Trace additions of boron to cast zirconium result in significant microstructural changes similar to those observed with additions of boron to titanium alloys. These changes include the promotion of dendritic growth and a refinement in both the prior β and α grain size. The refinement of the prior β grain size is explained using a model of grain refinement in association with values calculated from the binary Zr–B phase diagram. It is proposed that the refinement of the α phase occurs through a combination of increased nucleation and altered diffusion mechanisms during cooling through the β transus.

The physical and electrical properties of La2O3 with and without an Al2O3 capping layer deposited by remote plasma atomic layer deposition were investigated. The electrical properties of the La2O3 films degraded due to the formation of lanthanum hydroxide after being exposed to air. The results of x-ray photoemission spectroscopy showed that the quantity of OH groups absorbed increased after exposure to air. For La2O3 with an Al2O3 capping layer, however, the electrical properties of the film did not change substantially because the capping layer effectively suppressed the formation of lanthanum hydroxide. The capacitance of the La2O3 decreased more than 30% after exposure to air, while La2O3 with an Al2O3 capping layer decreased by only about 4%. The VFB value of the La2O3 with an Al2O3 capping layer was near zero, and the hysteresis was about 120 mV. The leakage current densities of the film were maintained below 5 × 10−7 A/cm2 up to −15 MV/cm and the effective breakdown field was about −23.5 MV/cm.

A new physical method is described for the preparation of metal microspheres by ultrasonic cavitation of low-melting point metals (<380 °C) immersed in hot silicone oil. The ultrasonic radiation causes dispersion of the molten metals into spheres, which solidify rapidly on cooling. This method is illustrated for the synthesis of Pb and Au–Si eutectic alloy.

In this study, we report the synthesis of uniform and narrowly size-distributed ZnO nanoparticles with sizes of approximately 3 nm; the nanoparticles were prepared by means of organic-ligand-assisted hydrothermal conditions with various organic modifiers. The results obtained herein revealed that among the various functional groups tested (alcohols, aldehydes, carboxylic acids, and amines), only hexanol effectively controlled the nucleation and crystal growth of spherical ZnO nanoparticles. The use of hexanol also caused the surface of the ZnO particles to change from hydrophilic to hydrophobic, which would enhance the dispersion of these particles in polymer matrices, paints, cosmetics, and other organic application media.

The influence of high magnetic field on nitriding behavior was investigated in a mixture of NH3 and H2. It was found that high magnetic field could shift the equilibrium of nitriding reaction; this proved that the critical nitrogen potential to form γ′-Fe4N and ε-Fe3N phase was evidently enhanced compared with conventional nitriding. This research provides a new approach for a selective nitriding process.

Inks containing silver nanoparticles of 12 nm, 80 nm, and a 15%/85% mixture of the two sizes were used to evaluate the effect of particle size and size distribution on the electrical properties of sintered films. The silver layers deposited with a “drop-on-demand” inkjet printer were heated at temperatures ranging from 125 to 200 °C. The small particles formed less resistive films at 125 °C, while the larger ones provided better electrical conductivity above 150 °C. The inks containing mixed small and large particles yielded the most conductive silver films over the entire investigated temperature range. A mechanism explaining these results is proposed based on the evolution of film microstructure with temperature.

The interfacial reactions in Sn-0.7wt%Cu/ENIG SUS304 couples at 240, 255, and 270 °C are examined in this study. The Ni-containing ternary Cu6Sn5 phase is formed at the Ni/liquid interface in the early reaction stage then it detaches massively from the SUS304 substrate and splits into two layers in the molten solder as the reaction time increases. This phase finally disintegrates and disappears. The square pillar-shaped FeSn2 phase is found on top of the SUS304 substrate when the Cu6Sn5 layer detaches. The reaction phase formation, detachment, and split mechanisms are proposed. The spalling phenomenon is reviewed and discussed. The growth mechanism of the FeSn2 phase obeys the parabolic law, and the activation energy is determined to be 112.5 KJ/mol.

A new low sintering temperature microwave dielectric ceramic, Li2ZnTi3O8, was investigated. X-ray diffraction data show that Li2ZnTi3O8 has a cubic structure [P4332(212)] with lattice parameters a = 8.37506 Å, V = 587.44 Å3, and Z = 4 when the sintering temperature is 1050 °C. The Li2ZnTi3O8 ceramic exhibits good microwave dielectric properties with εr about 26.2, Q×f value about 62,000 GHz, and τf about −15 ppm/°C. The addition of BaCu(B2O5) can effectively lower the sintering temperature from 1050 to 900 °C without degrading the microwave dielectric properties. Compatibility with Ag electrode indicates this material can be applied to low temperature cofired ceramic devices.

