Numerical Simulation of Surface Diffusion Controlled Motion and Shape Change of Electromigration Voids

1996 ◽  
Vol 428 ◽  
Author(s):  
O. Kraft ◽  
U. E. Mockl ◽  
E. Arzt

AbstractIn order to simulate void motion and shape change of electromigration voids a numerical model was developed in which electromigration-driven diffusion on the void surfaces is assumed to act as the primary transport mechanism. The simulation describes the motion and shape evolution of a "two-dimensional void" having a simple initial shape in an isotropic medium. The current density distribution in the vicinity of a void was calculated by the application of a finite element method. Subsequently, the void shape changes by surface diffusion were examined using a finite difference scheme which includes the influence of gradients in curvature along the void surface. The model has been extended to allow other diffusion pathways, such as grain boundaries. The often observed faceting of voids and the formation of slit-like voids are discussed on the basis of simulations in which anisotropic surface tension and anisotropic surface diffusivity were assumed.

1991 ◽  
Vol 238 ◽  
Author(s):  
J. W. Bullard ◽  
A. M. Glaeser ◽  
Alan W. Searcy

ABSTRACTChannels with widths in the range from 5 μm to 25 μm were formed in {100} surfaces of LiF single crystals by a photolithographic technique. Specimens annealed at or above 0.90 Tm, where Tm is the melting point, and then quenched showed die channels and the ridges between them develop rounded profiles. Evolution of these profiles was evaluated for the various channel widths and for interchannel ridge spacings of 5 to 100 μm in terms of: a) an accepted theoretical model for a surface diffusion controlled process, and b) a model which assumes that shape changes depend only on the relative energies of attachment of atoms in surface sites with various surface curvatures. Either model is consistent with the experimental observations to within the reproducibility in measurements.


2021 ◽  
Vol 26 (2) ◽  
pp. 43
Author(s):  
Constantino Grau Grau Turuelo ◽  
Cornelia Breitkopf

The prediction and control of the transformation of void structures with high-temperature processing is a critical area in many engineering applications. In this work, focused on the void shape evolution of silicon, a novel algebraic model for the calculation of final equilibrium structures from initial void cylindrical trenches, driven by surface diffusion, is introduced. This algebraic model provides a simple and fast way to calculate expressions to predict the final geometrical characteristics, based on linear perturbation analysis. The obtained results are similar to most compared literature data, especially, to those in which a final transformation is reached. Additionally, the model can be applied in any materials affected by the surface diffusion. With such a model, the calculation of void structure design points is greatly simplified not only in the semiconductors field but in other engineering fields where surface diffusion phenomenon is studied.


Development ◽  
1994 ◽  
Vol 120 (4) ◽  
pp. 853-859 ◽  
Author(s):  
M. Leptin ◽  
S. Roth

The mesoderm in Drosophila invaginates by a series of characteristic cell shape changes. Mosaics of wild-type cells in an environment of mutant cells incapable of making mesodermal invaginations show that this morphogenetic behaviour does not require interactions between large numbers of cells but that small patches of cells can invaginate independent of their neighbours' behaviour. While the initiation of cell shape change is locally autonomous, the shapes the cells assume are partly determined by the individual cell's environment. Cytoplasmic transplantation experiments show that areas of cells expressing mesodermal genes ectopically at any position in the egg form an invagination. We propose that ventral furrow formation is the consequence of all prospective mesodermal cells independently following their developmental program. Gene expression at the border of the mesoderm is induced by the apposition of mesodermal and non-mesodermal cells.


2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Wei Kong ◽  
Bo Liu ◽  
Bo Ye ◽  
Zhongping Yu ◽  
Hua Wang ◽  
...  

Titanium dioxide (TiO2) nanocrystals of different shape were successfully synthesized in a new microemulsion system through a solvothermal process. The TiO2nanocrystals were prepared from the reaction of tetrabutyl titanate (TBT),H2O, and oleic acid (OA), which were used as solvent and surfactant at 300∘Cand 240∘Cin a stainless steel autoclave. The sphere, polygon, and rhombus-shaped nanocrystals have been prepared at 300∘Cand the dot- and- rod shaped nanocrystals have been synthesized at 240∘C. The effect of the reaction time on the shape and size of TiO2nanocrystals in this method was studied in the present paper. The size distribution of TiO2nanocrystals prepared at 300∘Cfor different hours is also studied. In addition, an attempt to describe the mechanism of shape change of TiO2nanocrystals was presented in this paper.


