Fatigue cracking in polycrystalline NiTi was investigated using a multiscale experimental framework for average grain sizes (GS) from 10 to 1500 nm for the first time. Macroscopic fatigue crack growth rates, measured by optical digital image correlation, were connected to microscopic crack opening and closing displacements, measured by scanning electron microscope DIC (SEM-DIC) using a high-precision external SEM scan controller. Among all grain sizes, the 1500 nm GS sample exhibited the slowest crack growth rate at the macroscale, and the largest crack opening level (stress intensity at first crack opening) and minimum crack opening displacements at the microscale. Smaller GS samples (10, 18, 42, and 80 nm) exhibited nonmonotonic trends in their fatigue performance, yet the correlation was strong between macroscale and microscale behaviors for each GS. The samples that exhibited the fastest crack growth rates (42 and 80 nm GS) showed a small crack opening level and the largest crack opening displacements. The irregular trends in fatigue performance across the nanocrystalline GS samples were consistent with nonmonotonic values in the elastic modulus reported previously, both of which may be related to the presence of residual martensite only evident in the small GS samples (10 and 18 nm).

The large strain extrusion-machining process has been used to refine the microstructure in a Titanium alloy (Ti–6Al–4V). The unconstrained cutting or machining of Ti–6Al–4V entails the formation of shear localized chips at nearly all cutting speeds, thereby hindering the use of extrusion-machining to produce fine-grained materials. The present effort attempts to suppress shear localization by the suitable modification of texture in Ti–6Al–4V through the cold-rolling process prior to extrusion-machining. Ti–6Al–4V plates were cold rolled to 30, 40, 45, and 47% thickness reductions. These textured plates were extrusion machined using a suitably designed fixture leading to fine-grained continuous foils with increased hardness. Microscopy has revealed that the suppression of shear localization in the foils produced from plates which are cold rolled to more than 40% of thickness reduction is triggered by texture formation. For thickness reductions slightly lower than 40% (e.g., 30%), suppression can be achieved only by a combination of texture and extrusion.

The wettability of the 304L steel is an important parameter in Liquid Metal Embrittlement studies. Empirically, it is found to be greatly enhanced by pre-exposure to oxygenated liquid sodium. The corrosion interface formed during exposure to sodium has been analyzed at the nanoscale by transmission electron microscopy using the focused ion beam sampling. A thin layer of sodium chromite (NaxCrO2 with x ≤ 1) is detected at the interface validating wetting on an oxide mechanism for the enhanced wetting after pre-exposure. Fracture micromechanisms and the crack path of liquid sodium-embrittled austenitic steel 304L at 573 K have been investigated down to the nanoscale. High-resolution orientation mapping analyses immediately below the fracture surface show that abundant martensitic transformations (γ → α) and twinning occur during deformation of austenite. The preferential crack path is intergranular along the newly formed γ/γ interfaces. It is concluded that these transformations play a major role in the fracture process.

In this present study, different volume percentages of titanium dioxide nanoparticles were added as dispersions in commercially pure magnesium using the blend-press-sinter powder metallurgy process followed by hot extrusion. The physically blended titanium dioxide nanoparticles dispersoid induced a significant grain refinement in the extruded magnesium matrix. Characterization of the mechanical properties revealed that the increasing volume percentage of titanium oxide nanoparticles dispersion was effective in enhancing the ductility of magnesium without disturbing the strength under tensile loading and enhancing the strength of magnesium without disturbing the ductility under compressive loading. The dominating deformation mechanism in pure magnesium was the dislocation slip, which was subdued by the tensile twinning deformation mechanism due to the increasing presence of titanium dioxide dispersion. The effect of shift in the dominating deformation mechanism was displayed by the elimination of tensile-compressive asymmetry in magnesium when dispersed with 1 vol% of titanium dioxide nanoparticles.

