Search Results (166)

In this paper, we perform crystal plasticity finite element (CPFE) simulations of spherical nanoindentation to extract the indentation stress–strain (ISS) curve for a single-crystalline copper. The load–displacement curves on the Cu (010) surface at incremental indentation depths are obtained. Surface pile-up topography is explored and characterized by the activated slip systems on the indented surface and stress distribution on the cross-section to reveal the crystal anisotropy. And the effect of indentation depth on the stiffness and surface pile-up height is further analyzed. Finally, the zero point is defined, and the indentation stress–strain (ISS) curve is extracted from load–displacement curves. The validity of the ISS curve is demonstrated for crystalline copper materials by comparing measured results published in the literature. Full article

This paper reports on the anisotropic optoelectronic properties of aligned poly(3-hexylthiophene) (P3HT) nanowire (NW) arrays fabricated via blade coating and UV irradiation, exhibiting a remarkably high electrical resistance anisotropy ratio of up to 8.05 between the parallel (0°) and perpendicular (90°) directions. This resistance anisotropy originates from the advantage of directional charge transport. Optimized $5 \mathrm{m}\mathrm{g}/\mathrm{m}\mathrm{L}$ P3HT solutions under 32 min UV irradiation yielded unidirectional π-π*-stacked NWs with enhanced crystallinity. Polarized microscopy and atomic force microscopy confirmed high alignment and dense NW networks. The angular dependence of polarization exhibits a cosine-modulated response, while the angular anisotropy of the measured photocurrent points to structural alignment rather than trap-state control. The scalable fabrication and tunable anisotropy demonstrate potential for polarization-sensitive organic electronics and anisotropic logic devices. Full article

This study focused on investigations of FeCo and FeNi nanowires prepared by template-assisted electrodeposition in polycarbonate membranes. Nanowires with a diameter of 100 nm and length of 6 µm were grown at different cathodic potentials and electrolyte compositions. Scanning electron microscopy images revealed densely packed arrays of continuous nanowires with smooth surfaces without visible porosity, regardless of the applied potential. Chemical analysis of nanowires pointed out weak sensitivity of chemical composition on the electrodeposition potential in the case of FeCo nanowires, in contrast to FeNi nanowires, where the increase of the cathodic potential resulted in higher Ni content. X-ray diffraction studies showed polycrystalline structure for all samples indicating B2 phase (Pm-3m) with isotropic growth of FeCo nanowires and FeNi₃ phase with a preferential growth along [111] direction in the case of FeNi nanowires. The peak broadening suggests a fine crystalline structure for both FeCo and FeNi materials with average crystallite sizes below 20 nm. Magnetic studies indicated an easy axis of magnetization parallel to the nanowire axis for all FeCo nanowires and potential-dependent anisotropy for FeNi nanowires. The present studies thus suggested the feasibility of producing segmented nanowires based on FeNi alloys, while poor chemical sensitivity to the applied potential was observed for the FeCo system. Full article

By performing first-principles calculations, we predicted a kind of novel ultrathin two-dimensional (2D) ferromagnet, single-atomic-layer EuN. EuN monolayer is a ferromagnetic half-metal with a large band gap of 1.69 eV; Eu ions in EuN are in the highest spin state and have large magnetic moments of 6 μB, much larger compared with the non-rare-earth (RE) metal ions. The magneto-crystalline anisotropy energy (MCE) of EuN monolayer is −3.72 meV per Eu ion, which is much higher than that of CrI₃ monolayer (0.685 meV per Cr ion); the magnetic dipolar energy (MDE) enhances magnetic anisotropy for EuN monolayer; large magnetic anisotropy energy (MAE) is beneficial to stabilizing the long-range ferromagnetic ordering. More importantly, different from many RE metal monolayers, hybridization between Eu-f and N-p orbitals induces ferromagnetism for EuN monolayer; the Curie temperature of EuN monolayer is above the liquid-nitrogen temperature (100 K). Additionally, the Curie temperature of EuN monolayer increases with increasing biaxial strain due to increased f-p hybridization. Full article

