Species surface

One of the most disputed steps is the activation of CO on the catalyst surface. Adsorbed CO may be dissociated according to Equation (14) 

The facile dissociative adsorption of CO on transition metals at low temperatures has been demonstrated by XPS or pulse techniques for Ti, V, Cr and Mn (96] and at elevated temperatures for Ni, Co and Ku with Fc as the borderline case [96, 97J. A more detailed study by Somorjai for Pt (111) surfaces showed that dissociation occurs at the step sites only, and once these are filled, carbon monoxide is absorbed moiccularly [98]. All of the XPS studies on chemisorption on iron, except at very low temperatures, are indicative of dissociative surpikm being the first step in Fischer-Tropsdi reactions (99 101). However, photoelectron spectroscopy has so far not delineated a logical sequence of precursors and intermediates 1102.  

Infrared mcasurcnienls of CO adsorption on nickel surfaces by Martin er qL gave some further insight on the formation mechanism of surface carbide. 

Boudouard reaction of CO. Araki and Ponec were able to show in an elegant experiment, that upon exposure of the C-carbidcd surface with CO/Hj almost exclusively CHa is formed at the initial stage (108). Similar experiments were carried out by Biloen and Sachller on supported Co, Ni and Ru catalysts. Besides the formation of they could detect the formation 

From this the authors concluded that oxygen-free species CH (x 0 to 3) are likely inteimcdiales in methanation. These species were also capable of being incorporated into growing hydrocarbon chains (109 III.  

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The second set of equations is obtained from the first set by the Gibbs integration at constant intensive variables, as was done in obtaining Eq. III-77. It is convenient, in dealing with a surface species, to introduce some special definitions, two of which are... 

As with the other surface reactions discussed above, the steps m a catalytic reaction (neglecting diffiision) are as follows the adsorption of reactant molecules or atoms to fomi bound surface species, the reaction of these surface species with gas phase species or other surface species and subsequent product desorption. The global reaction rate is governed by the slowest of these elementary steps, called the rate-detemiming or rate-limiting step. In many cases, it has been found that either the adsorption or desorption steps are rate detemiining. It is not surprising, then, that the surface stmcture of the catalyst, which is a variable that can influence adsorption and desorption rates, can sometimes affect the overall conversion and selectivity. 

On metals in particular, the dependence of the radiation absorption by surface species on the orientation of the electrical vector can be fiilly exploited by using one of the several polarization techniques developed over the past few decades [27, 28, 29 and 30], The idea behind all those approaches is to acquire the p-to-s polarized light intensity ratio during each single IR interferometer scan since the adsorbate only absorbs the p-polarized component, that spectral ratio provides absorbance infonnation for the surface species exclusively. Polarization-modulation mediods provide the added advantage of being able to discriminate between the signals due to adsorbates and those from gas or liquid molecules. Thanks to this, RAIRS data on species chemisorbed on metals have been successfidly acquired in situ under catalytic conditions [31], and even in electrochemical cells [32]. 

Adsorptive stripping analysis involves pre-concentration of the analyte, or a derivative of it, by adsorption onto the working electrode, followed by voltanmietric iiieasurement of the surface species. Many species with surface-active properties are measurable at Hg electrodes down to nanoniolar levels and below, with detection limits comparable to those for trace metal detemiination with ASV. 

Surface species during the reaction were detected by Fourier transfonn infrared spectroscopy, using the Si-Cl... 

Transmission Fourier Transform Infrared Spectroscopy. The most straightforward method for the acquisition of in spectra of surface layers is standard transmission spectroscopy (35,36). This approach can only be used for samples which are partially in transparent or which can be diluted with an in transparent medium such as KBr and pressed into a transmissive pellet. The extent to which the in spectral region (typically ca 600 4000 cm ) is available for study depends on the in absorption characteristics of the soHd support material. Transmission ftir spectroscopy is most often used to study surface species on metal oxides. These soHds leave reasonably large spectral windows within which the spectral behavior of the surface species can be viewed. 

Fig. 7. Bombardment processes at the surface and in the near-surface region of a sputtering target, where represents the energetic particle used for bombarding the surface <), an adsorbed surface species 0> atoms and x, lattice defects.