To secure the reliability of flexible electronics, the effect of multicomponent stress on the device properties during complex mechanical deformation needs to be thoroughly understood. The electrical resistances of metal interconnects are investigated by in situ monitoring at different twisting angles and with different pattern positions. As the twisting angle increased, the electrical resistance increased earlier. Furthermore, in the line pattern located far from the central axis, severe electrical degradation and fatigue damage formation were observed. Multicomponent stress evolution during twisting was analyzed by the finite-element simulation method. For easy practical application for estimating the representative twisting strain, an analytic solution of twisting deformation was formulated and compared with the simulation. Using the equivalent strain, the fatigue lifetime was fitted, and the exponents were obtained for lifetime expectation. This systematic study provides the guidelines for highly reliable flexible devices and the tools for determining the expected fatigue lifetime.

6,13-Bis(triisopropylsilylethynyl)pentacene (TIPS-pentacene) and pentacene-based high-voltage organic thin film transistors (HVOTFTs) have been fabricated on solid and flexible substrates via a low-temperature (<100 °C) solution-processed and vacuum-deposited fabrication method. A high-k dielectric Bi1.5Zn1Nb1.5O7 and an organic dielectric parylene-C have been incorporated into the transistor design. The reliability of the HVOTFTs was analyzed under flexure, where a nonsaturating I–V characteristic behavior was observed. Here, the HVOTFT exhibited a mobility μ of 0.018 cm2/(V s) and a large breakdown voltage of |VDS| > 120 V and >550 V for TIPS-pentacene and pentacene devices, respectively. The large breakdown voltages are attributed to an organic semiconductor channel region which is partially gated, allowing for a large potential drop. Thiolphenol-based SAMs were used to help improve charge injection. Electrical measurements were also performed with samples designed with a top metal field plate to improve control of the charge carrier within the channel.

Sterilization is one of the last stages prior to the implantation of a biomaterial. Therefore, the method should be chosen carefully as this is determinant not to compromise the properties of the material. In this context, three sterilization processes were evaluated as to their effect on the properties of a silane hybrid coating: steam autoclave, ethylene oxide, and hydrogen peroxide plasma. The coating was obtained from a sol consisting of alkoxysilane Tetraethoxysilane and organoalcoxysilane Methyltriethoxysilane (MTES), applied to the Ti6Al4V substrate, to increase its corrosion resistance and biocompatibility. After sterilization, the samples were characterized by scanning electron microscopy, atomic force microscopy, profilometry, wetabillity, and Fourier transform infrared spectroscopy. The electrochemical behavior was monitored by open circuit potential and potentiodynamic polarization curves. The cytocompatibility was evaluated by adhesion, viability, and morphological alterations in the MG-63 cells. The results showed that the protective behavior of the hybrid coating was compromised regardless of the sterilization method. However, the steam autoclave caused more morphological changes on the silane hybrid coating as well as on the Ti6Al4V substrate than the other two sterilization methods. Although the sterilized hybrid coating did not show cytotoxicity, the hybrid coating sterilized by hydrogen peroxide plasma showed a higher percentage of viable cells. The ethylene oxide presented the lowest percentage of viability and the highest cell death rate.

Chronic osteomyelitis, a bone infection caused by bacteria, requires extensive parenteral treatments. With an aim to develop bioactive glass with antibacterial properties to resist such infections, bioactive glasses with bismuth oxide as the dopant in various amounts up to 8 wt% were prepared. X-ray diffraction patterns and Fourier-transform infrared spectra of glass samples after immersion in simulated body fluid showed the presence of hydroxyapatite (HAp) and hydroxyl carbonate apatite for all samples except with the one having Bi2O3 substitution of 8 wt%. In vitro cell proliferation by MTT assay studies using a mouse fibroblast cell line (NIH3T3) have also been carried out. Primary antimicrobial activity of the glass particles was analyzed against Escherichia coli (E. coli) using broth microdilution method which exhibited bacteriostatic effects and bactericidal properties in selected samples. The combination of bioactivity, cell proliferation, and antibacterial properties of selected Bismuth-containing bioactive glasses could be exploited in treating bone-related infections.

