Anomalous eutectics in the solidification structure of undercooled Ni–18.7 at.% Sn eutectic alloy were examined by optical metallography and electron backscattered diffraction. It was revealed that α–Ni particulates are, in principle, randomly distributed in the anomalous eutectics in the undercooling range investigated. Another eutectic phase, β–Ni3Sn, is well orientated at low undercoolings but gradually becomes inconsistent in orientation as undercooling increases, accompanied by an increasing number of grain boundaries in it. As the solidification structure changes from a mixture of anomalous eutectics plus lamellar eutectics to full anomalous eutectics beyond a critical undercooling of 130 K, however, misorientation in the β–Ni3Sn phase disappears completely from the measurement area. Partial remelting of the primary solid was proposed to be the origin of the anomalous eutectic formation, and quantitative analyses were performed.

Three-point bend test coupled with transmission electron microscopy (TEM) analysis was carried out on individual tungsten oxide nanowires (NWs) before and after annealing. Three-point bend test monitors the change in the Young’s modulus of the NW after annealing, while TEM provides nanostructural detail changes on the same NW. In this way, insight into the correlation between the mechanical properties of a NW and its nanostructure details can be obtained. Annealing increased the diameter of the NWs by forming a uniform amorphous/polycrystalline outer coating. The coating results in a decrease in Young’s moduli for thicker NWs. On the other hand, annealing led to increased Young’s moduli of thinner NWs, which is attributed to the improved crystallinity in these NWs after annealing. This study points to a more refined strategy for more in-depth understanding of the relationship between the nanostructures and elastic mechanical properties of NWs.

In this contribution, we briefly discuss how various physicochemical properties of surfaces affect the wettability and self-cleaning character of both naturally occurring and synthetic surfaces. Using a few selected examples from nature, we discuss the superhydrophobic effect and antifouling character of such surfaces and how these properties are associated with variations in surface chemical composition and topography. We also review a few special case studies aimed at adopting these biomimetic schemes to design and fabricate functional self-cleaning surfaces.

In a compression test for a Zr-based bulk metallic glass, a dominant shear band was preserved before fracture by a cylindrical stopper. A heat-affected zone (HAZ) ∼10 μm thick together with shear band was discovered in the center of the deformed sample by preferential ion milling. By using a low aspect ratio sample for compression, diverse micron-scaled HAZs among multiple shear bands were also revealed. Based on above experimental results and the isothermal source model, it was found that the thickness of shear band and its HAZ increased continuously with the progression of shear deformation.

The microstructures, interfacial reactions, and bonding strength properties of the Ti–Cu dissimilar joints using a commercially available Ag–28Cu–2Ti filler were studied, particularly as they relate to the role of an Ag barrier layer at the Ti interface. A joint microstructure and interfacial reactions closely related to the formation of brittle interfacial Ti–Cu intermetallics were fully dominated by the presence of the Ag layer at the Ti interface. Reliable Ti(base)/TiAg/Ag/Ag–Cu eutectic/Cu(base) joints without any detrimental Ti–Cu intermetallics were achieved at low brazing temperatures below 810 °C by applying an Ag interlayer of suitable thickness. It was notable that their bonding strengths were strong enough to exceed the strength of a Cu bulk base metal. This research demonstrates the potential application of an Ag interlayer for the reliable Ti–Cu dissimilar joints.

The temperature dependence of the thermal stability in a NiCoCrAlY coating alloy was examined by experimental observation and thermodynamic modeling in the 400–1200 °C temperature range. The results indicated that the thermal stabilities of primary β–NiAl, β–NiAl/α–Cr eutectic, and γ–Ni were slightly temperature dependent, but those of γ′–Ni3Al, σ–(Cr,Co,Ni), and α–Cr were strongly temperature dependent in the annealed NiCoCrAlY specimens. The temperature dependence of the thermal stabilities among γ′–Ni3Al, σ–(Cr,Co,Ni), and α–Cr might be ascribed to the σ → α transformation at ∼1100 °C and the γ′ → γ transformation at ∼800 °C. Further, using Thermocalc associated with TTNi7 database, thermodynamic equilibria were calculated. The modeling results were compared with the experimental results and found to be in reasonable agreement with the experimental observations of β–NiAl, σ–(Cr,Co,Ni), and γ′–Ni3Al. Some deviations observed are discussed in the light of both limited availability of thermodynamic data and experimental problems.

In the present work, the oxide layers developed at elevated temperature on three vanadium-free titanium alloys, of interest as implant biomaterials, were studied by Rutherford backscattering spectroscopy, elastic recoil detection analysis, and scanning electron microscopy. The chemical composition of the alloys investigated, in wt%, was Ti–7Nb–6Al, Ti–13Nb–13Zr, and Ti–15Zr–4Nb. Upon oxidation in air at 750 °C, an oxide scale forms, with a chemical composition, morphology, and thickness that depend on the alloy composition and the oxidation time. After equal exposure time, the Ti–7Nb–6Al alloy exhibited the thinnest oxide layer due to the formation of an Al2O3-rich layer. The oxide scale of the two TiNbZr alloys is mainly composed of Ti oxides, with small amounts of Nb and Zr dissolved. For both TiNbZr alloys, the role of the Nb-content on the mechanism of the oxide formation is discussed.

