Age-hardening behavior of a new generation of FeCo alloys [Fe–40Co–5V–0.005B–0.015C–0.5Mo–0.5Nb (at.%)] is characterized by microhardness, tensile testing, electrical resistivity, and magnetic properties. The alloy exhibits maximum hardening when aged at 600 °C. Precipitation of γ2 (V-rich face-centered cubic phase) during aging appears to be responsible for the observed hardening behavior. The alloy exhibits superior creep resistance when subjected to solutionizing in γ phase field and aged at 600 °C. On the other hand, the room temperature tensile ductility of the aged alloy depends on the grain size, which in turn can be controlled by varying the solutionizing condition. The age-hardened alloy exhibits a room temperature electrical resistivity of 70–75 μΩ cm. The higher resistivity of the present alloy as opposed to the commercial FeCo–2V alloys is attributed to the high V content of the alloy. Structure-sensitive magnetic properties like coercivity and core losses of the alloy are affected by the aging treatment, and the maximum coercivity is observed when the alloy is aged at 600 °C. High coercivity of the alloy is attributed to the fine distribution of paramagnetic γ2 precipitate, fine grain size, and internal stress arising from phase transformation.

A thin-frame nano-network film of titania with backbone diameter of 20–30 nm was obtained from precursor templating of nano-porous polymer with nano-channels 50 nm in width. The nano-porous polymer templates were prepared by selective removal of the polyisoprene (PI) domain with ozone from the bicontinuous structure formed through blending a symmetric polystyrene-block-polyisoprene (PS-b-PI) copolymer with a PS homopolymer (h-PS). The titania network possessed the preferred anatase crystallinity for photocatalytic applications and a specific surface area of 53 m2/g, comparable to that of Degussa P25, a widely used commercial photocatalyst. Photocatalytic performance of the fractured titania network film was also comparable to that of Degussa P25 in both gas-phase NO oxidation and liquid phase methylene blue degradation. The much larger overall structure size of the fractured titania network film, however, offers advantages over the nano-particulate form of P25, namely, easy handling and rapid recycling from treated streams.

Y0.9Ba1.9La0.2Cu3Oy (La-YBCO) thin films were prepared by an off-axis magnetron sputtering method on MgO substrates with and without a BaZrO3 buffer layer. Insertion of BaZrO3 buffer layer was effective for obtaining La-YBCO films with pure c-axis orientation and in-plane alignment at low temperatures below 600 °C. We prepared La-YBCO thin films on BaZrO3-buffered MgO substrates using a temperature-gradient method, in which a template La-YBCO layer was first deposited at 600 °C, and then the temperature was continuously raised to 700 °C. By this method, La-YBCO thin films with improved crystallinity were successfully prepared. It was also proved that the insertion of the BaZrO3 buffer layer enables us to prepare high-quality La-YBCO films with high reproducibility.

The electrical properties of ultrathin amorphous Al2O3 films, grown by low temperature metal-organic chemical vapor deposition from aluminum(III) 2,4-pentanedionate and water as co-reactants, were examined for potential applications as gate dielectrics in emerging complementary metal-oxide semiconductor technologies. High-frequency capacitance–voltage and current–voltage techniques were used to evaluate Al2O3 films deposited on silicon oxynitride on n-type silicon (100) substrates, with thickness ranging from 2.5 to 6.5 nm, as a function of postdeposition annealing regimes. Dielectric constant values ranging from 11.0 to11.5 were obtained, depending on the annealing method used. Metal-insulator-semiconductor devices were demonstrated with net equivalent oxide thickness values of 1.3 nm. Significant charge traps were detected in the as-deposited films and were mostly passivated by the subsequent annealing treatment. The main charge injection mechanism in the dielectric layer was found to follow a Poole–Frenkel behavior, with post-annealed films exhibiting leakage current an order of magnitude lower than that of equivalent silicon oxide films.