Fluorinated ethylene propylene (FEP) films were subjected to heat, UV, and heat–UV treatments. Structural changes that occurred after these treatments were recorded via X-ray diffraction (XRD), microtensile, and laser ablation testing. XRD macromolecular orientation texture analysis revealed changes in the fraction of crystalline components and the degree of anisotropy of the FEP films after being subjected to different processing conditions. Heat treatment at 200 °C affected structural properties by rearranging the crystallites and resulting in a higher degree of anisotropy. By contrast, the UV treatment of FEP resulted in a lower degree of anisotropy. The changes in anisotropy and crystallinity of FEP films significantly affected their Young’s modulus and yield stress. The UV laser ablation threshold values were found to be lower for the heat-treated FEP films. Full article

Thermoplastic composite pipes (TCP) consist of three distinct layers—liner, reinforcement, and coating—offering superior advantages over traditional industrial pipes, including flexibility, lightweight construction, and corrosion resistance. This study systematically characterises the thermal properties of TCP layers and their compositions using a multi-method approach. Thermal analysis was conducted through differential scanning calorimetry (DSC) for isothermal and non-isothermal crystallisation, thermogravimetric analysis (TGA) for thermal stability, and Fourier transform infrared spectroscopy (FTIR) for material identification. FTIR confirmed polyethylene as the primary component of TCP, with compositional variations across the layers. TGA results indicated that thermal degradation begins at approximately 200 °C, with complete decomposition at 500 °C. DSC analysis revealed a double melting peak, prompting further investigation into its mechanisms. On-isothermal crystallisation kinetics, analysed at cooling rates of 10 °C/min and 50 °C/min, revealed an anisotropic crystalline growth pattern. Although nucleation occurs uniformly, the subsequent three-dimensional crystalline growth is governed more by the degree of supercooling than by the crystallography of the glass fibres. This underscores the importance of precisely controlling the cooling rate during manufacturing to optimise the anisotropic properties of the reinforced layer. This study also demonstrates the value of FTIR, TGA, and DSC techniques in characterising the thermo-physical behaviour of TCP, offering critical insights into thermal expansion, shrinkage phenomena, and overall material stability. Given the limited body of research on this specific TCP formulation, the findings presented here lay a foundation for both quality enhancement and process optimisation. Moreover, the paper offers a distinctive perspective on the dynamic behaviour, thermal expansion, and long-term performance of TCP in demanding oil and gas environments. Full article

Due to their high refractive index, record optical anisotropy and a set of excitonic transitions in visible range at a room temperature, transition metal dichalcogenides have gained much attention. Here, we adapted a femtosecond laser ablation for the synthesis of WSe₂ nanoparticles (NPs) with diameters from 5 to 150 nm, which conserve the crystalline structure of the original bulk crystal. This method was chosen due to its inherently substrate-additive-free nature and a high output level. The obtained nanoparticles absorb light stronger than the bulk crystal thanks to the local field enhancement, and they have a much higher photothermal conversion than conventional Si nanospheres. The highly mobile colloidal state of produced NPs makes them flexible for further application-dependent manipulations, which we demonstrated by creating substrates for SERS sensors. Full article

To investigate the influence of aggregate crystalline surface anisotropy on the interfacial effects and understand the bonding mechanisms, molecular dynamics simulations were employed to analyze the spatial distribution, diffusion, and adhesion properties of asphalt on typical acidic (α-quartz, SiO₂) and weakly alkaline (calcite, CaCO₃) aggregates. The results indicated that different types and crystalline surfaces of aggregates did not alter the distribution patterns of the asphalt components on their surfaces. However, the magnitude of the radial distribution function (RDF) varied with different crystalline surfaces, and a higher RDF value was correlated with better adhesion performance. Different diffusion behaviors were exhibited by asphalt molecules on different crystalline surfaces: slower diffusion was correlated with stronger adhesion and faster diffusion with weaker adhesion. The adhesion performance was significantly affected by the anisotropy of the aggregates. In the asphalt–SiO₂ system, the van der Waals energy and surface atomic density were the major influencing factors, whereas, in the asphalt–CaCO₃ system, the electrostatic energy was significantly influenced by ionic bonding. Overall, alkaline aggregates showed greater adhesion performance with asphalt than acidic aggregates. Full article