Luminescent biolabels are being eagerly investigated as a means of detecting cancer cells by bioimaging. Upconversion nanoparticles are a promising option to be used as biolabels for cancer cell detection. This process uses a near infrared beam (NIR λ = 980 nm) as the excitation source to upconvert the energy into light in the visible region. The present study, used Y2O3:Yb3+, Er3+ (1%, 10% mol) and Gd2O3:Yb3+, Er3+ (1%, 10% mol) capable of emitting red photons of λ = 660 nm. The nanoparticles were previously functionalized with aminosilanes and folic acid (UCNP-NH2-FA). Folic acid binds to the folate receptor on the surface of MCF-7 breast cancer cells, and this binding promotes internalization of the UCNPs via endocytosis. The UCNPs were characterized by TEM, EDS, and Fourier transform infrared. Cytotoxicity was also analyzed using the MTT (methy-134 thiazolyltetrazolium) colorimetric assay. The UCNPs-NH2-FA was noncytotoxic to the studied cancer cells and they were clearly localizable within the cell cytoplasm via confocal microscope.

The novel visible-light-responsive direct solid-state Z-scheme g-C3N4/BiOI heterojunction has been synthesized successfully by means of a solid phase calcination method and used for the degradation of microcystin-LR (MC-LR). The layered g-C3N4 disperses on the surface of BiOI microspheres. The samples are characterized by FESEM, HRTEM, XRD, FT-IR, UV-vis spectroscopy, XPS, BET, PL, and Mott–Sckottky. The photocatalytic activity and photodegradation mechanism of the as-prepared g-C3N4/BiOI microsphere photocatalysts are conducted under visible light irradiation using MC-LR as the target pollutant. The g-C3N4/BiOI material exhibits superior photocatalytic performance when compared with pure BiOI, the possible reason is the efficient separation of photogenerated carriers at the interface between g-C3N4 and BiOI. The heterostructure is responsible for the improved separation efficiency of photogenerated electron–hole pairs and thus the higher photocatalytic activity. The possible photocatalytic mechanism is proposed based on relative band positions of these two semiconductors.

Designing advanced nonprecious metal electrocatalysts to reduce overpotential and accelerate hydrogen evolution reaction (HER) has attracted considerable attention. However, improving the sluggish kinetics for electrocatalytic HER in alkaline media is still a great challenge. Herein, we found that amorphous NiO nanoclusters directly grown on nickel foam (NiO/NF) as a bifunctional HER catalyst demonstrated an ultrahigh electrocatalytic activity in alkaline environment. Such excellent HER performance of NiO/NF might mainly originate from the exposed interfaces of metallic Ni and amorphous NiO. The coordinatively unsaturated amorphous NiO domain is propitious to the adsorption of water molecule and the successive cleavage of HO–H bond, while the neighboring metallic Ni domain is beneficial to the adsorption of resulting Hads intermediate and recombination into hydrogen molecules, thus expediting the HER toward lower overpotential. These findings may open a window to the design and preparation of earth-abundant, low-cost metal oxide/metal electrocatalysts with desirable HER activities.

U–Mo metallic alloy is considered as an advanced fast reactor and research reactor fuel material. U–33 at.% Mo has a higher melting point than that of pure uranium metal. This provides a higher safety margin against fuel melting and diminishes fuel and clad interaction. The metallic fuels are fabricated through a melting-casting route, and the cast microstructure of U–33 at.% Mo has been characterized using optical microscope, scanning electron microscopy—energy dispersive spectroscopy, and Electron back scattered diffraction. These microstructures show dendrites of two different morphologies: (i) the γ-(U) dendrite with secondary branches and (ii) the equiaxed (Mo) dendrite without secondary branches and surrounded by a peritectic reaction product. In this article, for the first time, a phase field model has been developed for U–Mo alloys to understand the morphological evolution and the associated microsegregation of γ-(U) dendrites in the U–33 at.% Mo alloy. The evolution of the concentration and temperature field with the time and the effect of undercooling on the growth velocity of γ-(U) and (Mo) dendrites has been studied.