In this work, the effect of a sol-gel ZrO2–3 mol% Y2O3 thin film on the fracture properties of a variety of brittle substrates was investigated. The results suggest that the film does not have any appreciable influence on the fracture behavior of crystalline substrates but dramatically affects the fracture properties of amorphous layers. In particular, a significant reduction of average fracture strength and a major increase of the Weibull modulus were observed on coated glassy slides. The origin of such variations is attributed to the generation of a homogeneous flaw population in the vitreous substrates, and the possible mechanisms for the production of flaws are analyzed. Implications of these results for the practical use of coated glassy layers are discussed.

The structural characteristics of silver nanoparticles embedded in glass by various routes of fabrication were studied in detail using high-resolution electron microscopy to find out if they are influenced by interaction with the surrounding glass matrix. Besides the formation conditions, the strength of the interaction between metal and glass governs the size-dependent changes of lattice spacings in such nanoparticles. However, determination of these changes is not straightforward because of complicated particle configurations and the interference nature of the lattice imaging technique. Imaging of lattice plane fringes and careful diffractogram analysis allowed the exclusion of any kind of tetragonal lattice distortion or transformation to hexagonal lattice type that may be deduced at first sight. Instead, the formation of twin faults in these nanoparticles turned out to be the essential structural feature and the main source of confusion about the lattice structure observed. The variety of particle forms is comparable to particles supported on oxide carriers. It is composed of single-crystalline particles of nearly cuboctahedron shape, particles containing single twin faults, multiple twinned particles containing parallel twin lamellae, and multiple twinned particles composed of cyclic twinned segments arranged around axes of 5-fold symmetry. The more twin planes involved in the particle composition, the more complicated is the interpretation of lattice spacings and lattice fringe patterns due to superposition of several twin segments.

The coarsening behavior of the Pb-rich phase particles in 63Sn–37Pb (wt%) solder was investigated following isothermal annealing treatments. Samples were exposed to cooling rates of 0.1, 1.0, 10, and 100 °C/min. Annealing temperatures were 25, 55, 70, 85, and 100 °C, and times were 2–100 days. The mean particle diameter decreased from 1.8 × 10−3 to 0.8 × 10−3 mm with increased cooling rate, indicating two solidification regimes: one for cooling rates ≤1 °C/min and the other for cooling rates of ≥10 °C/min. The Pb-rich phase particles coarsened more quickly in samples made at the two fastest cooling rates. There was little Pb-rich phase particle coarsening at 25 and 55 °C for all annealing times. Coarsening rate kinetics were examined specifically for the 10 and 100 °C/min data using the expression Atnexp[−ΔH/RT]. The values of n were 0.23 ± 0.11 and 0.36 ± 0.13, respectively; n was not sensitive to annealing temperature. The corresponding 1/n values indicated that the coarsening mechanism changed from a fast diffusion to a bulk diffusion controlled process with a faster cooling rate. The apparent activation energy ΔH ranged from 16 ± 8 to 41 ± 8 kJ/mol; the values increased with cooling rate from 10 to 100 °C/min. The ΔH value was sensitive to annealing temperature only for the faster cooling rate of 100 °C/min. Together, the n and ΔH values indicated that an accelerated, fast diffusion mechanism with low activation barriers characterized the Pb-rich phase coarsening in samples exposed to a slower cooling rate, greater annealing, or a combination of the two conditions. That mechanism likely originated from the in situ development of recover/recrystallization microstructures in the Sn-rich phase. At faster cooling rates, those microstructures were not as well developed, so coarsening was controlled more by the higher activation barriers of bulk diffusion processes.

The thermal degradation behavior of indium tin oxide (ITO) thin films coated on glass substrates using radio frequency (rf) magnetron sputtering was investigated over the temperature range of 100–400 °C in air. The resistivity of ITO films increases abruptly after the thermal degradation temperature of 250 °C is reached, with a slight increase from 200 to 250 °C. The x-ray photoelectron spectrometry intensity ratio of O/(In + Sn) in thermally degraded ITO films is higher than that in normal films. The carrier concentration gradually decreases up to 200 °C, sharply drops between 200 and 250 °C with increasing temperature, and then saturates from 275 °C. The Hall mobility drops suddenly at 275 °C. The diffusion of oxygen into oxygen interstitials and oxygen vacancies and the chemisorption of oxygen into grain boundaries decrease the carrier concentration and the Hall mobility, respectively. The former mainly affects the resistivity of ITO films below 250 °C, and the later above 250 °C.

