Sol–gel spin coating is applied to fabricate the pure and different concentrations of aluminum (Al)-doped ZnO films on high-quality silicon substrates. All films are showing high crystallinity in X-ray diffraction study, and lattice constants were obtained using PowderX software. The value of crystallite size was found in range of 20–40 nm. EDX/SEM mapping was performed for 2 wt% Al-doped ZnO film, which shows the presence of Al and its homogeneous distribution in the film. SEM investigation shows nanorods morphology all over the surface of films, and the dimension of nanorods is found to increase with Al doping. The E(g)dire. values were estimate in range of 3.25–3.29 eV for all films. Linear refractive index was found in range of 1.5–2.75. The χ1 value is found in range of 0.13–1.4 for all films. The χ3 values are found in range of 0.0053 × 10−10 to 6.24 × 10−10 esu for pure and doped films. The n2 values were also estimated. These studies clearly showed that the properties of ZnO have been enriched by Al doping, and hence doped films are more appropriate for optoelectronic applications.

In this investigation, we have reported the alloying behavior, phase evolution, and thermal stability of equiatomic AlCoCrFeNiTi high-entropy alloy (HEA). The 40 h milled powder shows good chemical homogeneity with agglomerated particles varying in the range of ∼3–18 μm. The formation of a nanostructured single-phase BCC (a = 2.85 ± 0.01 Å) was observed along with the minor tungsten carbide (WC) phase that formed due to contamination during milling. Thermal stability of the alloy has been studied using dynamic differential scanning calorimetry (DSC) thermogram and in situ X-ray diffraction. It has been found that this HEA is stable up to 600 °C (873 K). Consolidated samples at 1000 °C (1273 K) showed the transformation of body centered cubic (BCC) phase into the B2 (a = 2.87 ± 0.03 Å) phase co-existing with minor hexagonal WC (a = 2.90 Å, c = 2.83 Å) phase.

A kind of novel Ni–P gradient coating/stannate conversion film was deposited on AZ91D magnesium alloy (AZ91D alloy) by an integrative method involved stannate conversion and electroless plating. The results indicated that using sodium hypophosphite concentrations varied as 5, 10, 22, 46, and 60 g/L in the bath, the electroless Ni–P gradient coating with typical cell morphologies was successfully prepared, and the structures transited from crystalline → microcrystalline → amorphous were obtained as increasing P content from 3.31 to 12.58 wt%. Furthermore, the corrosion morphologies, polarization curves, and the electrochemical impedance spectroscopy result indicated that the corrosion resistance of AZ91D alloy substrate was significantly improved and the corrosion resistance of Ni–P gradient coating was superior than that of stannate conversion film, which might be attributed to the gradient structure and rising P content with unique function.

AlCoCrFeNi is among the promising high-entropy alloys (HEAs) that possess high strength with considerable ductility. Powder sintering is one of the competitive routes for the production of HEA powders. However, sintering of HEA powders under a pressureless condition is difficult. The present work aims to produce high-density components from mechanically alloyed AlCoCrFeNi HEA powders through the pressureless sintering method. Nearly full density was achieved at 1275 °C. Sintering was performed in the presence of a viscous phase in the temperature range of 1200–1250 °C, which was confirmed through differential scanning calorimetry and dilatometric measurements. This viscous phase was found have a Cr-rich composition, detected by interrupting the sintering and quenching of the sample. The powder initially contained the BCC phase with a small fraction of FCC and other phases. During sintering, a significant fraction of the FCC phase and nanosized B2 phase were formed. Sintered sample had a hardness of 679 ± 20 Hv.

Surface water can affect the properties of metal oxide nanoparticles. Investigations on several systems revealed that nanoparticles have different thermodynamic properties than their bulk counterparts due to adsorbed water on their surfaces. Some thermodynamically metastable phases of bulk metal oxides become stable when reduced to the nanoscale, partially due to interactions between high energy surfaces and surface water. Water adsorption microcalorimetry and high-temperature oxide melt solution calorimetry, low-temperature specific heat calorimetry, and inelastic neutron scattering are used to understand the interactions of surface water with metal oxide nanoparticles. Computational methods, such as molecular dynamics simulations and density functional theory calculations, have been used to study these interactions. Investigations on titania, cassiterite, and alumina illustrate the insights gained by these measurements. The energetics of water on metal oxide surfaces are different from those of either liquid water or hexagonal ice, and there is substantial variation in water interactions on different metal oxide surfaces.

