Oxidation mechanisms in high pressure dc-sputtered a-Si films

1985 ◽  
Vol 74 (1) ◽  
pp. 11-17 ◽  
Author(s):  
R.R. Koropecki ◽  
R. Arce ◽  
L.S. De Bernardez ◽  
R. Buitrago
1977 ◽  
Vol 16 (8) ◽  
pp. 3660-3664 ◽  
Author(s):  
B. Welber ◽  
M. H. Brodsky

The oxidation mechanisms of a high-silicon mild steel (a fully killed steel) in high pressure (4.1 MPa) CO 2 at 773 K have been investigated with the aid of 18 O as a tracer. In the protective region of oxidation oxide forma­tion occurred at the oxide-gas interface, within the scale and possibly also at the oxide-metal interface. The oxide growth within the scale is believed to occur in a relatively stress-free manner. The results for this steel are compared with those for a low-silicon mild steel, Fe-9% Cr alloys, and nickel.


Author(s):  
Tai D. Nguyen

Polycrystalline silicon (poly-Si) films have found many applications in integrated circuits, and in actuators and sensors. Important considerations in the processing of these devices are structural stability and repeatable mechanical properties of the films. The texture and stress state of the films depend strongly on the microstructures and morphology of the films. Tensile films, which are preferred to compressive films in devices whose lateral dimensions of clamped structures are not to be restricted by compressive buckling, are characterized by equiaxial grain morphology, while compressive films are characterized by columnar grain growth during deposition.A diamond hexagonal (d.h.) Si structure with lattice parameters of a = 3.8Å and c = 6.28Å was first reported in 1963. More recently, transformation from the diamond cubic (d.c.) Si to the hexagonal phase has been observed in Si under hydrostatic pressure at temperatures between 350 C and 700 C, in heavily ion-implanted silicon, and in as-grown, implanted, and annealed CVD Si thin films, in addition to the known high pressure Si phases.


Author(s):  
Marek Malecki ◽  
James Pawley ◽  
Hans Ris

The ultrastructure of cells suspended in physiological fluids or cell culture media can only be studied if the living processes are stopped while the cells remain in suspension. Attachment of living cells to carrier surfaces to facilitate further processing for electron microscopy produces a rapid reorganization of cell structure eradicating most traces of the structures present when the cells were in suspension. The structure of cells in suspension can be immobilized by either chemical fixation or, much faster, by rapid freezing (cryo-immobilization). The fixation speed is particularly important in studies of cell surface reorganization over time. High pressure freezing provides conditions where specimens up to 500μm thick can be frozen in milliseconds without ice crystal damage. This volume is sufficient for cells to remain in suspension until frozen. However, special procedures are needed to assure that the unattached cells are not lost during subsequent processing for LVSEM or HVEM using freeze-substitution or freeze drying. We recently developed such a procedure.


Author(s):  
Robert Corbett ◽  
Delbert E. Philpott ◽  
Sam Black

Observation of subtle or early signs of change in spaceflight induced alterations on living systems require precise methods of sampling. In-flight analysis would be preferable but constraints of time, equipment, personnel and cost dictate the necessity for prolonged storage before retrieval. Because of this, various tissues have been stored in fixatives and combinations of fixatives and observed at various time intervals. High pressure and the effect of buffer alone have also been tried.Of the various tissues embedded, muscle, cartilage and liver, liver has been the most extensively studied because it contains large numbers of organelles common to all tissues (Fig. 1).


Author(s):  
R. W. Ditchfield ◽  
A. G. Cullis

An energy analyzing transmission electron microscope of the Möllenstedt type was used to measure the electron energy loss spectra given by various layer structures to a spatial resolution of 100Å. The technique is an important, method of microanalysis and has been used to identify secondary phases in alloys and impurity particles incorporated into epitaxial Si films.Layers Formed by the Epitaxial Growth of Ge on Si Substrates Following studies of the epitaxial growth of Ge on (111) Si substrates by vacuum evaporation, it was important to investigate the possible mixing of these two elements in the grown layers. These layers consisted of separate growth centres which were often triangular and oriented in the same sense, as shown in Fig. 1.


Author(s):  
E. I. Alessandrini ◽  
M. O. Aboelfotoh

Considerable interest has been generated in solid state reactions between thin films of near noble metals and silicon. These metals deposited on Si form numerous stable chemical compounds at low temperatures and have found applications as Schottky barrier contacts to silicon in VLSI devices. Since the very first phase that nucleates in contact with Si determines the barrier properties, the purpose of our study was to investigate the silicide formation of the near noble metals, Pd and Pt, at very thin thickness of the metal films on amorphous silicon.Films of Pd and Pt in the thickness range of 0.5nm to 20nm were made by room temperature evaporation on 40nm thick amorphous Si films, which were first deposited on 30nm thick amorphous Si3N4 membranes in a window configuration. The deposition rate was 0.1 to 0.5nm/sec and the pressure during deposition was 3 x 10 -7 Torr. The samples were annealed at temperatures in the range from 200° to 650°C in a furnace with helium purified by hot (950°C) Ti particles. Transmission electron microscopy and diffraction techniques were used to evaluate changes in structure and morphology of the phases formed as a function of metal thickness and annealing temperature.


Author(s):  
R.E. Crang ◽  
M. Mueller ◽  
K. Zierold

Obtaining frozen-hydrated sections of plant tissues for electron microscopy and microanalysis has been considered difficult, if not impossible, due primarily to the considerable depth of effective freezing in the tissues which would be required. The greatest depth of vitreous freezing is generally considered to be only 15-20 μm in animal specimens. Plant cells are often much larger in diameter and, if several cells are required to be intact, ice crystal damage can be expected to be so severe as to prevent successful cryoultramicrotomy. The very nature of cell walls, intercellular air spaces, irregular topography, and large vacuoles often make it impractical to use immersion, metal-mirror, or jet freezing techniques for botanical material.However, it has been proposed that high-pressure freezing (HPF) may offer an alternative to the more conventional freezing techniques, inasmuch as non-cryoprotected specimens may be frozen in a vitreous, or near-vitreous state, to a radial depth of at least 0.5 mm.


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