GaAs/GaAsPBi core-shell nanowires grown by molecular beam epitaxy

We report on the growth, structural, and optical properties of GaAs/GaAsPBi core-shell nanowires (NWs) synthesized by molecular beam epitaxy (MBE). The structure presents advantageous optical properties, in particular, for near- and mid-infrared optical applications. Scanning electron microscopy shows that although the stems of GaAs/GaAsP and GaAs/GaAsBi core-shell NWs preserve the hexagonal prism shape, the GaAs/GaAsPBi core-shell NWs develop a quasi-three-fold orientational symmetry affected by the hexagonal prismatic core. Detailed structural analyses of a GaAs/GaAsPBi core-shell stem show that it crystallized with zincblende structure with a nominal shell composition of GaAs0.617P0.362Bi0.021. Photoluminescence of GaAs/GaAsPBi core-shell NWs shows the luminescent peak at 1.02 eV with high internal quantum efficiency at room temperature (IQERT ~6%) superior to those of MBE-grown GaAs core NWs and GaAsPBi multiple quantum wells earlier reported. Energy-dispersive X-ray spectroscopy performed on the GaAs/GaAsPBi core-shell NWs yields an estimated bandgap different from the optically measured value. We attribute this discrepancy to the NW compositional fluctuations that also may explain the high IQERT.

The effect of V on the morphology of TiB2 particles in as-cast aluminum composites

This study presents the modification effect of trace vanadium on the in-situ formed TiB2 particles in as-cast aluminum composites. With 0.2 wt.% V addition the morphology of TiB2 was modified from hexagonal platelet or irregular feather-like shape to hexagonal prism or rectangular prism with parallel growth steps along the c-axis. Meanwhile, V rich cores were detected in the center of TiB2 and the exposure of the high-index crystal plane (1101)TiB2 was detected in Al-0.2 wt.%V. Statistical analysis of the particle size and aspect distribution both in commercial Al and Al-0.2 wt.%V was conducted. The elemental distribution and scanning electron microscopy investigation revealed that VB2 may serve as the 2D-nucleus of TiB2 particles. The growth mechanism of TiB2 under the influence of V was explored.

Wear of 17-4 PH Stainless Steel Patterned Surfaces Fabricated Using Selective Laser Melting

The recent developments in additive manufacturing (AM) are providing unprecedented opportunities in various fields, including the fabrication of advanced materials for tribological applications. The present work describes the results of an exploratory study focused on the analysis of 17-4 PH steel surfaces obtained using selective laser melting (SLM). In particular, the study includes the analysis of baseline (as-produced) and textured steel surfaces. Surface texturing comprises hexagonal prism structures (with or without dimples) arranged in a honeycomb pattern with 50 µm or 100 µm gap spacing. Starting from the minimum printing size enabled by the 3D printing platform, various textures are prepared by scaling up the characteristic dimensions of the prisms up to 500%. The obtained surface patterns are characterized (qualitatively and quantitatively) using a non-contact computerized numerical control (CNC) measuring system. The coefficient of friction (COF) was investigated using a Ball-on-Disk configuration using bearing steel balls as counterparts. For a fixed sliding speed, different contact loads and sliding radii were considered, while the tests were carried out in either dry or lubricant-impregnated conditions. The results of wear tests in both dry and lubricated conditions indicated that the baseline samples are provided with lower COF compared to the textured ones. For the latter, neither the gap spacing nor the presence of dimples led to significant variations in the COF. However, in lubricated conditions, the values of the COF for baseline and textured surfaces were closer and much smaller. In particular, the results provide clear indications regarding reducing the gap between prisms, which had a beneficial effect on the COF in lubricated conditions. Similarly, sensitivity to dimples was quite remarkable, with a reduction in the COF of about 30% when the larger gap spacing between the prisms was used.