The kinetics of silica polymerization was measured in silicic acid solutions containing a suite of 0.1 M amino acids, 0.1 M citric acid, 0.7 M NaCl, and 0.10 M NaCl (Control). Fitting a modified classical rate model to measurements of induction time (τ) at 20 °C for a series of supersaturated solutions, we estimate the thermodynamic barrier (ΔGc), interfacial free energy (γ), and kinetic barrier (Δagk) for silica nucleation. For 0.10 M NaCl solutions, γControl = 54.9 ± 1.6 mJ/m2 and ΔagkControl = 2.29 × 10−19 J/mol. These values are consistent with previous reports for amorphous and fused silica materials. To facilitate comparisons with the treatments, ΔagkControl is converted to a molar basis and used as a reference datum, such that ΔagkControl = 0.0 J/mol. The effects of salt and organic acids on nucleation rate have thermodynamic and kinetic origins, respectively. Faster nucleation rates measured in 0.7 M NaCl solutions arise from a lower interfacial free energy, such that γ0.7 M NaCl = 51.4 ± 1.7 mJ/m2. Organic acids increase rate through biomolecule-specific reductions in Δagk. Catalytic effects are greatest for lysine (Δagklysine = −1685 ± 315) and citric acid (Δagkcitric = −1690 ± 96 J/mol). Reductions in the kinetic barrier correlate with net positive charge of the amino acids and dissociation of the amine $\left( {{K_{\alpha {\rm{ ‐ N}}{{\rm{H}}_3}^ {\bf{+}} }}} \right)$ group and thus the abundance of the conjugate base. Citric acid, lacking amine groups, promotes the greatest rate enhancement, thus demonstrating the role(s) of additional kinetic factors in promoting nucleation rate. Catalytic activity correlates with multiple physical and chemical properties of the organic acids.

Bainite transformation in steels is influenced by various factors. In the present work, bainite transformation in medium carbon high alloyed steel was investigated focusing on the influence of preexisting VC carbides on the morphology and transformation kinetics of the subsequently formed bainite. Hot-work die steels were held at 950 °C for various times to precipitate VC carbides, then rapidly cooled from 950 to 350 °C and held at this temperature for the bainite transformation. It is found that the bainite transformation was obviously accelerated by the preexisting VC carbides precipitated at the austenite region. The precipitation of carbides leads to a decrease in carbon concentration in the matrix, which decreases the effective activation energy and increases the highest temperature for the nucleation of bainite. Besides, bainite was observed to grow beside the VC carbides. It suggests that the VC carbides in the matrix act as nucleation sites for the bainite transformation. In the specimens, the bainite transformation is accelerated, and a higher fraction of bainite is formed when there are carbides in the matrix.

Process parameters (laser power and scanning speed) for H13 steel specimens produced by selective laser melting (SLM) are optimized, and microstructural characteristics and mechanical properties are investigated. The optimum process parameters are a laser power of 170 W and a scanning speed of 400 mm/s according to the maximum relative density of 99.2%. The microstructure consists of cellular grains and columnar crystal, which are composed of lath martensite and retained austenite, and there are no carbides or other second-phase particles present. The size of cellular grains is 1 μm. Compared with the common processed (forged and heat-treated) H13, SLM H13 has similar microhardness (561 HV) and tensile strength (1909 MPa) values. However, the elongation (12.4%) is a factor of ∼3 times higher and the impact energy (14.4 J) of the SLM specimen is somewhat lower. The relationship between the microstructure and mechanical properties is discussed. Fine grains and no second-phase precipitation determine the strength and plasticity of SLM samples.

Oligodepsipeptides (ODPs) with alternating amide and ester bonds prepared by ring-opening polymerization of morpholine-2,5-dione derivatives are promising matrices for drug delivery systems and building blocks for multifunctional biomaterials. Here, we elucidate the behavior of three telechelic ODPs and one multiblock copolymer containing ODP blocks at the air–water interface. Surprisingly, whereas the oligomers and multiblock copolymers crystallize in bulk, no crystallization is observed at the air–water interface. Furthermore, polarization modulation infrared reflection absorption spectroscopy is used to elucidate hydrogen bonding and secondary structures in ODP monolayers. The results will direct the development of the next ODP-based biomaterial generation with tailored properties for highly sophisticated applications.

Direct determination of barrier height (ΦBH) value between Ir and single crystal (001) hydrogen-terminated diamond with lightly boron doped has been performed using x-ray photoelectron spectroscopy technique. 70 nm Ir islands were formed on hydrogen-terminated diamond surface using anodic aluminum oxide. The ΦBH value for Ir/hydrogen-terminated diamond was −0.43 ± 0.14 eV, indicating that Ir was a suitable metal for ohmic contact with hydrogen-terminated diamond. The band diagram of Ir/hydrogen-terminated diamond was obtained. The experimental ΦBH was compared with the theoretical ΦBH in this work.

