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Subsurface hydrogen

The major role of TOF-SARS and SARIS is as surface structure analysis teclmiques which are capable of probing the positions of all elements with an accuracy of <0.1 A. They are sensitive to short-range order, i.e. individual interatomic spacings that are <10 A. They provide a direct measure of the interatomic distances in the first and subsurface layers and a measure of surface periodicity in real space. One of its most important applications is the direct determination of hydrogen adsorption sites by recoiling spectrometry [12, 4T ]. Most other surface structure teclmiques do not detect hydrogen, with the possible exception of He atom scattering and vibrational spectroscopy. [Pg.1823]

Olsen R A, Philipsen P H T, Baerends E J, Kroes G J and Louvik O M 1997 Direct subsurface adsorption of hydrogen on Pd(111) quantum mechanical calculations on a new two-dimensional potential energy surfaced. Chem. Phys. 106 9286... [Pg.2236]

Etch Mechanisms. Most wet etches for the compound semiconductors employ oxidation of the semiconductor followed by dissolution of the oxide. For this reason, many wet etches contain the oxidant hydrogen peroxide, although nitric acid can also be used. One advantage of wet etching over dry is the absence of subsurface damage that is common with dry etching. Metal contacts placed on wet-etched surfaces exhibit more ideal characteristics than dry-etched surfaces. [Pg.381]

Greeley J, Mavrikakis M. 2005. Surface and subsurface hydrogen adsorption properties on transition metals and near-surface alloys. J Phys Chem B 109 3460-3471. [Pg.88]

Groundwater extraction Ex situ hydrogen peroxide, or permanganate into die subsurface to oxidize contaminants Extraction of contaminated... [Pg.1003]

FIGURE 2.27 Two possible mechanisms to explain deuterium distributions resulting from deuteriumation and exchange of methyl vinyl ketone. Deuterium is assumed to move subsurface and to attack adsorbed carbons from threefold hollows. Path A multiple exchange by repeated addition-rotation-abstraction at the [3-carbon (classic mechanism) path B I -A hydrogen shift followed by desorption as enol. [Pg.68]

Hydrogen atoms are on the surface and compete with the substrate for active sites however, emerging evidence suggests that both surface and subsurface hydrogens are involved in reactions. [Pg.293]


See other pages where Subsurface hydrogen is mentioned: [Pg.24]    [Pg.24]    [Pg.344]    [Pg.485]    [Pg.937]    [Pg.24]    [Pg.24]    [Pg.344]    [Pg.485]    [Pg.937]    [Pg.717]    [Pg.161]    [Pg.455]    [Pg.257]    [Pg.257]    [Pg.257]    [Pg.257]    [Pg.1230]    [Pg.75]    [Pg.102]    [Pg.170]    [Pg.530]    [Pg.115]    [Pg.127]    [Pg.129]    [Pg.130]    [Pg.131]    [Pg.131]    [Pg.136]    [Pg.137]    [Pg.138]    [Pg.141]    [Pg.576]    [Pg.580]    [Pg.717]    [Pg.40]    [Pg.48]    [Pg.85]    [Pg.292]    [Pg.293]   
See also in sourсe #XX -- [ Pg.24 , Pg.48 ]

See also in sourсe #XX -- [ Pg.24 , Pg.48 ]




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Hydrogenation from subsurface hydrogen

Subsurface

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