The fatigue crack growth kinetics and tensile deformation of bulk nanocrystalline Al-7.5Mg were investigated. Nanocrystalline particulates were first prepared by mechanically ball milling spray atomized Al-7.5Mg powders in liquid nitrogen. These particulates were then degassed, consolidated by hot isostatic pressing, and extruded into rods. Bulk nanocrystalline Al-7.5Mg has significantly higher fatigue crack growth rates and lower fatigue crack growth thresholds than those of ingot-processed 7050-T7451. The fatigue crack growth thresholds exhibit only a weak stress ratio dependency and can be identified as having a Class I behavior when using the fatigue classification proposed by Vasudevan and Sadananda. In 3.5% NaCl solution, fatigue crack growth rates of bulk nanocrystalline Al-7.5Mg are as much as three times higher than those obtained in air. Tensile fracture of bulk nanocrystalline Al-7.5Mg is preceded by the formation of a localized shear band. In contrast to the low dislocation density in the as-extruded material, the gage section and the shear band region both exhibited a high dislocation density and dislocation cell structure.

Local elastic properties and microstructural features of low-density polyethylene-polypropylene (LDPE-PP) blends have been studied by microacoustical technique, differential scanning calorimetry and infrared spectroscopy. Focused ultrasonic beam of acoustic microscope has been employed to measure elastic wave velocities, bulk and shear elastic moduli and Poisson ratio. The experiments show that the mechanical properties of immiscible LDPE-PP blends are non-additivily changeable in relation to ones of primary gomopolymers. Maximum of the moduli values is achieved with small addition of LDPE to PP. Additional drawing of bipolymer shows essential increasing of orientation ability for PP chains in 5/95 – 10/90 % LDPE-PP compositions. DSC curves show no significant deviations in melting temperature and crystallinity degree for different compositions of PP and LDPE phases. Internal microstructure has been imaged for the blends by acoustic microscopy technique. It allows revealing dispersivity of components over the blend body.

Well defined spherical particles of γ- Fe2O3 have been synthesized in the pores of a polymer matrix in the form of beads by an ion exchange and precipitation reaction. The particle size distribution is a gaussian with an average diameter of 80 A. The DC magnetic susceptibility and the magnetization of the nanocomposite has been measured between 4 and 300 K using a Faraday balance and a magnetometer, respectively. The magnetic measurements demonstrate that the particles are superparamagnetic with a blocking temperature Tb about 55 K. The optical absorption edge of the mesoscopic system is red shifted with respect to single crystal films of γ-Fe2O3 with an absorption tail extended deeply in the gap. Although lattice distortion and existence of excitonic states in the gap can explain the absorption behavior, the red shift can successfully be explained by the quantum confinement of an electron-hole pair in a spherical well.

Nanostructured Cu/304 stainless steel (SS) multilayers were prepared by magnetron sputtering at room temperature. 304SS has a face-centered cubic (fcc) structure in bulk. However, in the Cu/304SS multilayers, the SS layers exhibited fcc structure for layer thickness of less than or equal to 5 nm. For 304SS layer thickness larger than 5nm, bcc 304SS grains were observed to grow on top of the initial ≈ 5 nm of fcc SS. The maximum hardness of Cu/304SS multilayers was ≈ 5.5 GPa (factor of two enhancement compared to rule of mixtures hardness) achieved at a layer thickness of 5nm, with a decrease in hardness with decreasing layer thickness below 5 nm. The hardness of fcc/fcc Cu/304SS multilayers (layer thickness ≤ 5 nm) is compared with Cu/Ni, another fcc/fcc system, to gain insight on how the mismatch in physical properties such as lattice parameters and shear moduli of the constituent layers affect the peak hardness achieved in these nanoscale systems.

In this report, we explore the possibilities of the fabrication and characterization of ferroelectric nano-structures by various methods. Techniques include the self-assembly route and direct electron beam lithography. The chemical self-assembly route, which adopted the microemulsionmediated synthesis, appeared to be very encouraging for producing very small monodispersed nano particles and powders, with sizes of 10–60 nm. The possibility to form a two dimensional arrangement of these micro droplets was explored with a suitable choice of the substrate material, and the method of coating. For the patterns prepared by the e-beam technique, a strong coupling between two closely spaced nano elements was observed, the spacing between them was found to be the key factor in tailoring their interaction, i.e., whether they would arrange themselves in rod-like pattern or a two dimensional array of isolated squares or circles.

There is great potential for the use of nanostructures in numerous applications. Investigation of nanoparticle films and structures is an important area of research for the production of nanoengineered devices. However, for these devices to become a reality, a production method that can yield high-rate synthesis of nanostructured powders is necessary. The hypersonic plasma particle deposition (HPPD) process has been shown to be capable of such high-rate production of nanoparticle films and structures. Versatile in its ability to manufacture nanoparticles of different chemistries HPPD also has the capability of in situ particle consolidation and assembly. In this study, chemically diverse films and structures have been produced by HPPD on a variety of substrates. Using novel specimen preparation techniques, these nanoparticles have been characterized by TEM. Fundamental issues of importance have been investigated for both the nanoparticle structure and the constituent nanoparticles. These issues include nanoparticle crystallinity and defect structure. The chemical homogeneity and structural characteristics of the deposition are also investigated. This application of microscopy to aid process development has resulted in insights into the nanoparticle formation process and the dynamics of the HPPD process.

With a view to investigating how a thin film twist-bonded to a host substrate can have compliant behavior from a plasticity point of view, the onset and spread of edge dislocations throughout a mesa are studied. The discussion focuses on the energy relaxed by such dislocations in a mesa made from two coherently bonded lattice-mismatched layers twist-bonded onto a host substrate and patterned down to the film/host substrate interface. Our theoretical results show that the confinement of threading dislocations into a thin twist-bonded film is energetically favorable allowing the overgrowth of a mismatched layer exempt of any threading dislocation at least as far as mesas are concerned.

AFM-scratching was performed through thin oxide layer which was either a native oxide layer (1.5 – 2 nm thick) or a thermal oxide layer (10 nm thick). Due to their insulating properties, the SiO2 films act as masks for the metal electrochemical deposition. In the scratched openings copper deposition can take place selectively and thus nano-scale metal lines could be successfully plated onto the p-type silicon substrates. Using particularly, if sufficiently thick thermal oxide has advantages over the native oxide, it allows a H-termination of the Si within the grooves (HF treatment) without eliminating the oxide layer on the rest of the surface.

We have developed nano-foamed OxD which has good properties such as dielectric constant=2.2, homogeneous distributed nano pores, smooth surface based on polybenzoxazole chemistry and nano-foaming technology. The nano-foamed OxD also has excellent thermal stability, chemical stability and etching property. The developed nano-foamed OxD is one of good candidates for copper damascene structure to achieve shrinking dimensions of future semi-conductor devices.