Ternary Al–15 wt% Cu–7 wt% Si and Al–22 wt% Cu–7 wt% Si alloy specimens were generated by transient directional solidification (DS) and rapid solidification (RS) techniques. The microstructures are constituted by an α-Al dendritic matrix surrounded by two eutectic, that is, a binary eutectic (Si + α-Al) and a bimodal eutectic, consisting of cellular-type binary eutectic colonies (α-Al + Al2Cu) in a ternary eutectic matrix consisting of α-Al + Al2Cu + Si. The bimodal eutectic exists at cooling rates from 0.5 to 250 K/s. The secondary dendritic spacing, λ2, of the DS samples varied from 5 to 20 μm and from 10 to 18 μm for both examined alloys. The λ2 from 2.7 to 4.0 μm characterized the RS samples. Mechanical properties have been determined for various samples related to different dendritic spacing values. Based on the evaluation of the rapidly solidified microstructures, it was possible to assess the cooling rates.

Recent molecular dynamics simulations revealed that 〈c + a〉 dislocations in Mg were prone to dissociation on the basal plane, thus becoming sessile. Basal dissociation of 〈c + a〉 dislocations is significant because it is a major factor in the limited ductility and high work-hardening in Mg. We report an in situ transmission electron microscopy study of the deformation process using an H-bar-shaped thin foil of Mg single crystal designed to facilitate 〈c + a〉 slip, observe 〈c + a〉 dislocation activity, and establish the validity of the largely immobile 〈c + a〉 dislocations caused by the predicted basal dissociation. In addition, through detailed observations on the fine movement of some 〈c + a〉 dislocations, it was revealed that limited bowing out movement for some non-basal portions of 〈c + a〉 dislocations was possible; under certain circumstances, i.e., through attraction and reaction between two 〈c + a〉 dislocations on the same pyramidal plane, at least portions of the sessile configuration were observed to be reversed into a glissile one.

With rapid growth of human population and decreasing labefaction of our environment, the usable fresh water is facing severe pollution and global shortage. Bio-inspired engineering and biotemplate-directed engineering thus offer great promise in clean water generation, including desalination, decontamination, and disinfection. This perspective begins with an introduction of solar energy-based interfacial evaporation system inspired by the natural systems of organisms, and then provides a review of the development and recent progress of the interfacial evaporation system for clean water generation. The long-term outlook in this field of clean water generation using bio-inspired interfacial systems is also discussed.

Deformation twinning has been frequently observed in body-centered cubic (BCC) high entropy alloys (HEAs), however, the underlying mechanism remains elusive. We perform molecular dynamics simulations on a representative BCC HEA nanopillar under high-symmetry compression, describe atomic details of deformation twinning, and propose a mechanism of twin nucleation from the surface. We find that twinned regions are formed by partial dislocations and that chemical heterogeneity can reduce local fault energy and promote stacking faults and twins. These results help to understand the propensity for stacking fault formation and twinning in HEAs and may guide the design of novel HEAs through control of active twinning mechanisms.

To understand the effect of pH value on the corrosion and corrosion fatigue behavior of AM60 magnesium alloy, electrochemical tests, viz., electrochemical impedance spectroscopy (EIS) and fatigue tests, were carried out in PBS (phosphate buffered saline) solutions of pH 5.2, 7.4, and 9.0. The microstructure was investigated by scanning electron microscopy (SEM). Results are as follows: (i) the corrosion mechanism of AM60 under different pH values was different according to EIS; (ii) the corrosion resistance and corrosion fatigue life reduced in the following order: pH 9.0 > pH 7.4 > pH 5.2; (iii) the crack initiation was associated with hydrogen embrittlement of AM60 on the basis of fractographic analysis.

Ambient water condenses readily on metal oxides, which can lead to water film formation and water-mediated reactions at the oxide surface. Similar to bulk water, thin water films with thicknesses below 10 molecular layers can modify the oxide surface chemical reactivity and stability. However, due to the confinement of mass transport at the oxide surface, these processes do not proceed exactly as they do in bulk liquid water. In this review article, we will present selected examples from our group and others’ that illustrate the rich interaction of MgO and TiO2 nanostructures with thin water films. We will show that these condensed water films can induce significant chemical, structural, and microstructural transformations of metal oxide nanostructures such as dissolution/precipitation, morphological changes, crystallization, and self-assembly in the solid state.