Predicting Bilayer B50, B52, B56, And B58: Structural Evolution In Bilayer B48–B72 Clusters

The successive experimental observations of planar, cage-like, seashell-like, and bilayer Bn–/0 clusters in the size range between n = 3–48 well demonstrate the structural diversity and rich chemistry of boron nanoclusters. Based on extensive global minimum search and density functional theory calculations, we predict herein the bilayer C1 B50 (I), C2h B52 (II), C1 B56 (IV), and C2v B58 (V) as the global minima of the systems to fill in the missing gap in the bilayer B2n series between B48–B72. These highly stable species all contain a B38 bilayer hexagonal prism at the center, with 2, 2, 3, and 3 effective interlayer B-B σ-bonds formed between inward-buckled atoms on the top and bottom layers, respectively. Our bilayer C1 B50 (I) and C1 B56 (IV) prove to be obviously more stable than the previously reported monolayer planar C2v B50 and C2v B56 with two adjacent B6 hexagonal holes. Detailed bonding analyses indicate that these bilayer clusters follow the universal bonding pattern of σ + π double delocalization, making them three-dimensionally aromatic in nature. The bilayer B2n species in the size range between B48–B72 evolve gradually on the waist around the B38 or elongated B46 bilayer hexagonal prism at the center.

Determinants of crystal structure transformation of ionic nanocrystals in cation exchange reactions

Changes in the crystal system of an ionic nanocrystal during a cation exchange reaction are unusual yet remain to be systematically investigated. In this study, chemical synthesis and computational modeling demonstrated that the height of hexagonal-prism roxbyite (Cu1.8S) nanocrystals with a distorted hexagonal close-packed sulfide anion (S2−) sublattice determines the final crystal phase of the cation-exchanged products with Co2+ [wurtzite cobalt sulfide (CoS) with hexagonal close-packed S2– and/or cobalt pentlandite (Co9S8) with cubic close-packed S2–]. Thermodynamic instability of exposed planes drives reconstruction of anion frameworks under mild reaction conditions. Other incoming cations (Mn2+, Zn2+, and Ni2+) modulate crystal structure transformation during cation exchange reactions by various means, such as volume, thermodynamic stability, and coordination environment.

Dynamic Shape Transformation of a DNA Scaffold Applied for an Enzyme Nanocarrier

Structural programmability and accurate addressability of DNA nanostructures are ideal characteristics for the platform of arranging enzymes with the nanoscale precision. In this study, a three-dimensional DNA scaffold was designed to enable a dynamic shape transition from an open plate-like structure to its closed state of a hexagonal prism structure. The two domains in the open state were folded together to transform into the closed state by hybridization of complementary short DNA closing keys at both of the facing edges in over 90% yield. The shape transformation of the DNA scaffold was extensively studied by means of the fluorescence energy transfer measurement, atomic force microscope images, and agarose gel electrophoretic analyses. A dimeric enzyme xylitol dehydrogenase was assembled on the DNA scaffold in its open state in a high-loading yield. The enzyme loaded on the scaffold was subsequently transformed to its closed state by the addition of short DNA closing keys. The enzyme encapsulated in the closed state displayed comparable activity to that in the open state, ensuring that the catalytic activity of the enzyme was well maintained in the DNA nanocarrier. The nanocarrier with efficient encapsulation ability is potentially applicable for drug delivery, biosensing, biocatalytic, and diagnostic tools.

A Proof of Concept Study of the Mechanical Behavior of Lattice Structures Used to Design a Shoulder Hemi-Prosthesis

Lattice structures offer great benefits when employed in medical implants for cell attachment and growth (osseointegration), minimization of stress shielding phenomena, and weight reduction. This study is focused on a proof of concept for developing a generic shoulder hemi-prosthesis, from a patient-specific case of a 46 years old male with a tumor on the upper part of his humerus. A personalized biomodel was designed and a lattice structure was integrated in its middle portion, to lighten weight without affecting humerus’ mechanical response. To select the most appropriate lattice structure, three different configurations were initially tested: Tetrahedral Vertex Centroid (TVC), Hexagonal Prism Vertex Centroid (HPVC), and Cubic Diamond (CD). They were fabricated in resin by digital light processing and its mechanical behavior was studied via compression testing and finite element modeling (FEM). The selected structure according to the results was the HPVC, which was integrated in a digital twin of the biomodel to validate its mechanical performance through FEM but substituting the bone material model with a biocompatible titanium alloy (Ti6Al4V) suitable for prostheses fabrication. Results of the simulation showed acceptable levels of Von Mises stresses (325 MPa max.), below the elastic limit of the titanium alloys, and a better response (52 MPa max.) in a model with equivalent elastic properties, with stress performance in the same order of magnitude than the showed in bone’s material model.