A new type of bearing alloy containing ultrafine sized tin and silicon dispersions in aluminum was designed using laser surface alloying and laser remelting techniques. The microstructures of these non-equilibrium processed alloys were studied in detail using scanning and transmission electron microscopy. The microstructures revealed three distinct morphologies of tin particles namely elongated particles co-existing with silicon, globular particles, and very fine particles. Our detailed analyses using cellular growth theories showed that the formation of these globular tin particles was due to the pinching off of the tin rich liquid in the inter-cellular space by the growth of aluminum secondary dendrite arms. Evidence of fine recrystallized aluminum grains at the top layer due to constrained solidification was shown. Thermal analyses suggested that melting of the spherical shaped tin particles was controlled by the binary aluminum-tin eutectic reaction, whereas non-spherical tin particles melted via the tin-silicon eutectic reaction.

A NiFe2O4 particle/organic hybrid was synthesized in situ from iron-organic and nickel organic compounds below 100 °C. A mixture of nickel (II) acetylacetonate (NA) and iron (III) 3-allylacetylacetonate (IAA) was hydrolyzed and polymerized yielding spinel oxide particle/oligomer hybrid. X-ray diffraction analysis revealed that the crystallinity of spinel particles was dependent upon the hydrolysis conditions of NA-IAA. Nanocrystalline nickel ferrite particles around 10 nm were uniformly dispersed in the organic matrix. The formation of nickel ferrite was confirmed by energy-dispersive x-ray and x-ray photoelectron spectroscopy. The saturation magnetization of hybrid increased with increasing water amount for hydrolysis. Nano-sized nickel ferrite particle/organic hybrid showed a BH curve with no remanence above 75 K. The magnetization versus H/T curves at 300, 200, and 75 K were superimposed on the same curve and satisfied the Langevin equation. The remanent magnetization and coercive field of the hybrid were 7.4 emu/g and 460 Oe, respectively, at 5 K.

A five-step indentation scheme is proposed to extract the elastic and viscoelastic properties of polymeric materials using a sharp indenter. In the formulation, analytical solutions to the elastic-viscoelastic deformation based on the concept of “effective indenters” proposed by both Pharr and Bolshakov [Understanding nanoindentation unloading curves. J. Mater. Res.17, 2660 (2002)] and Sakai [Elastic recovery in the unloading process of pyramidal microindentation. J. Mater. Res.18, 1631 (2003)] were derived. Indentation experiments on polymethylmethacrylate following the five-step scheme were performed. The elastic-viscoelastic parameters were extracted by fitting the solution based on Sakai’s effective indenter to the experimental results using a genetic algorithm. It was found that the solution based on Sakai's effective indenter was able to correctly extract the elastic properties. Based on this prediction and the experimental results, Pharr and Bolshakov's effective indenter profile could be determined. The extracted elastic-viscoelastic parameters using the solution based on Pharr and Bolshakov's effective indenter were independent of the reloading levels.

The effect of the film thickness on the phase transformations encountered in sputtered titanium-nickel (TiNi) shape-memory films due to thermal cycling in the temperature range of −150 to 150 °C was examined in the context of electrical resistivity (ER) measurements. A hysteresis in the ER response was observed for film thickness greater than 300 nm. This phenomenon is characteristic of shape-memory materials and is attributed to the rhombohedral (R) phase produced during cooling from the high-temperature cubic austenite phase to the low-temperature monoclinic martensite phase. The decrease of the TiNi film thickness below 300 nm resulted in a smaller ER hysteresis, leading eventually to its disappearance for film thickness less than ∼50 nm. The results indicate that spatial constraints introduced by the film surface and film/substrate interface generate a resistance force, which prevents lattice distortion and twinning. The inhibition of these mechanisms, which control self-accommodation R-phase transformation, leads to the suppression and eventual disappearance of the shape memory effect for film thickness less than ∼100 nm.