1999 ◽  
Vol 73 (2) ◽  
pp. 355-371 ◽  
Author(s):  
Mark Webster ◽  
Nigel C. Hughes

Morphometric analyses of silicified and nonsilicified (preserved in shale) specimens of the olenelloid trilobites Olenellus (Olenellus) gilberti Meek (in White, 1874) and Nephrolenellus geniculatus Palmer, 1998, from the Lower Cambrian C-Shale Member of the Pioche Formation show that even well-preserved specimens in shales have undergone significant changes in lateral as well as vertical dimensions as a result of compaction. Analyses of cephalic landmarks show that in both species compaction causes posteriordirected collapse of the anterior lobe of the glabella, adaxial deformation of the ocular lobes, and abaxial and anterior splaying of genal regions. These shape changes are explicable in terms of observed exoskeletal fracture patterns. Landmarks show an increase in scatter around their ontogenetic trajectories that is generally proportional to the degree of lateral shift each landmark has undergone. Interspecific differences in compactional response may depend on the relative convexity of the cephalon. Olenellus (Olenellus) gilberti is a low-convexity species and shows marked lateral shape change, particularly in the genal region. Nephrolenellus geniculatus is more convex and shows less severe lateral shape change. Landmarks of both species exhibit an average trebling of the degree of scatter around their average ontogenetic trajectories in compacted samples. Because even well-preserved specimens in shales differ in shape from their precompactional appearance, results of morphometric studies utilizing metric distances between landmarks in trilobites where compaction can be detected must be interpreted with caution.


Development ◽  
1995 ◽  
Vol 121 (3) ◽  
pp. 903-914 ◽  
Author(s):  
N. Harden ◽  
H.Y. Loh ◽  
W. Chia ◽  
L. Lim

The Rho subfamily of Ras-related small GTP-binding proteins is involved in regulation of the cytoskeleton. The cytoskeletal changes induced by two members of this subfamily, Rho and Rac, in response to growth factor stimulation, have dramatic effects on cell morphology. We are interested in using Drosophila as a system for studying how such effects participate in development. We have identified two Drosophila genes, DRacA and DRacB, encoding proteins with homology to mammalian Rac1 and Rac2. We have made transgenic flies bearing dominant inhibitory (N17DRacA), and wild-type versions of the DRacA cDNA under control of an Hsp70 promoter. Expression of the N17DRacA transgene during embryonic development causes a high frequency of defects in dorsal closure which are due to disruption of cell shape changes in the lateral epidermis. Embryonic expression of N17DRacA also affects germband retraction and head involution. The epidermal cell shape defects caused by expression of N17DRacA are accompanied by disruption of a localized accumulation of actin and myosin thought to be driving epidermal cell shape change. Thus the Rho subfamily may be generating localized changes in the cytoskeleton during Drosophila development in a similar fashion to that seen in mammalian and yeast cells. The Rho subfamily is likely to be participating in a wide range of developmental processes in Drosophila through its regulation of the cytoskeleton.


1989 ◽  
Vol 92 (3) ◽  
pp. 473-485
Author(s):  
I. Kuter ◽  
B. Johnson-Wint ◽  
N. Beaupre ◽  
J. Gross

We have investigated the relationship between collagenase production, cell shape and stimulatory factors in cell culture. In a homogeneous culture of primary rabbit corneal stromal cells, shape change induced by a variety of agents was not effective in stimulating collagenase secretion. Only in the presence of a biologically active cytokine or phorbol myristate acetate was a correlation seen between changes in cell shape (induced by a second agent) and collagenase secretion by these primary cells. Cell shape changes were not, however, necessary for collagenase secretion, since certain concentrations of endotoxin or lactalbumin hydrolysate effected secretion of the enzyme in the absence of morphological changes. With passaged cells or mixed cell cultures, where cell shape change did correlate with collagenase secretion without the addition of an exogenous agent, the production of an effective cytokine (autocrine or paracrine) was demonstrated. Thus cell shape change seems to be neither universally necessary nor sufficient for the stimulation of collagenase secretion. It is proposed that the function of cytokines may be more immediately related to gene expression in this system than is change in the shape of the cell. The hypothesis is presented that cell shape changes may render the target cells receptive to cytokines, perhaps by replacing the need for a natural cytokine cofactor. It is also demonstrated here that the use of passaged cells, mixed cell cultures containing endogenous cytokine-secreting cells or tissue culture additives can profoundly affect the interpretation of the effect of various agents on collagenase secretion, and may lead to observations that are not directly relevant to cell function in vivo.


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