The fabrication and properties of fiber metallic glass laminates (FMGL) composite composed of Al-based metallic glasses ribbons and fiber/epoxy layers were reported. The metallic glass composite possesses structural features of low density and high specific strength compared to Al-based metallic glass and crystalline Al alloys. The material shows pronounced tensile ductility compared to monolithic bulk metallic glasses.

We describe progress in understanding the effect of simulated chemical-mechanical planarization (CMP) slurry chemistry on the evolution of defects and formation of damage that occurs during CMP processing. Specifically, we demonstrate the significant effect of aqueous solution chemistry on accelerating crack growth in porous methylsilsesquioxane (MSSQ) films. In addition, we show that the same aqueous solutions can diffuse rapidly into the highly hydrophobic nanoporous MSSQ films containing interconnected porosity. Such diffusion has deleterious effects on both dielectric properties and the acceleration of defect growth rates. Crack propagation rates were measured in several CMP solutions, and the resulting crack growth behavior was used to qualitatively predict the extent of damage during CMP. These predictions are compared with damage formed during actual CMP processes in identical chemistries. We discuss the effects of both the high and low crack growth rate regimes, including the presence of a crack growth threshold, on the predicted CMP damage. Finally, implications for improved CMP processing were considered.

The parallel nano-scanning calorimeter (PnSC) is a silicon-based micromachined device for calorimetric measurement of nanoscale materials in a high-throughput methodology. The device contains an array of nanocalorimeters. Each nanocalorimeter consists of a silicon nitride membrane and a tungsten heating element that also serves as a temperature gauge. The small mass of the individual nanocalorimeters enables measurements on samples as small as a few hundred nanograms at heating rates up to 104 K/s. The sensitivity of the device is demonstrated through the analysis of the melting transformation of a 25-nm indium film. To demonstrate the combinatorial capabilities, the device is used to analyze a Ni–Ti–Zr sample library. The as-deposited amorphous samples are crystallized by local heating in a process that lasts just tens of milliseconds. The martensite–austenite transformation in the Ni–Ti–Zr shape memory alloy system is analyzed and the dependence of transformation temperature and specific heat on composition is revealed.

High-capacity thin-film germanium was coupled with free-standing single-wall carbon nanotube (SWCNT) current collectors as a novel lithium ion battery anode. A series of Ge–SWCNT compositions were fabricated and characterized by scanning electron microscopy and Raman spectroscopy. The lithium ion storage capacities of the anodes were measured to be proportional to the Ge weight loading, with a 40 wt% Ge–SWCNT electrode measuring 800 mAh/g. Full batteries comprising a Ge–SWCNT anode in concert with a LiCoO2 cathode have demonstrated a nominal voltage of 3.35 V and anode energy densities 3× the conventional graphite-based value. The higher observed energy density for Ge–SWCNT anodes has been used to calculate the relative improvement in full battery performance when capacity matched with conventional cathodes (e.g., LiCoO2, LiNiCoAlO2, and LiFePO4). The results show a >50% increase in both specific and volumetric energy densities, with values approaching 275 Wh/kg and 700 Wh/L.

We report temperature-dependent electrical resistivity (or dc conductivity, σdc) down to 4 K for pristine and gamma-irradiated microwave plasma-assisted chemical vapor-deposited boron-doped diamond films with [B]/[C]gas = 4000 ppm to gain insights into the nature of conduction mechanism, distribution, and kinetics of point defects generated due to gamma irradiation prompted by the article [Gupta et al., J. Mater. Res.24, 1498 (2009)]. The pristine samples exhibit typical metallic conduction up to 50 K and with reduction in temperature to 25 K, the σdc decreases monotonically followed by saturation at 4 K, suggesting “disordered” metal or “localized” behavior. For irradiated films, continuous increasing resistivity with decreasing temperature demonstrates semiconducting behavior with thermal activation/hopping conduction phenomena. It is intriguing to propose that irradiation leads to substantial hydrogen redistribution leading to unexpected low-temperature resistivity behavior. Scanning tunneling microscopy/spectroscopy helped to illustrate local grain and grain boundary effects.

Structural origin of the high glass-forming ability (GFA) in multicomponent bulk metallic glasses (BMGs) caused by minor alloying was investigated using state-of-the-art synchrotron radiation techniques. It is found that a two-shell icosahedral cluster with one Y center is the basic structural unit in the representative Cu46Zr42Al7Y5 BMG, which may be densely packed with the help of shared and glue atoms, leading to enhanced ordering at short and medium range. This cluster dense packing may play a key role in achieving the high GFA in CuZrAlY alloy, which also explains the strong dependence of GFA on Y content observed in many experiments. The present work may be extended to a series of multicomponent amorphous alloys, the formation of which is strongly dependent on minor alloying.

