAs nanospikes

Ion beam irradiation has previously been demonstrated as a method for creating nanowire-like semiconductor nanostructures, but no previous studies have reported on the electrical properties of those structures. In this work we describe the creation and in situ transmission electron microscopy electrical characterization of nanoscale InAs spike structures on both InAs and InP substrates fabricated using a focused ion beam erosion method. Those InAs ‘nanospikes’ are found to possess internal structures with varying amounts of ion damaged and single crystalline material. Nanospike electrical behavior is analyzed with respect to model electronic structures and is similar to cases of barrier limited conduction in nanowires. The different electrical responses of each nanospike are found to be the result of variation in their structure, with the conductivity of InAs nanospikes formed on InAs substrates found to increase with the degree of nanospike core crystallinity. The conductivity of InAs nanospikes formed on InP substrates does not show a dependence on core crystallinity, and may be controlled by the other internal barriers to conduction inherent in that system.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/98603/1/0957-4484_23_31_315301.pd

Benzene at 1GHz. Magnetic field-induced fine structure

The deuterium NMR spectrum of benzene-d6 in a high field spectrometer (1 GHz protons) exhibits a magnetic field-induced deuterium quadrupolar splitting ??. The magnitude of ?? observed for the central resonance is smaller than that observed for the 13C satellite doublets ???. This difference, ?(??) = ??? ? ??, is due to unresolved fine structure contributions to the respective resonances. We determine the origins of and simulate this difference, and report pulse sequences that exploit the connectivity of the peaks in the 13C and 2H spectra to determine the relative signs of the indirect coupling, JCD, and ??. The positive sign found for ?? is consonant with the magnetic field biasing of an isolated benzene molecule—the magnetic energy of the aromatic ring is lowest for configurations where the C6 axis is normal to the field. In the neat liquid the magnitude of ?? is decreased by the pair correlations in this prototypical molecular liquid

Dielectric properties of liquid crystalline dimer mixtures exhibiting the nematic and twist-bend nematic phases

A detailed investigation of the thermal and dielectric properties of a series of binary mixtures exhibiting the nematic ( N ) and twist-bend nematic ( N TB ) liquid crystal phases is presented. The mixtures consist of an achiral, dimeric liquid crystal CB7CB, which forms the nematic and twist-bend nematic phases, and a calamitic liquid crystal 5CB, which shows the nematic phase. As the concentration of the calamitic liquid crystal is increased, the transition temperatures decrease linearly, and the width of the nematic phase increases. The enthalpies of phase transitions obtained from DSC measurements show that on increasing the concentration of 5CB in the binary mixtures, the enthalpy associated with the N − N TB phase transitions reduces considerably compared to a clear first-order N − N TB transition in pure CB7CB. The real and imaginary parts of the dielectric permittivity are measured as a function of frequency from 100 Hz to 2 MHz in the nematic and twist-bend nematic phases in planar and homeotropic devices. A significant decrease in the average dielectric permittivity as a function of temperature for mixtures forming the N TB phase is observed. Measurements of the imaginary part of the dielectric permittivity show a relaxation peak in the measured frequency window for all of the mixtures exhibiting the N TB phase. The activation energy associated with this relaxation process is calculated and is shown to remain constant irrespective of the composition of the mixtures

Modern microwave methods in solid state inorganic materials chemistry: from fundamentals to manufacturing

No abstract available

Reactive synthesis of Ti-Al intermetallics during microwave heating in an E-field maximum

The time-resolved X-ray diffraction synchrotron radiation technique was used in combination with E-field microwave heating to study in situ the kinetics of intermetallic phase formation in the Ti-Al system. The reaction of Ti with Al is triggered by the melting and spreading of Al onto the surface of Ti particles. The tetragonal TiAl 3 phase is the primary reaction product, formed by instantaneous nucleation at the interface between the unreacted Ti cores and the Al melt. The growth of TiAl 3 layers is diffusion-controlled. These preliminary results demonstrate that microwave heating can be used to rapidly synthesise intermetallic phases from high-purity elemental powders. © 2010 Elsevier B.V. All rights reserved.This work has been supported by the Swiss National Science Foundation (Grant 20PA21E-129193).Vaucher, S.; Stir, M.; Ishizaki, K.; Catalá Civera, JM.; Nicula, R. (2011). Reactive synthesis of Ti-Al intermetallics during microwave heating in an E-field maximum. Thermochimica Acta. 522(1):151-154. doi:10.1016/j.tca.2010.11.026S151154522

Benzene at 1GHz. Magnetic field-induced fine structure

International audienceThe deuterium NMR spectrum of benzene-d(6) in a high field spectrometer (1 GHz protons) exhibits a magnetic field-induced deuterium quadrupolar splitting Delta v. The magnitude of Delta v observed for the central resonance is smaller than that observed for the C-13 satellite doublets Delta v'. This difference, Delta(Delta v) Delta v' - Delta v, is due to unresolved fine structure contributions to the respective resonances. We determine the origins of and simulate this difference, and report pulse sequences that exploit the connectivity of the peaks in the C-13 and H-2 spectra to determine the relative signs of the indirect coupling, J(CD), and Delta v. The positive sign found for Delta v is consonant with the magnetic field biasing of an isolated benzene molecule-the magnetic energy of the aromatic ring is lowest for configurations where the C-6 axis is normal to the field. In the neat liquid the magnitude of Delta v is decreased by the pair correlations in this prototypical molecular liquid

Millennials in the Workplace: A Communication Perspective on Millennials’ Organizational Relationships and Performance

Stereotypes about Millennials, born between 1979 and 1994, depict them as self-centered, unmotivated, disrespectful, and disloyal, contributing to widespread concern about how communication with Millennials will affect organizations and how they will develop relationships with other organizational members. We review these purported characteristics, as well as Millennials’ more positive qualities—they work well in teams, are motivated to have an impact on their organizations, favor open and frequent communication with their supervisors, and are at ease with communication technologies. We discuss Millennials’ communicated values and expectations and their potential effect on coworkers, as well as how workplace interaction may change Millennials

NMR of quadrupole noble gases in liquid crystals

Abstract NMR spectroscopy of quadrupolar noble gases, 21Ne (spin 3/2), 83Kr (9/2), 131Xe (3/2), dissolved in thermotropic liquid crystals enables the derivation of versatile information about the physical properties of the materials. The spectra display fine structures, triplets and nonets, which reveal quadrupole couplings. These, in turn, can be used in the determination of electric field gradients (EFG), orientational order parameters, and tilt angles. Comparison of 129Xe and 131Xe chemical shifts reveals second-order quadrupole shifts (SOQS) in circumstances where the ratio of quadrupole coupling and magnetic flux density is suitable. The 131Xe SOQS is shown to distinguish between uniaxial and biaxial nematic phases. Both 83Kr and 131Xe NMR spectra may display asymmetry around the central transition because of the SOQS, which can be used to identify biaxiality in nematic phases. As a curiosity, the effect of possible hexadecapole coupling on the 83Kr NMR transitions of krypton in liquid crystals is discussed