Scale-dependent microstructure and electronic transportation of Ni/Al-type nanomultilayers as a function of the bilayers number, the modulated ratio, and the periodicity were investigated. The deposited multilayers have anisotropic nanocrystalline structure and asymmetrical interfaces. This special interfacial feature is the result of asymmetrical diffusion of Ni to Al lattice near the Ni–Al interface. Anomalous resistivity enhancement increases with decreasing both the periodicity and the modulated ratio, but is insensitive to the number of bilayers. Accounting for the effects of grain boundary and interface boundary, the dominative mechanism at distinct length scales can be interpreted with the modified model of those of Fuchs–Sondheimer and Mayadas–Shatzkes. Especially for the thinnest film with smallest modulated ratio, the intermixing effect turns out to be the crucial mechanism in the electronic transportation of metallic nanomultilayers.

Highly aligned nanowire bundles were controllably fabricated through the reaction of Si with oxygen, using molten Ga and Au as catalysts. Scanning electron microscopy reveals that the bundles have the ability to self-assemble into various morphologies, a few of which, including one that strikingly resembles a sunflower, were not reported before. Examinations of the bundles by transmission electron microscopy show that they contain fine, amorphous SiOx nanowires, with x ranging from 1.2 to 1.5. In the sunflower-like morphology, highly packed bundles form the disc florets and loosely packed bundles around the rim of the disc form the ray florets. We have studied the conditions under which the sunflower-like morphology could be obtained and suggest a possible mechanism for its growth. Room-temperature cathodoluminescence spectra of the nanowire bundles show that they emit an intense broad-band light covering the entire visible range.

Hydrogenated In-doped ZnO (ZIO:H) films grown at different ratios, R, of hydrogen to argon were deposited at a substrate temperature of 100 °C for the organic light-emitting diodes (OLEDs). The OLEDs with the ZIO:H (R = 0.08) anode achieved a maximum luminance efficiency of 3.4 cd/A and a power efficiency of 0.6 lm/W, which are as good as the values of the control device fabricated on a tin-doped indium oxide (ITO) anode. This indicates that the efficiency of the OLEDs is critically affected by the ratio of injected hydrogen gas during the deposition of the ZIO and that the ZIO:H developed herein is promising as an alternative to conventional ITO.

In the present study, pure titanium (Ti) plates were firstly treated to form various types of oxide layers on the surface and then were immersed into simulated body fluid (SBF) to evaluate the apatite-forming ability. The surface morphology and roughness of the different oxide layers were measured by atomic force microscopy (AFM), and the surface energies were determined based on the Owens–Wendt (OW) methods. It was found that Ti samples after alkali heat (AH) treatment achieved the best apatite formation after soaking in SBF for three weeks, compared with those without treatment, thermal or H2O2 oxidation. Furthermore, contact angle measurement revealed that the oxide layer on the alkali heat treated Ti samples possessed the highest surface energy. The results indicate that the apatite-inducing ability of a titanium oxide layer links to its surface energy. Apatite nucleation is easier on a surface with a higher surface energy.

The long-duration oxidation behavior of a pressureless liquid-phase-sintered (LPS) α-SiC with 10 vol% Y3Al5O12 additives was studied by furnace oxidation tests in ambient air at 1100 to 1450 °C. The oxidation of this LPS SiC ceramic was found to be passive throughout these temperatures due to the formation of oxide scales, with a change in the oxidation behavior occurring at 1350 °C. It was also found that the oxidation behavior is very complex, exhibiting two distinct stages at all temperatures: (i) initial nonparabolic oxidation, where the rate-limiting mechanism is the outward diffusion of Y3+ and Al3+ cations from the secondary intergranular phase into the oxide scale with the activation energy of the oxidation being 504 ± 32 kJ/mol, followed by (ii) parabolic oxidation below 1350 °C, where the rate-determining mechanism is the inward diffusion of oxygen through the oxide scale with the activation energy being 310 ± 47 kJ/mol, or paralinear oxidation at and above 1350 °C, where oxidation is controlled by some mixed reaction/diffusion process. The existence of two oxidation regimes reflects the progressive crystallization of the oxide scale during the oxidation. Finally, guidelines are provided for the design and fabrication of low-cost, highly oxidation-resistant LPS SiC or other LPS nonoxide ceramics.

Luminescence properties of Yb-doped Ca-α-SiAlON phosphors with composition of Ca1−xYbxSi12−(m+n)Alm+nOnN16−n were investigated by using cathodoluminescence (CL). The ratio of Yb to Ca was kept constant while the host lattice was changed by replacing m+n(Si–N) bonds with m(Al–N) and n(Al–O) bonds. The luminescence of these phosphors consists of three peaks in the ultraviolet (UV), green (VIS), and infrared (IR) regions, which are attributed to the emissions from secondary phases, Yb2+ and Yb3+, respectively. The UV emission depends on the Si/Al ratio: the UV peak is centered at 310 nm for the Si-rich mix and at 360 nm for the Al-rich mix. We have found that Yb exists in the divalent state in α-SiAlON and in the trivalent state in the secondary phases.

