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Oxidation topographical features

AZ-1350 photoresist was used as a thick bottom layer polymer. AZ resist, thicker than 1.0 was spin-coated on silicon wafer (oxide coated) or substrate with topographic features. The resist was hard-baked for 1 hour at 200 C. SNR film was then spin-coated on a hard-baked AZ resist layer from 5 wt% solution in methylisobutylketone. [Pg.313]

A search for extrema in — V2p reveals maxima in the VSCCs that can be ascribed to bonded and nonbonded electron pairs. The different and distinctive properties of sulfides and oxides are examined in terms of the number and the positions of the electron pairs and the topographic features of the Laplacian maps. The evidence provided by p and its topological properties indicates that the bonded interactions in sulfides are more directional, for a given M-cation, than in oxides. The value and the length of a given M-S bond are reliable measures of a bonded interaction the greater the accumulation of p and the shorter the bond, the greater its shared (covalent) interaction. [Pg.178]

Applications of EPMA include elemental analysis of surfaces and of micron-sized features at a surface. The sensitivity of the method is about 0.2 atom%. It provides a rapid, accurate method for compositional analysis of microscopic features. Elemental mapping of the elements present at the surface can also be done, and the composition correlated to topographical maps obtained from an analytical microscopy method, allowing correlation of topographical features of a surface with elemental composition. Like XRF, EPMA is strictly an elemental analysis technique no information on chemical spe-ciation or oxidation state is obtained. AU elements from boron to uranium can be determined. Given that X-rays can escape from depths of 1000 A or so, EPMA has the deepest definition of surface of the techniques discussed in this chapter. In fact, like XRF, it can be considered to be a bulk analysis technique assuming the sample is homogeneous. [Pg.915]

The changes in topographical features, induced by catalytic gasification, are quite different from those changes induced in pure carbons. These changes are best described by examination of scanning electron micrographs of surfaces of oxidized carbons. [Pg.273]

Topographical features, before and after oxidation with carbon dioxide, are as seen in Figures 5.28 and 5.29. When nickel is present in the PFA carbon (Ni C = 1 4500 atomic ratio) then oxidation with carbon dioxide at 873 K produced extensive isolated (non-uniform) pits (20 xm in diameter) as illustrated in Figure 5.28. When copper is present in the PFA carbon (Cu C = 1 4500 atomic ratio) then oxidation with carbon dioxide at 893 K to 9 wt% bum-off produced selective (non-uniform) pitting as illustrated in Figure 5.29. [Pg.273]

Holes are next cut all the way through the first oxide layer (ANCHORl) to anchor structures defined in Polyl to the substrate after the PSG sacrificial spacer layer has been etched. An example is shown in Figure 1.8 [7]. Note that the polysilicon is a conformal coating, so that topographic features, such as the anchor holes, are replicated in the layers deposited on top of them. This replication of topography can give rise to mechanical interferences for features defined in the overlayers. [Pg.9]


See other pages where Oxidation topographical features is mentioned: [Pg.132]    [Pg.25]    [Pg.383]    [Pg.146]    [Pg.132]    [Pg.89]    [Pg.211]    [Pg.132]    [Pg.19]    [Pg.344]    [Pg.328]    [Pg.1039]    [Pg.55]    [Pg.221]    [Pg.268]    [Pg.202]    [Pg.494]    [Pg.24]    [Pg.437]    [Pg.121]    [Pg.80]    [Pg.81]    [Pg.175]    [Pg.78]    [Pg.40]    [Pg.89]    [Pg.249]    [Pg.348]    [Pg.245]   
See also in sourсe #XX -- [ Pg.273 ]




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Oxidation features

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