Dissociative Chemisorption of

Above room temperature the exposure of Fe to N2 leads to the formation of N through dissociative chemisorption, 2(8) + 2 = 2N. A number of reviews of 

---

NakatsujI H and Nakal H 1990 Theoretical study on molecular and dissociative chemisorptions of an O2 molecule on an Ag surface dipped adcluster model combined with symmetry-adapted cluster-configuration interaction method Chem. Phys. Lett. 174 283-6... 

H] Asscher M, Haase G and Kosloff R 1990 Tunneling mechanism for the dissociative chemisorption of Nj on metal surfaces Vacuum 41 269... 

Kroes G J, Wiesenekker G, Baerends E J, Mowrey R C and Neuhauser D 1996 Dissociative chemisorption of H2 on Cu(IOO)—a four-dimensional study of the effect of parallel translational motion on the reaction dynamics J. Chem. Phys. 105 5979... 

Alford J M, Weiss F D, Laaksonen R T and Smalley R E 1986 Dissociative chemisorption of H2 on niobium cluster ions. A supersonic cluster beam FT-ICR experiment J. Rhys. Chem. 90 4480... 

Jensen J A, Yan C and Kummel A C 1995 Energy dependence of abstractive versus dissociative chemisorption of fluorine molecules on the silicon (111)-(7 7) surface Science 267 493-6... 

Fischer-Tropsch ohgomerization of CO -1- H9 to make hydrocarbons and oxygenated compounds was originally catalyzed by cobalt, which forms the active carbonyl, but now iron promoted by potassium is favored. Dissociative chemisorption of CO has been observed in this process. 

In the foregoing it has been discus.sed how a metal can dissociate H2. Fig. 3.6 explains the principle of catalysis with an example of the hydrogenation of ethylene, for which dissociative chemisorption of hydrogen is an elementary step in the catalytic cycle. The adsorption of alkenes, on the other hand, is non-dissociative. 

Shin J, Tomquist WJ, Korzeniewski C, Hoaglund CS. 1996. Elementary steps in the oxidation and dissociative chemisorption of ethanol on smooth and stepped surface planes of platinum electrodes. Surf Sci 364 122. 

Of crucial significance in deciding between various models have been estimates of the number of copper atoms required to transform the surface into a (2 x 3)N phase. This was the approach adopted by Takehiro et al 2 in their study of NO dissociation at Cu(110). They concluded that by determining the stoichiometry of the (2 x 3)N phase that there is good evidence for a pseudo-(100) model, where a Cu(ll0) row penetrates into the surface layer per three [ll0]Cu surface rows. It is the formation of the five-coordinated N atoms that drives the reconstruction. The authors are of the view that their observations are inconsistent with the added-row model. The structure of the (2 x 3)N phase produced by implantation of nitrogen atoms appears to be identical with that formed by the dissociative chemisorption of nitric oxide. 

The classical and traditional view is that for dissociative chemisorption of diatomic molecules to occur at metal surfaces, it is essential that two adjacent (vacant) sites are available ... 

This model has, however, never been established experimentally and one can envisage that, as was suggested for the dissociative chemisorption of dioxygen, the process could involve just one surface site with the exothermicity associated... 

Oudar and co-workers studied the dissociative chemisorption of hydrogen sulfide at Cu(110) surfaces between 1968 and 1971.3,14 As in the case of Ni(110) described below, a series of structures were identified, which in order of increasing sulfur coverage were described as c(2 x 2), p(5 x 2) and p(3 x 2). In contrast to nickel, the formation of the latter phase is kinetically very slow from the decomposition of H2S and could only be produced at high temperatures and pressures. The c(2 x 2) and p(5 x 2) structures were confirmed by LEED,15 17 but the p(3 x 2) phase has not been observed by H2S adsorption since Oudar and colleagues work. 

Transfer hydrogenolysis of benzyl acetate was studied on Pd/C at room temperature using different formate salts.244 Hydrogen-donating abilities were found to depend on the counterion K+ > NH4 + > Na+ > Li+ > H+. Formate ion is the active species in this reaction. Adsorption of the formate ion on the Pd metal surface leads to dissociative chemisorption resulting in the formation of PdH- and C02. The kinetic isotope effect proves that the dissociative chemisorption of formate is the rate-limiting step. The adsorption and the surface reaction of benzyl acetate occurs very rapidly. 

Scheme S. Hydrogen exchange in benzene by an abstraction-addition mechanism involving dissociative chemisorption of the reactant [Farkas and Farkas (32)].

The conclusions from this work were (i) that the mechanism that operates is of wide applicability, (ii) that exchange proceeds by either the dissociative chemisorption of benzene or by the dissociation of benzene which has previously been associatively chemisorbed, and (iii) that M values of about 2 indicate that further dissociation of surface-area measurements. Surface areas of metal films determined by the chemisorption of hydrogen, oxygen, carbon monoxide, or by physical adsorption of krypton or of xenon concur... 

In our third example (52), dissociative chemisorption of Li2, B2, C2, 02, N2, F2, CO, NO and ethylene on (100)W and Ni surfaces was examined. The metal surfaces are represented by means of nine-atom clusters, arranged as in Fig. 35. Experimental geometry was used for the adsorbates. The standard EHT method was used, i.e. with charge-independent atomic ionization potentials. Charge transfer between adsorbate and surface was explored... 

From thermodynamic considerations it is evident that bulk nickel cannot be oxidized by CO2. However, it is not justified to conclude from this that dissociative chemisorption of CO2 will not occur. Consider, for example, the chemisorption of oxygen or hydrogen which on several metals takes place under conditions where bulk oxides or hydrides are not at all thermodynamically stable. Dissociative adsorption of CO2 has indeed been observed by Eischens and Pliskin (35). 

The low-frequency band in the spectrum of sample Af was superposed on a rather intense high background absorption band its exact shape could not be determined. The conclusion that these bands are due to the presence of CO at the surface follows from their close similarity to those found upon adsorption of CO on the same samples. Hence, dissociative chemisorption of C02 does indeed take place. However, the CO bands observed upon dissociative adsorption of C02 are much weaker than those produced by CO directly adsorbed as such. This becomes evident if we compare them with the nitrogen absorption bands in Figs. 8 and 9 where... 

Whereas determination of chemisorption isotherms, e.g., of hydrogen on metals, is a means for calculating the size of the metallic surface area, our results clearly demonstrate that IR studies on the adsorption of nitrogen and carbon monoxide can give valuable information about the structure of the metal surface. The adsorption of nitrogen enables us to determine the number of B5 sites per unit of metal surface area, not only on nickel, but also on palladium, platinum, and iridium. Once the number of B5 sites is known, it is possible to look for other phenomena that require the presence of these sites. One has already been found, viz, the dissociative chemisorption of carbon dioxide on nickel. 

---