Phase-pure nanostructured WB ceramics are hot pressed at ultrahigh pressures of 1.0 to 3.0 GPa and high temperatures of 700 to 1000 °C (UHPHT) for 60 min. The UHPHT samples are nanograin size from 15 to 40 nm. Our experimental observation shows that ultrahigh pressure could improve densification, and the density of WB samples could reach 99.4% of theoretical. The comparative experiments carried out at ambient pressure and temperatures of 550 to 1100 °C for 60 min indicate that the external pressure was favorable for phase-pure and highly dense WB formation. In addition, the UHPHT samples give a high hardness value of 28.9 ± 0.8 GPa.

Two novel La3+ and Ti4+ cosubstituted Sr3LaNb3O12 ceramics, Sr2La2TiNb2O12 and SrLa3Ti2NbO12, were prepared and the effect of substitution on the microwave dielectric properties was investigated. Results showed that as the amounts of substitution increased, dielectric constant (εr) increased from 36 to 41, and temperature coefficient of resonant frequency (τf) improved from −9 to 3 ppm/°C, whereas the quality factor (Q×f) decreased from 45,000 to 33,600 GHz. A temperature-stable microwave dielectric ceramics SrLa3Ti2NbO12 with τf of 3 ppm/°C, εr of 41, Q×f of 33,600 GHz was obtained; it might be a promising candidate for practical application in base stations if the quality factor is enhanced beyond 40,000 GHz.

The microstructures of two pressureless sintered ceramics, ZrB2 and HfB2 with 20 vol% MoSi2 added, were analyzed by scanning and transmission electron microscopies. Carbides and oxides of the transition metals and MoB were observed to be well dispersed within the boride matrix. Mo5Si3 and Mo5SiB2, with Zr or Hf impurities, were observed at triple grain junctions and showed a partial wetting of the matrix. It was also noticed that the borides had a core-shell structure, which was especially pronounced in the ZrB2-based composite. The experimental results suggest the formation of a Mo–Si–B liquid phase at high temperature, which strongly promoted the densification. The densification mechanisms are discussed in light of the microstructure evolution on sintering, thermodynamic considerations, and the phase diagrams of the species involved.

Cr3+-doped LiInSiO4 phosphors were prepared by a solid-state reaction method. X-ray diffraction measurement was carried out for crystalline phase identification. Absorption, photoluminescence, excitation, and time-resolved spectra were measured to investigate the optical properties of the phosphors. Two broadband near-infrared emissions centered at 920 and 1172 nm were observed. Time-resolved spectra show that the emission at 1172 nm decays more quickly than the emission at 920 nm. The electron spin resonance spectra exhibit a broad resonance signal at g = 1.96 because of exchange-coupled Cr3+ pairs. The value of Dq/B for low and intermediate crystal fields was evaluated. We suggest that Cr3+ incorporated into different octahedral sites of the crystal is responsible for the different near-infrared luminescence.

Aiming to bind molecules without O-containing groups such as the –OH or –COOH functional groups, a new two-step method involving thermal activation and followed by an in situ chemical reaction was suggested, and the binding of the pyridine molecule on TiO2 nanocrystalline films was realized. UV-Vis, FTIR, and XPS characterizations revealed that pyridine molecules are chemically linked to the TiO2 surface by forming Ti-pyridine bonds. Mott-Schottky measurements indicated that the binding of pyridine results in a positive shift of the flat band potential for TiO2 nanocrystalline film, which is attributed to the alternating surface dipole moment of TiO2 nanocrystals upon pyridine binding. Electrochemical and photoelectrochemical investigations indicated that the binding of pyridine on TiO2 nanocrystalline film has high electrochemical and photoelectrochemical stability.

Applying the glass fluxing method, a peritectic Fe–Ni alloy with a composition of Fe–4.35 at.% Ni was undercooled. It was found that when the initial melt undercooling (ΔT) is smaller than 130 K, the overall thickness of the peritectic phase formed in peritectic reaction (PR) and peritectic transformation (PT) decreases as ΔT increases. The nonequilibrium effects of the primary solidification on PR and PT in the undercooled peritectic Fe–Ni alloys were illuminated. With increasing ΔT, since the driving forces for PR and PT change slightly, the decrease of the overall thickness of the peritectic phase formed in PR and PT can be mainly ascribed to the reduced transformation time for PT.