Unusual stress behaviour of CeO2-doped diamond-like carbon nanofilms

CeO₂-doped diamond-like carbon (DLC) films with thicknesses of 180–200 nm were deposited by unbalanced magnetron sputtering. When the CeO₂ concentration is in the range 5–8%, the residual compressive stress of the deposited films is reduced by 90%, e.g. from about 4.1 GPa to 0.5 GPa, whereas their adhesion strength increases. These effects are attributed to the dissolution of CeO₂ within the DLC amorphous matrix and a widening interface between the DLC film and the Si substrate, respectively.     

A new orthorhombic approximant of the icosahedral Al–Cu–Fe quasicrystal

We report on the formation of a new crystalline approximant phase of the icosahedral (i-)Al–Cu–Fe quasicrystal. This phase is formed during sintering of Al-based composites reinforced with i-AlCuFeB quasicrystalline particles. The structure of this phase has been characterized by transmission electron microscopy (TEM) and high-resolution electron microscopy (HREM). TEM revealed that it is a B-centred orthorhombic phase with lattice parameters a = 1.166 nm, b = 1.195 nm and c = 3.44 nm. Its chemical composition, as determined by electron energy loss spectroscopy (EELS), is close to Al_76.9Cu_2.7Fe_20.4, with an average number of valence electrons per atom e/a of 1.92, similar to the value in all other approximants of the i-phase discovered thus far. Initial results on local atomic arrangements along one of its pseudo-5-fold axes are also presented.     

Relationship between microstrain and lattice parameter change in nanocrystalline materials

A lattice distortion, represented by microstrain and lattice parameter change, is frequently observed in nanocrystalline (NC) materials. In this letter, we develop a quantitative model to account for this phenomenon. The internal stress induced by the excess volume at grain boundaries is suggested to be the main reason for the lattice distortion. NC materials, prepared by the milling and crystallization method, were used for analysis and comparison. Theoretical calculation shows a reasonable agreement with experimental observations in the grain-size range from 5 to 100 nm. Our results indicate that there is an inherent relationship between microstrain and lattice parameter change in NC materials.     

Transmission electron microscopy study of a new silicon nitride phase

An abnormally large phase, which was found in the precursor-derived Si 3.0 B 1.1 C 5.3 N 3.0 ceramics after crystallization under a nitrogen pressure of 100bar at 1800C for 3h, has been characterized by means of transmission electron microscopy and electron-energy-loss spectroscopy (EELS). EELS analysis shows that this phase consists of only silicon and nitrogen, no other elements being detected. The analysis of selected-area diffraction and convergent-beam electron diffraction in conjunction with EELS reveals that the unknown phase is a variant of silicon nitride. It has a hexagonal structure with lattice parameters a =0.737nm and c =0.536nm, and the space group P62c. .     

Hydrogenation of Ti50Zr25Co25 amorphous ribbons and its effect on their structural and mechanical properties

Changes in the structure and mechanical properties of Ti₅₀Zr₂₅Co₂₅ melt-spun ribbons upon electrolytic hydrogenation have been investigated. Structural analyses of the as-spun ribbons revealed the sporadic presence of icosahedral (i) quasicrystalline short-range order (SRO) in the amorphous structure. Upon cathodic charging with hydrogen, the i-SRO vanished for a hydrogen content of about 21 at.% (hydrogen-to-metal atom ratio, H/M: 0.26), resulting in a fully amorphous structure. Simultaneously, the fracture strength was found to increase while the ribbons preserved their bending ductility. However, a significant reduction in the fracture strength and ductility of the ribbons was observed for hydrogen concentrations larger than 26 at.%. Variations in the mechanical stability are discussed based on a structure-property correlation.     

Difference in microstructure of Zr41Ti14Cu12.5Ni10Be22.5 glasses prepared in a 52 m drop tube and by water quenching

A 52 m drop tube has been used to solidify bulk-glass-forming Zr₄₁Ti₁₄Cu_12.5Ni₁₀Be_22.5 alloy. Glassy balls with different sizes solidified from the droplets whose structural features, glass-transition behaviour and crystallization kinetics have been investigated. The results indicate that the apparent activation energies of the glass transition and main crystallization reaction are significantly different from those of samples prepared by water quenching. The structural difference between the two types of glassy specimen is revealed by compression studies and in situ energy-dispersive X-ray diffraction. The results are important for understanding the structural features of bulk-forming glasses.     

Effects of irradiation with electrons of different energies on the dark conductivity and the network of hydrogenated amorphous silicon films

The effects of irradiation with electrons having energies in the range 0.7–1.7 MeV on the dark conductivity and the network of hydrogenated amorphous silicon (a-Si:H) thin films have been studied. The dark conductivity measurements show that electron irradiation leads to a degradation in the dark conductivity, with the degradation being greater at lower electron energies. The Raman results suggest that the irradiation induces structural defects in the a-Si:H films, with the lower energy electrons producing more disorder in the amorphous network.     

Tensile behaviour of submicrocrystalline ferritic steel processed by large-strain deformation

Mechanical tests have been carried out on Fe–15%Cr ferritic stainless steel with various microstructures. Ultrafine-grained microstructures with grain sizes of 0.2–0.3 µm were developed by large-strain cold-working and light annealing. The effects of severe deformation on the mechanical behaviour of as-processed and recovered steel were evaluated with reference to the same material having conventional work-hardened and recrystallised microstructures. Despite the low dislocation density in the fine grain interiors in the as-processed state, the samples with strain-induced submicrocrystalline structure were characterised by high internal stresses that resulted in a higher strength than could be expected from simple grain-size strengthening. These internal stresses were associated with a non-equilibrium state of strain-induced grain boundaries after severe deformation.     

Transmission electron microscopy characterization of the high-Tc superconductor HgBa2Ca3Cu4O 10+ delta

The structures of HgBa3Ca4Cu4O10+ delta(Hg-1234) samples have been characterized by means of high-resolution electron microscopy, electron diffraction, X-ray energy-dispersive spectroscopy (XEDS) and electron-energy-loss spectroscopy (EELS) techniques. A modulated structure with a modulation vector of q = (0.036-0.048) b* + 0.5c* was found for Hg-1234. High-resolution electron microscopy on the modulated structure revealed slight displacements of atomic layers along the c direction. The anomalous contrast induced by the modulation was observed to be distributed asymmetrically between the HgOdelta layers, leading to the breakdown of the (001) mirror symmetry of the basic structure. XEDS compositional analyses showed a depletion of mercury for the modulated Hg1234 compared with the unmodulated Hg-1234, while EELS analysis suggested the presence of carbon in the modulated Hg-1234 phase. In addition, a sidecentred ordered (Cu, Hg)-1223 phase with low mercury content was identified as one of the major impurity phases in the Hg-1234 samples.