Poly(amic acid) (PAA)–clay nacrelike composite films have been prepared by electrophoretic deposition of an emulsion of PAA, which was synthesized from pyromellitic dianhydride and 4,4′-dianminodiphenyl ether (ODA), containing various loadings of ODA-modified montmorillonite (MMT). The layered silicate was intercalated through reacting with PAA, and the ordered layered assembly of the PAA–MMT composite films was successfully accomplished, as conformed by Fourier transform infrared analysis and x-ray diffraction. The structural characterization of the films was supported by scanning electron microscopy, which displayed an ordered layered structure. The thermogravimetric analysis showed the content of the ODA-modified clay in PAA–MMT composite films that changed from 14.3 to 32.1 wt% and the improved thermal properties of the composite films. The mechanical properties of the composites were measured by tensile test. It was found that the modulus and strength of the composite films were greatly improved compared to those of the pure polymer film. An increment of about 155% in the modulus and 40% in the tensile strength were obtained from the composite films.

A polymer, which by pyrolysis transforms into Al–C–N–(O) ceramics, was synthesized from trimethylamine alane and cyan amide, and its applicability as a sintering additive for Si3N4 was investigated. Si3N4 powders were mixed with the precursor by treatment with organic slurries of the precursor to induce the homogeneous distribution of the additive. The green-bodies were pretreated in air or NH3 at 800 °C to control the chemical composition of the additive, through which the densification of Si3N4 could be improved. Dense samples with very fine grains (<2 μm) were obtained after sintering at 1600 °C in 0.1 MPa N2. Besides silicon nitride, submicrometer silicon carbide particles were observed in the samples, indicating that this procedure (i.e., the use of this novel sintering additive) also allows for the fabrication of SiC–Si3N4 composites.

An in situ surface-reaction approach has been developed for the synthesis of microcrystals Cu4I4(C6H5N)4, Cu4I4(C9H7N)4, and Cu2I2(C8H6N2) in solid films. Microcrystals of Cu4I4(C6H5N)4, Cu4I4(C9H7N)4, and Cu2I2(C8H6N2) were easily formed on a copper substrate at the solid Cu–liquid pyridine (C6H5N),–quinoline (C9H7N), and–quinoxaline (C8H6N2) interfaces. The resulting microcrystal films were characterized by photoluminescence spectroscopy, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, x-ray diffraction, and electrochemical impedance spectroscopy. The effect of ligands on the morphology of the film materials and their chemical properties were also discussed. These microcrystal films possessing reversible photocurrent and photovoltage properties were studied in detail. The photoactive and mechanically stable complex films described here may provide new strategies for fabricating photoluminescence solid films, photomodulation potential, and current films. The potential applications of the microcrystal films are for small light-induced electronic junction and photoluminescence sensors.

The mechanical behavior [i.e., stiffness, strength, and toughness (KIC)] of SiC Al–Si–Mg metal–ceramic composites (50:50 by volume) was studied at temperatures ranging from 25 to 500 °C. The SiC phase was derived from wood precursors, which resulted in an interconnected anisotropic ceramic that constrained the pressure melt-infiltrated aluminum alloy. The composites were made using SiC derived from two woods (sapele and beech) and were studied in three orthogonal orientations. The mechanical properties and corresponding deformation micromechanisms were different in the longitudinal (LO) and transverse directions, but the influence of the precursor wood was small. The LO behavior was controlled by the rigid SiC preform and the load transfer from the metal to the ceramic. Moduli in this orientation were lower than the Halpin–Tsai predictions due to the nonlinear and nonparallel nature of the Al-filled pores. The LO KIC agreed with the Ashby model for the KIC contribution of ductile inclusions in a brittle ceramic.

Fracture behavior of Zr55Cu30Al10Ni5 bulk metallic glass was investigated under quasi-static compression at strain rate of 10−4/s using an Instron testing machine and dynamic split Hopkinson bar (SHPB) compression with strain rate of about 1900–4300/s. Pronounced strain softening, especially past the peak stress, was observed under SHPB tests and compared with the distinct flow serrations under quasi-static tests. Scanning electron microscope revealed that the angle between the loading axis and major shear plane is less than 45°, deviating from the maximum shear stress plane. Microscopically, unlike the ordinary veinlike pattern found in quasi-static compression, the elongated veinlike pattern was observed at the onset position of rapid shearing under dynamic test. A closely arrayed dendritelike structure dominated the dynamic fracture, consequently, and should be the major pattern representing the rapid shear band propagation. In addition, a transition state from veinlike to dendritelike pattern was observed at the final instantaneous fracture region in quasi-static tests. Evidence revealed the characteristic dimension of dynamic fracture surface complies with Taylor’s meniscus instability criterion. The roles of free volume and adiabatic heating on the fracture strength and stress concentration on the fracture morphology are also discussed.

