Tuning magnetic fingerprints of FeNi nanowire arrays by varying length and diameter

Magnetic nanowires (NWs) electrodeposited into solid templates are of high interest due to their tunable properties which are required for magnetic recording media and spintronic devices. Here, highly ordered arrays of FeNi NWs with varied lengths (ranging from 2.5 to 12 μm) and diameters (between 45 and 75 nm) were fabricated into anodic aluminum oxide templates using a pulsed ac electrodeposition technique. X-ray diffraction patterns along with energy dispersive spectroscopy indicated the formation of Fe₇₀Ni₃₀ NWs with fcc and bcc alloy phases, being highly textured along the bcc [110] direction. Magnetic properties were studied by hysteresis loop measurements at room temperature and they showed reductions in coercivity and squareness values by increasing length and diameter. Further, magnetic fingerprints of the NWs were characterized using the first-order reversal curve (FORC) analysis. FORC measurements revealed that, with increasing length and diameter from 2.5 to 10 μm and 45–55 nm, respectively, besides an increase in inter-wire magnetostatic interactions, a transition from a single domain (SD) state to a pseudo SD state occurred. Moreover, a multi-domain (MD) state was found for the longest length and diameter. While the irreversible magnetization component of the SD NWs was approximately 100%, the reversible component of MD NWs increased up to 20%.     

Strain localisation in granular media

This paper discusses strain localisation in granular media by presenting experimental, full-field analysis of mechanical tests on sand, both at a continuum level, as well as at the grain scale. At the continuum level, the development of structures of localised strain can be studied. Even at this scale, the characteristic size of the phenomena observed is in the order of a few grains. In the second part of this paper, therefore, the development of shear bands within specimen of different sands is studied at the level of the individual grains, measuring grains kinematics with x-ray tomography. The link between grain angularity and grain rotation within shear bands is shown, allowing a grain-scale explanation of the difference in macroscopic residual stresses for materials with different grain shapes. Finally, rarely described precursors of localisation, emerging well before the stress peak are observed and commented.     

Effect of Surface Passivation in Spinel Slurry Toward Hydrolysis: Neutron Scattering and Rheological Studies

Aqueous colloidal forming of magnesium aluminate (MgAl₂O₄) spinel offers much potential for various applications; however, these advantages are generally offset by the basic nature of the powder and its affinity for hydrolysis. Hydrolysis in the presence of water generally imparts surface chemical changes resulting in the degradation of colloidal stability. In the present study, spinel powders were subjected to thermally assisted surface passivation and evaluated for the effectiveness of preventing hydrolysis through quasielastic neutron scattering (QENS) technique and correlated with rheological measurements. In order to evaluate the extent of hydrolysis, spinel slurries prepared with (SP) and without surface passivation (WSP) were studied by rheological and QENS measurements at regular intervals of time. While WSP slurry exhibited a steep enhancement in viscosity from 1.02 to 19.4 Pa · s and fraction of the elastic intensity from 0.20 to 0.38 for 96 and 200 hours, respectively, a negligible change in viscosity for SP slurries from 0.313 to 0.345 Pa · s and fraction of the elastic intensity from 0.16 to 0.17 for the similar period confirmed the inhibition of hydrolysis, revealing change in surface chemistry due to hydrolysis. Microscopic details as obtained from neutron scattering data revealed that dynamical behavior of water molecules in both the slurries could be described very well by the Singwi–Sjolander model of jump diffusion. Further analysis showed lower diffusivity ～1.82 × 10^?5 cm²/sec and higher residence time ～6.39 ps for WSP slurry in comparison with 2.16 × 10^?5 cm²/sec and 5.80 ps, complimenting the inhibition of hydrolysis in case of SP slurry.     

Accurate thermodynamic characterization of a synthetic coal mine methane mixture

In the last few years, coal mine methane (CMM) has gained significance as a potential non-conventional gas fuel. The progressive depletion of common fossil fuels reserves and, on the other hand, the positive estimates of CMM resources as a by-product of mining promote this fuel gas as a promising alternative fuel. The increasing importance of its exploitation makes it necessary to check the capability of the present-day models and equations of state for natural gas to predict the thermophysical properties of gases with a considerably different composition, like CMM. In this work, accurate density measurements of a synthetic CMM mixture are reported in the temperature range from (250 to 400) K and pressures up to 15 MPa, as part of the research project EMRP ENG01 of the European Metrology Research Program for the characterization of non-conventional energy gases. Experimental data were compared with the densities calculated with the GERG-2008 equation of state. Relative deviations between experimental and estimated densities were within a 0.2% band at temperatures above 275 K, while data at 250 K as well as at 275 K and pressures above 10 MPa showed higher deviations.     