Hybrid thick films were deposited on Surlyn, a copolymer of poly(ethylene- co-methacrylic acid) and a common adhesion film for metal surfaces. Hybrid organic–inorganic materials were prepared by a sol-gel process. Methyltriethoxysilane (MTES) with tetraethoxysilane (TEOS), phenyltriethoxysilane (PhTES) with TEOS, and methyltrimethoxysilane (MTMS) with tetramethoxysilane (TMOS) were investigated. The inorganic component was selected to form the network for the film, while the organic component was selected to repel water and fill porosity. The films were deposited on Surlyn and on glass slides. The properties of the films were investigated using attenuated total reflection Fourier transform infrared (FTIR) and Raman spectroscopy. Contact-angle measurements indicated that the contact angle increased from ∼76.5° for Surlyn alone to ∼89.6° for Surlyn coated with MTES.

Self-healing is receiving an increasing amount of interest worldwide as a method to address damage in materials. In particular, for advanced high-performance fiber-reinforced polymer (FRP) composite materials, self-healing offers an alternative to employing conservative damage-tolerant designs and a mechanism for ameliorating inaccessible and invidious internal damage within a structure. This article considers in some detail the various self-healing technologies currently being developed for FRP composite materials. Key constraints for incorporating such a function in FRPs are that it not be detrimental to inherent mechanical properties and that it not impose a severe weight penalty.

Upconversion luminescence (UPL) characteristics and effects of Li+ ion on the UPL of ZnWO4:Yb,Er polycrystalline phosphors were investigated. It was shown that introduction of Li+ ions could reduce the calcination temperature by about 200 °C and increase the crystallinity of ZnWO4:Yb,Er by a liquid-phase sintering process via formation of Li2WO4 and other intermediates. UPL efficiency is remarkably promoted by Li+ ions. Moreover, the UPL spectrum of Li+-doped ZnWO4:Yb,Er presents a red shift, and the strongest peak position shifts from 553 to 559 nm. These can be attributed to a shift in the 4f level barycenter to lower energy, which results from lowering of the symmetry of the crystal field around Er3+.

Over the past ten years, a broad range of self-healing materials, systems that can detect when they have been damaged and heal themselves either spontaneously or with the aid of a stimulus, has emerged. Although many unique compositions and components are used to create these materials, they all employ basic chemical reactions to facilitate repair processes. Kinetically controlled ring-opening reactions and reversible metal–ligand interactions have proven useful in autonomic self-healing materials, which require no stimulus (other than the formation of damage) for operation. In contrast, nonautonomic self-healing materials, which require some type of externally applied stimulus (such as heat or light) to enable healing functions, have capitalized on chemistries that utilize either reversible covalent bonds or various types of noncovalent interactions. This review describes the underlying chemistries used in state-of-the-art self-healing materials, as well as those currently in development.

In this work, we study the cooling behavior of several typical bulk glassy alloys on casing and present the relationship between the thermal conductivity of a glassy alloy and the cooling rate upon mold casting. The cooling rates obtained for Ti-, Zr-, Pd-, and Cu-based bulk glass forming alloys are found to scale with the thermal conductivities of the studied glassy alloys.

Biological systems have the ability to sense, react, regulate, grow, regenerate, and heal. Recent advances in materials chemistry and micro- and nanoscale fabrication techniques have enabled biologically inspired materials systems that mimic many of these remarkable functions. This issue of MRS Bulletin highlights two promising classes of bioinspired materials systems: surfaces that can self-clean and polymers that can self-heal. Self-cleaning surfaces are based on the superhydrophobic effect, which causes water droplets to roll off with ease, carrying away dirt and debris. Design of these surfaces is inspired by the hydrophobic micro- and nanostructures of a lotus leaf. Self-healing materials are motivated by biological systems in which damage triggers a site-specific, autonomic healing response. Self-healing has been achieved using several different approaches for storing and triggering healing functionality in the polymer. In this issue, we examine the most successful strategies for self-cleaning and self-healing materials and discuss future research directions and opportunities for commercial applications.

The amorphous-to-crystalline transformation behavior of Fe48Cr15Mo14Y2C15B6 bulk metallic glasses was first investigated by high-temperature differential scanning calorimetry. Three events were detected with onset temperatures at 922, 975, and 1036 K, respectively. In situ synchrotron radiation x-ray diffraction patterns were collected during continuous heating and analyzed with the Rietveld approach. To describe simultaneously the amorphous fraction and crystallization products as a function of temperature, a paracrystalline structure-factor model was developed. It was included for quantitative evaluation of the amorphous phase, together with the structure factor of Cr23C6- and Fe3Mo3C-type phases observed during crystallization. Volume fractions of phases as well as lattice parameters, average lattice disorder, and crystallite size of the crystallized phases have been followed as a function of temperature. In this way, the structure evolution and thermal events have been closely inspected and accounted for by a crystallization mechanism.