Monolayer nanosheets of zirconium phosphate in aqueous suspension exhibit short-range repulsion and long-range attraction, producing, at overall volume fractions larger than about half a percent, phase separation into higher-concentration liquid crystal and lower-concentration isotropic regions. At high concentrations, this phase separation takes the form of an emulsion of condensed, liquid-crystalline droplets, which anneal to form lens-shaped tactoids. These tactoids provide an opportunity to study the liquid crystal ordering of inorganic nanosheets in the limit of large shape anisotropy (diameter/thickness~400) and high packing fraction (volume fraction $\gtrsim$ 70%). The internal liquid crystal structure of the tactoids remains nematic even under conditions that would usually favor ordering into lamellar smectics. Local lamellar ordering is suggested by short-range, smectic-like layer correlations, but a full transition into a smectic phase appears to be inhibited by the nanosheet edges, which act as a perturbative population of dislocation loops in the system of layers. Under conditions of thermal equilibrium, the nanoplates organize positionally to enable bend deformation of the director, a hallmark of the nematic phase and its principal distinction from the smectic, where bend must be expelled. Full article

Crystalline active pharmaceutical ingredients with comparable size and surface area can demonstrate surface anisotropy induced during crystallization or downstream unit operations such as milling. To the extent that varying surface properties impacts bulk powder properties, the final drug product performance such as stability, dissolution rates, flowability, and dispersibility can be predicted by understanding surface properties such as surface chemistry, energetics, and wettability. Here, we investigate the surface properties of different batches of Odanacatib prepared through either jet milling or fast precipitation from various solvent systems, all of which meet the particle size specification established to ensure equivalent biopharmaceutical performance. This work highlights the use of orthogonal surface techniques such as Inverse Gas Chromatography (IGC), Brunauer–Emmett–Teller (BET) surface area, contact angle, and X-ray Photoelectron Spectroscopy (XPS) to demonstrate the effect of processing history on particle surface properties to explain differences in bulk powder properties. Full article

We present theoretical investigations examining the electronic and magnetic properties of the SmFe_12−xMo_x (x = 1, 2) and SmFe₁₀Mo₂H compounds, including magneto-crystalline anisotropy, magnetic moments, exchange-coupling parameters, and Curie temperatures. The spin-polarized fully relativistic Korringa–Kohn–Rostoker (SPR-KKR) band structure method has been employed, using the coherent potential approximation (CPA) to deal with substitutional disorder. Hubbard-U correction was applied to the local spin density approximation (LSDA+U) in order to account for the significant correlation effects arising from the 4f electronic states of Sm. According to our calculations, the total magnetic moments increases with H addition, in agreement with experimental data. Adding one H atom in the near-neighbor environment of the Fe 8j site reduces the magnetic moments of Fe 8j and enhances the magnetic moment of Fe 8f. For every investigated alloy, the site-resolved spin magnetic moments of Fe on the 8i, 8j, and 8f sites exhibit the same magnitude sequence, with $m_s^{Fe}$ (8i) > $m_s^{Fe}$ (8j) > $m_s^{Fe}$ (8f). While the addition of H has a positive impact on magneto-crystalline anisotropy energy (MAE), the increase in Mo concentration is detrimental to MAE. The computed exchange-coupling parameters reveal the highest values between the closest Fe 8i spins, followed by Fe 8i and Fe 8j spins, for all investigated alloys. The Curie temperature of the alloys under investigation is increased by decreasing the Mo concentration or by H addition, which is qualitatively consistent with experimental findings. Full article

Iron–chalcogenide superconductors continue to captivate researchers due to their diverse crystalline structures and intriguing superconducting properties, positioning them as both a valuable platform for theoretical investigations and promising candidates for practical applications. This review begins with a comprehensive overview of the fabrication techniques employed for various iron–chalcogenide superconductors, accompanied by a summary of their phase diagrams. Subsequently, it delves into the upper critical field, anisotropy, and critical current density. Furthermore, it discusses the successful fabrication of meters-long coated conductors and explores their applications in superconducting radio-frequency cavities and coils. Finally, several prospective avenues for future research are proposed. Full article