We studied the resistivity, photosensitivity, photoluminescence, and surface photovoltage of CdTe crystals doped with Ge or Sn to extend our knowledge of the influence of the deep-donor level on compensation and afterglow effects. We demonstrated a strong correlation between photosensitivity caused by photoelectrons with Fermi-level variations near the GeCd0/2+ or SnCd0/2+ energy levels. Surface photovoltage measurements confirmed that when the concentration of residual acceptors varied along the direction of growth, then trapping conditions dramatically changed as a defect was converted from a neutral state to doubly charged positive one.

By spark-eroding Fe75Si15B10 in water/ethanol mixtures, spherical particles with nanostructured cores consisting of mixed amorphous and crystalline phases were produced. The relative volume fractions of the amorphous and crystalline phases were dependent on the water/ethanol ratio. In the same process, continuous oxide layers were formed on the particle surfaces. The basic mechanisms responsible for the formation of the surface oxide layers and the core nanostructures were modeled. At frequencies ranging from 1 to 100 MHz, the combination of the core nanostructures and the insulating oxide shells yielded exceptionally low-loss magnetic behavior.

We report the fabrication of micron-sized rodlike particles of nonstoichiometric Co and Ni ferrites by aging coprecipitated Fe(OH)2 and M(OH)2—where M is either Ni or Co—at 90 °C in the presence of an external magnetic field (B ≈ 405 mT). Potassium nitrate was used as a mild oxidant. Resultant particles were analyzed by means of electron microscopy, x-ray powder diffraction (XRD), magnetometry, energy dispersive x-ray (EDX) spectrometry, and atomic absorption spectroscopy. Rodlike particles of both types of ferrite exhibited a relatively uniform thickness, an average aspect ratio close to 10, and have a spinel crystalline structure. EDX spectrometry and atomic absorption spectroscopy confirmed the incorporation of Ni2+ and Co2+ in the respective ferrite particles. The incorporation of Co2+ led to non-negligible remanence and coercivity. The incorporation of Ni2+ led to a lower saturation magnetization, whereas the remanence and coercivity of the Ni ferrite were very low, still typical of a soft ferrimagnetic material. The mechanism of formation of the rodlike particles was investigated by the time-dependent observation of growing Ni ferrite rods.

Dispersed uniform spherical silver particles were prepared in the absence of a protective colloid by rapidly mixing concentrated isoascorbic acid and silver-polyamine complex solutions. By varying the nature of the amine, temperature, concentration of reactants, silver/amine molar ratio, and the nature of the silver salt, it was possible to tailor the size of the resulting metallic particles in a wide range (80 nm to 1.3 μm). The silver spheres were formed by aggregation of nanosize subunits, the presence of which was detected by both electron microscopy and x-ray diffraction. Due to its simplicity, high metal concentration, and the absence of polymeric dispersants, the described method represents an advantageous route to manufacture cost-effectively dispersed uniform silver particles for electronic applications.

Stoichiometric silicon carbide coatings the same as those used in the formation of TRISO (TRistructural ISOtropic) fuel particles were produced by the decomposition of methyltrichlorosilane in hydrogen. Fluidized bed chemical vapor deposition at around 1500 °C, produced SiC with a Young’s modulus of 362 to 399 GPa. In this paper we demonstrate the deposition of stoichiometric silicon carbide coatings with refined microstructure (grain size between 0.4 and 0.8 μm) and enhanced mechanical properties (Young’s modulus of 448 GPa and hardness of 42 GPa) at 1300 °C by the addition of propene. The addition of ethyne, however, had little effect on the deposition of silicon carbide. The effect of deposition temperature and precursor concentration were correlated to changes in the type of molecules participating in the deposition mechanism.

Borides of high electron density metals such as Os show promise as hard materials. Arc-melting elemental osmium and boron under an argon atmosphere produced osmium diboride (OsB2). Both a Vickers diamond microindenter and a Berkovich nanoindenter were used to measure hardness. Vickers microindentation indicates that the hardness of OsB2 increases significantly with decreasing applied load. The average hardness reaches approximately 37 GPa as the applied load is lowered to 0.245 N. The hardness is found to be highly dependent on the crystallographic orientation. For the {010} grains, along the 〈100〉 direction, the average hardness is significantly higher than that in the orthogonal 〈001〉 direction. Cracks associated with pop-in events in the nanoindentation load–displacement curves are observed in the {010} grains. The measured Young’s modulus of OsB2 is 410 ± 35 GPa, which is comparable to that obtained from first-principles calculations.

Delamination at an interface with the weakest adhesion strength, which is found to be between the SiC(N) capping layer and the SiOCH low-k dielectric, is a potential failure mechanism contributing to time-dependent dielectric breakdown (TDDB) reliability. Bond breaking at that interface is believed to be driven by a field-enhanced thermal process and catalyzed by leakage current through the capping layer based on physical analyses and TDDB measurements. Delamination is found to be easier in terminated tips and corners than in parallel comb lines due to the layout orientation of the Cu lines. Moreover, TDDB activation energy Ea can be an indicator of the ease of delamination, whereby a lower Ea corresponds to an easier delamination.