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Hydrogenation surface location

The lower activation energy may arise from a smaller binding energy for a hydrogen atom located on the surface of a column, compared to in the bulk. It is known that the surface of the columns contain polymerically bonded hydrogen (Knights and Lujan, 1979), which will have a bonding structure that differs from that found in the bulk of CVD-quality a-Si H. [Pg.430]

In electrode reactions of the type H+/H2, 02/H20, and probably many organic redox systems, the electrode surface may be involved by virtue of the presence of adsorption sites where intermediates in the reaction mechanism, e.g. atomic hydrogen, are located. Generally, the reaction rate is higher at metals with a larger adsorptive capacity. This is a particular form of electrocatalysis, which is a subject of still-growing interest. [Pg.282]

As shown in Figure 6.49a, the cracks grow by slip dissolution due to diffusion of active water molecules, halide ions, etc., to the crack tip, followed by a rupture of the protective oxide film by strain concentration, fretting contact between the crack faces. This is followed by dissolution of the fresh exposed surface and growth of the oxide on the bare surface. For the alternative mechanism of hydrogen embrittlement in aqueous media, the critical steps involve diffusion of water molecules or hydrogen ions to the crack tip reduction to hydrogen atoms at the crack tip surface diffusion of adsorbed atoms to preferential surface locations absorption and diffusion to critical locations in the... [Pg.416]

The presence of a H-bond in the PHg dimer is even less likely. Frisch et al. " found the equilibrium structure to be of cyclic type with no other minima on the surface. The two P atoms are 4.346 A from one another and each of the bridging hydrogens is located 88° from the P- P axis. The electronic contribution to the binding energy is less than 1 kcal/mol. After reductions of this quantity by zero-point vibrational energies and removal of BSSE, it is questionable whether this dimer would be bound at all. [Pg.89]

In the above equilibria by Hs" " we denote the hydrogen ions located near to the surface. According to the first model, the surface oxygens, with an arbitrary... [Pg.16]

Hence, those parts of the surface, where the hydrogen is located, cannot take part in the gasification process as it might if the hydrogen was absent. As a result, the CO removal... [Pg.288]

In direct-flame SOFCs, part of the fuel gas is combusted in an ordinary burner with an open flame. When the combustible fuel-oxygen mixture is fuel-rich, then a partial fuel reforming wiU occur in the flame yielding hydrogen and carbon monoxide CO. The SOFC anode is set up in the immediate vicinity of the flame, within a few millimeters. There these reforming products are oxidized elec-trochemically. The surrounding air has immediate access to the cathode surface, located on the opposite side of the cell. The fuel cell itself is heated to its working temperature by the flame. [Pg.145]


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See also in sourсe #XX -- [ Pg.259 , Pg.260 , Pg.261 ]




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