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Metallic surface bond

Although the results of these measurements have not been presently completely interpreted in terms of the metal-surface bonding, they indicate the usefulness of the EPR technique m the study of paramagnetic ions adsorbed on the surface of solids. [Pg.99]

Barlow S, Raval R (2003) Complex organic molecules at metal surfaces Bonding, organisation and chirality. Surf Sci Rep 50 201... [Pg.114]

Generally, sorption of metals seems to be more nearly reversible at low than at high pH. This may arise from the fact that the monodentate complexation reaction (4.11) should give way to the bidentate reaction (4.12) at higher pH. The latter reaction, involving two metal-surface bonds, is expected to have a very slow rate in the reverse direction (desorption). Studies of heavy metal bonding on pure oxides have indicated that the adsorption reaction step is fast and probably diffusion controlled kf 10 moles liter sec ), whereas the desorption reaction step has a rate constant that may be as much as three orders of magnitude slower. [Pg.134]

The Quantum Chemistry of Transition Metal Surface Bonding and Reactivity... [Pg.269]

In Chapter 3, we extend the general concepts developed in Chapter 2 on chemisorption and surface reactivity to establish a fundamental set of theoretical descriptions that describe bonding and reactivity on idealized metal substrates in Chapter 3. There is an extensive treatment of the adsorbate transition-metal surface bond, its electronic strnc-ture, bond strength and its influence on its chemical activity. Attention is given to periodic trends in the interaction energy as a function of transition metal and also on the dependence in transition-metal structure. [Pg.9]


See other pages where Metallic surface bond is mentioned: [Pg.178]    [Pg.34]    [Pg.56]    [Pg.1426]    [Pg.43]    [Pg.226]    [Pg.187]    [Pg.126]    [Pg.135]    [Pg.73]    [Pg.77]    [Pg.73]    [Pg.77]    [Pg.9]    [Pg.58]    [Pg.43]    [Pg.702]    [Pg.43]    [Pg.110]   
See also in sourсe #XX -- [ Pg.194 ]




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