GaN on Si plays an important role in the integration and promotion of GaN-based wide-gap materials with Si-based integrated circuits (IC) technology. A series of GaN film materials were grown on Si (111) substrate using a unique plasma assistant molecular beam epitaxy (PA-MBE) technology and investigated using multiple characterization techniques of Nomarski microscopy (NM), high-resolution X-ray diffraction (HR-XRD), variable angular spectroscopic ellipsometry (VASE), Raman scattering, photoluminescence (PL), and synchrotron radiation (SR) near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. NM confirmed crack-free wurtzite (w-) GaN thin films in a large range of 180–1500 nm. XRD identified the w- single crystalline structure for these GaN films with the orientation along the c-axis in the normal growth direction. An optimized 700 °C growth temperature, plus other corresponding parameters, was obtained for the PA-MBE growth of GaN on Si, exhibiting strong PL emission, narrow/strong Raman phonon modes, XRD w-GaN peaks, and high crystalline perfection. VASE studies identified this set of MBE-grown GaN/Si as having very low Urbach energy of about 18 meV. UV (325 nm)-excited Raman spectra of GaN/Si samples exhibited the GaN E₂(low) and E₂(high) phonon modes clearly without Raman features from the Si substrate, overcoming the difficulties from visible (532 nm) Raman measurements with strong Si Raman features overwhelming the GaN signals. The combined UV excitation Raman–PL spectra revealed multiple LO phonons spread over the GaN fundamental band edge emission PL band due to the outgoing resonance effect. Calculation of the UV Raman spectra determined the carrier concentrations with excellent values. Angular-dependent NEXAFS on Ga K-edge revealed the significant anisotropy of the conduction band of w-GaN and identified the NEXAFS resonances corresponding to different final states in the hexagonal GaN films on Si. Comparative GaN material properties are investigated in depth. Full article

Our objective is to achieve a new good-quality and mechanically durable high-transparency material that, when activated by rare earth ions, can be used as laser sources, scintillators, or phosphors. The best functional transparent ceramics are formed from high-symmetry systems, mainly cubic. Considering hexagonal hydroxyapatite, which shows anisotropy, the particle size of the initial powder is extremely important and should be of the order of several tens of nanometers. In this work, transparent micro-crystalline ceramics of non-cubic Ca₁₀(PO₄)₆(OH)₂ calcium phosphate were fabricated via Spark Plasma Sintering (SPS) from two types of nanopowders i.e., commercially available (COM. HA) and laboratory-made (LAB. HA) via the hydrothermal (HT) protocol. Our study centered on examining how the quality of sintered bodies is affected by the following parameters: the addition of LiF sintering agent, the temperature during the SPS process, and the quality of the starting nanopowders. The phase purity, microstructure, and optical transmittance of the ceramics were investigated to determine suitable sintering conditions. The best optical ceramics were obtained from LAB. HA nanopowder with the addition of 0.25 wt.% of LiF sintered at 1000 °C and 1050 °C. Full article

This study investigates polyethylene glycol (PEG) homopolymer thin film adsorption on gold surfaces of controlled surface chemistry. The conformational states of physisorbed PEG are analyzed through polarization modulation infrared reflection–absorption spectrometry (PM-IRRAS). The PM-IRRAS principle is based on specific optical selection rules allowing the detection of surface-specific FTIR response of thin polymer films on the basis of differential reflectivity at the polymer/substrate interface for p- and s-polarized light. The intensification of the electric field generated at the PEG/substrate interface for p-polarized IR light in comparison with s-polarized light permits the analysis of PEG chain anisotropy and conformational changes induced by the adsorption. Results showed that PEG adsorbs on model substrates having a rather hydrophilic character in a way that the PEG chains spread parallel to the surface. In the case of a very hydrophilic substrate, the adsorbed PEG chains are in a stable thermodynamic state which allows them to arrange and crystallize as stacked crystalline lamellae after adsorption. The surface topography and morphology of the PEG thin films were also investigated by atomic force microscopy (AFM). While in the bulk state, PEG crystallizes in the form of large spherulites; on substrates whose adsorption is favored by surface chemistry, PEG crystallizes in the form of stacked lamellae with a thickness equal to 20 nm. Conversely, on a hydrophobic substrate, the PEG chains do not crystallize and adsorption occurs in the statistical coil state. Full article