A comprehensive understanding of the growth pattern of intermetallic compounds (IMCs) during solidification is critical to both the crystal-growth theory and its property optimization. In this article, growth pattern and three-dimensional (3D) morphology of primary Al6Mn IMC were investigated in directionally solidified Al–3 at.% Mn alloy at a wide range of growth rates. A transition from faceted (<60 μm/s) to nonfaceted growth (>100 μm/s) was observed with increasing growth rates. Correspondingly, 3D morphologies of primary Al6Mn change from a solid polyhedron to a hollow structure, and then to a dendrite. This kind of change is associated with the competitive growths of different crystal planes determined by the crystallographic anisotropy and growth kinetics of Al6Mn. A growth model based on atomic cluster attachment is proposed to reveal the growth transition, and a growth-rate ratio between different crystal planes is used to appropriately reveal the formation mechanism of different morphologies at low rates.

MTiO3 (M = Ca, Ni, and Zn) nanocrystals were prepared via a facile ethylene glycol-mediated synthesis route followed by calcination in air. The structures and morphologies of nanocrystals were characterized by x-ray diffraction, Raman spectroscopy, transmission electron microscopy, and scanning electron microscopy. The results indicated that CaTiO3 and NiTiO3 are orthorhombic phase, while the ZnTiO3 is orthorhombic phase. The activity of the CaTiO3 nanocrystals for water splitting into H2 was obviously higher than those of the NiTiO3 and ZnTiO3 nanocrystals, which could be attributed to the more negative conduction band position of CaTiO3 than NiTiO3 and ZnTiO3. The Brunauer–Emmett–Teller system-based surface areas of samples are 19.03, 21.13, and 4.17 m2/g for CaTiO3, NiTiO3, and ZnTiO3 nanocrystals, respectively. In addition, the activity of the CaTiO3 nanocrystals increased with increase in the sintering temperature of samples.

Thermally stable nanosized Al2O3 particles and carbon nanotubes (CNTs) are comparatively effective in simultaneous improvement of strength and ductility of wrought magnesium alloy AZ31 when incorporated in microstructure. Understanding the comparative effectiveness of these nanosized reinforcements on the high temperature deformation process of wrought AZ31 alloy is important for its potential wider automotive body application. The current study has revealed that both reinforcements are competitively effective in inducing matrix grain and intermetallic particles refinement and strengthening almost to a theoretically predicted value. Although high temperature flow stress of AZ31 was found to closely match due to incorporation of both of the nanosized reinforcements, alumina was more efficient in improving the failure strain of matrix alloy. Addition of remarkably a small amount of nanosized alumina particles or CNTs introduced huge potential in near net shape formability of AZ31 alloy at a temperature much below than the widely used 350 °C. Among the two reinforcements used in this study, alumina was found to be more efficient when compared to the effect of CNTs.

New methods for the synthesis and deterministic assembly of advanced classes of nanomaterials enable integration of high-performence semiconductors with elastomeric substrates. These capabilities provide the foundations for a high-performance electronic and optoelectronic technology that can offer linear elastic mechanical responses to large strain deformations. The results create new opportunities in materials and device engineering, with important consequences in fields ranging from biomedicine to machine vision. This article summarizes the key materials science concepts and presents illustrative examples of their recent use in injectable, cellular-scale optoelectronic devices and in hemispherical compound eye cameras.

Diamond, because of its unique physical, chemical, and electrical properties and the feasibility of growing it in thin-film form, is an ideal choice as a material for the fabrication of reliable, long endurance, microelectromechanical/nanoelectromechanical systems (MEMS/NEMS). However, various practical challenges, including wafer-scale thickness uniformity, CMOS compatibility, surface micromachining, and, more importantly, controlling the internal stress of the diamond films, make this material more challenging for MEMS engineers. Recent advances in the growth of diamond films using chemical vapor deposition have changed this landscape since most technical hurdles have been overcome, enabling a new era of diamond-based MEMS and NEMS development. This article discusses a few examples of MEMS and NEMS devices that have been fabricated using mono-, nano-, and ultrananocrystalline diamond films as well as their performance.

Diamond offers a unique combination of extreme physical properties. For many technological applications, diamond samples of the highest crystal quality are required to utilize the ultimate potential of the material. Specifically, grain boundaries, as in polycrystalline films, have to be avoided. In this article, the two major current approaches of synthesizing single crystal diamond by chemical vapor deposition are described. In homoepitaxy, high gas pressure and high power density microwave discharges facilitating growth rates above 50 µm/h form the basis for the deposition of mm-thick single crystal samples. Cloning and tiling followed by homoepitaxial overgrowth are promising novel concepts aimed at an increase in the lateral dimensions. Heteroepitaxial deposition on large-area single crystals of a foreign material represents a second alternative approach. The state of the art for both concepts is summarized, and current as well as potential future applications are discussed.

Titanium oxide (TiO2) nanoparticles (NPs) were doped with vanadium using a novel, facile, and inexpensive method. The TiO2 NPs were dispersed in a vanadyl oxalate solution prepared by dissolving vanadium pentoxide (V2O5) in oxalic acid. A short heat treatment at 400 °C applied to the dried mixture resulted in the doping of TiO2 with a net measured decrease of its band gap by about 0.5 eV, making this important semiconductor material usable in the visible light spectrum.

Recent advances in biotechnology have fueled a need for well-defined, highly stable interfaces modified with a variety of biomolecules. Diamond is a particularly attractive material for biological applications because of its chemical stability and good biocompatibility. Since diamond can be made conductive by doping, it is also of interest for a variety of electrically based biological sensing applications that achieve improved performance through selective biological modification. Recent developments of diamond growth by chemical vapor deposition have enabled the preparation of large-area synthetic diamond films on different substrates at a reasonable cost. An as-grown diamond film is terminated by hydrogen on the surface and shows hydrophobic wetting characteristics, besides chemical inertness. This has created problems for attachment of many biomolecules that are inherently hydrophilic. The challenge to make diamond useful for in vivo applications thus lies in covalently linking biomolecules to such surfaces. Several breakthroughs have been accomplished over the last decade, and attaching biomolecules to diamond in a controlled and reproducible way can nowadays be achieved in several different manners and is the focus of this article.

Boron-doped diamond electrodes have attracted increasing interest from researchers due to their outstanding properties for electroanalysis and other electrochemical applications. Material quality and availability have come a long way since the initial reports on the basic electrochemical properties back in the late 1980s and early 1990s. In this review, we highlight how diamond electrochemistry has diversified and matured in recent years in terms of the understanding of structure-property relationships and the development of new applications of materials in electroanalytical chemistry.