Ultrafast Two‐Dimensional NMR Relaxometry for Investigating Molecular Processes in Real Time

Nuclear spin–lattice (T₁) and spin–spin (T₂) relaxation times provide versatile information about the dynamics and structure of substances, such as proteins, polymers, porous media, and so forth. Multidimensional experiments increase the information content and resolution of NMR relaxometry, but they also multiply the measurement time. To overcome this issue, we present an efficient strategy for a single‐scan measurement of a 2D T₁–T₂ correlation map. The method shortens the experimental time by one to three orders of magnitude as compared to the conventional method, offering an unprecedented opportunity to study molecular processes in real‐time. We demonstrate that, despite the tremendous speed‐up, the T₁–T₂ correlation maps determined by the single‐scan method are in good agreement with the maps measured by the conventional method. The concept of the single‐scan T₁–T₂ correlation experiment is applicable to a broad range of other multidimensional relaxation and diffusion experiments.     

Tetrachloroferrate(III) Complexes Containing Some Heteroaromatic Organic Cations: Structures and Magnetic Properties

The crystal structures of tetrachloroferrate(III) complexes having stoichiometry (BH)⁺ [FeCl₄]^? (where B = isoquinoline and 4‐aminopyridine) were determined at 100 K. While weak interactions, particularly N–H···Cl hydrogen bonds, are evident in the structures, distances between the Fe(III) centers are quite long in both cases. The structure of the compound with B = quinoline was compared with that previously established at room temperature, and showed that neither solid‐solid nor magnetic phase transitions occurred in this temperature range. Magnetic measurements on the paramagnetic powders indicate weak antiferromagnetic interactions transmitted through the crystal lattice, giving rise to Néel temperatures that are significantly below 10 K. Comparisons are made with other characterized [FeCl₄]^? compounds having similar organic base cations, enabling clarification of the superexchange mechanism.     

Synthesis,characterization and radiation damage studies of high-k dielectric (HfO2) films for MOS device applications

The current trend in miniaturization of metal oxide semiconductor devices needs high-k dielectric materials as gate dielectrics. Among all the high-k dielectric materials, HfO₂ enticed the most attention, and it has already been introduced as a new gate dielectric by the semiconductor industry. High dielectric constant (HfO₂) films (10?nm) were deposited on Si substrates using the e-beam evaporation technique. These samples were characterized by various structural and electrical characterization techniques. Rutherford backscattering spectrometry, X-ray reflectivity, and energy-dispersive X-ray analysis measurements were performed to determine the thickness and stoichiometry of these films. The results obtained from various measurements are found to be consistent with each other. These samples were further characterized by I–V (leakage current) and C–V measurements after depositing suitable metal contacts. A significant decrease in the leakage current and the corresponding increase in device capacitance are observed when these samples were annealed in oxygen atmosphere. Furthermore, we have studied the influence of gamma irradiation on the electrical properties of these films as a function of the irradiation dose. The observed increase in the leakage current accompanied by changes in various other parameters, such as accumulation capacitance, inversion capacitance, flat band voltage, mid-gap voltage, etc., indicates the presence of various types of defects in irradiated samples.     

Synthesis and structural characterization of amorphous nano-sized SiBONC ceramic powders via polymer pyrolysis

SiBONC ceramic powders have been prepared via a polymer pyrolysis route using silicon tetrachloride (SiCl₄), benzaldehyde (PhCHO), boron trichloride (BCl₃) and aniline (PhNH₂) as starting materials. Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and transmission electron microscopy (TEM) were performed to investigate the structural characteristics of the polymer precursor and the ceramic powders. The SiBONC ceramic powders in spherical shape with a mean diameter of 50 nm are amorphous and composed of B-N, Si-O, Si-C, and SiON_x groups. The SiBONC ceramic powders were sintered at 1700 °C to a dense material which still remained amorphous.     

Structures, phase transitions and microwave dielectric properties of the 6H perovskites Ba3BSb2O9, B=Mg, Ca, Sr, Ba

We present a complete temperature-composition phase diagram for Ba₃BSb₂O₉, B=Mg, Ca, Sr, Ba, along with their electrical behavior as a function of B. These compounds have long been recognized as 6H-type perovskites, but (with the exception of B=Mg) their exact structures and properties were unknown due to their low symmetries, temperature-dependent phase transitions, and difficulties in synthesizing pure samples. The full range of possible space group symmetries is observed, from ideal hexagonal P6₃/mmc to monoclinic C2/c to triclinic . Direct second-order transitions between these phases are plausible according to group theory, and no evidence was seen for any further intermediate phases. The phase diagram with respect to temperature and the effective ionic radius of B is remarkably symmetrical for B=Mg, Ca, and Sr. For B=Ba, a first-order phase transition to a locally distorted phase allows a metastable hexagonal phase to persist to lower temperatures than expected before decomposing around 600 K. Electrical measurements revealed that dielectric permittivity corrected for porosity does not change significantly as a function of B and is in a good agreement with the values predicted by the Clausius-Mossotti equation.