These siUca-supported catalysts demonstrate the close connections between catalysis in solutions and catalysis on surfaces, but they are not industrial catalysts. However, siUca is used as a support for chromium complexes, formed either from chromocene or chromium salts, that are industrial catalysts for polymerization of a-olefins (64,65). Supported chromium complex catalysts are used on an enormous scale in the manufacture of linear polyethylene in the Unipol and Phillips processes (see Olefin polymers). The exact stmctures of the surface species are still not known, but it is evident that there is a close analogy linking soluble and supported metal complex catalysts for olefin polymerization. 

The catalysts are prepared by impregnating the support with aqueous salts of molybdenum and the promoter. In acidic solutions, molybdate ions are present largely in the form of heptamers, [Mo2024] , and the resulting surface species are beHeved to be present in islands, perhaps containing only seven Mo ions (100). Before use, the catalyst is treated with H2 and some sulfur-containing compounds, and the surface oxides are converted into the sulfides that are the catalyticaHy active species. 

Proceedings of the 7th International Symposium, Cancun, Mexico, October 5-8,1997 edited by C.H. Bartholomew and G.A. Fuentes Volume 112 Spillover and Migration of Surface Species on Catalysts. 

Comparison of the vibrational frequencies (cm ) of the ethylidyne surface species formed on Rh (111) with those of the ethyiidyne duster compound. 

Vibrational Spectroscopy of Molecules on Surfaces. 0- T. Yates, Jr. and T. E. Madey, eds.) Plenum, New York, 1987. Basic concepts and experimental methods used to measure vibrational spectra of surface species. Of particular interest is Chapter 6 by N. Avery on HREELS. 

Large Specific Surface Area Porous materials can have a large proportion of surface atoms - their surface area within a typical sampling volume of 10 pm can reach 10 pm, which is approximately 10 larger than for a smooth surface crossing the same volume. These effects lead to clearly increased Raman intensities of surface species and also to improved intensity ratios of surface and bulk Raman bands. 

A powerful characteristic of RAIR spectroscopy is that the technique can be used to determine the orientation of surface species. The reason for this is as follows. When parallel polarized infrared radiation is specularly reflected off of a substrate at a large angle of incidence, the incident and reflected waves combine to form a standing wave that has its electric field vector (E) perpendicular to the substrate surface. Since the intensity of an infrared absorption band is proportional to / ( M), where M is the transition moment , it can be seen that the intensity of a band is maximum when E and M are parallel (i.e., both perpendicular to the surface). / is a minimum when M is parallel to the surface (as stated above, E is always perpendicular to the surface in RAIR spectroscopy). 

If it is required that the surface of the sample remains undisturbed during analysis, SIMS must be carried out at very low surface removal rates, typically about 10 monolayer/s. The terms static and dynamic are used to divide the sputtering rate of the sample into regimes where only surface species are observed (static SIMS) or where surface and bulk species are observed (dynamic SIMS). The static limit is usually considered to be <10 ions/cm impinging on the sample surface. Under these conditions, only about 1/1000 atoms on the surface of the sample are struck by a primary ion. 

Cs NMR results for Cs on the surfaces of illite, kaolinite, boehmite and silica gel (Figure 3) show that for this large, low charge cation the surface behavior is quite similar to the interlayer behavior. They also illustrate the capabilities of NMR methods to probe surface species and the effects of RH on the structural environments and dynamical behavior of the Cs. The samples were prepared by immersing 0.5 gm of powdered solid in 50 ml of O.IM CsCl solution at 2 5°C for 5 days. Final pHs were between 4.60 and 7.77, greater than the zero point of charge, except for boehmite, which has a ZPC... 

The effect of Oj, SOj, NOj, HjS, CI2, CO and NH3 on Sn/50%Pb in atmospheres of different relative humidity were investigated but only SO2 and NO2 were active at low concentrations (<100 ppm). An XPS study of Sn/50 7oPb solder exposed to O2, HjO and NO2 was conducted to establish both the surface species formed and the ratio of the concentration of each metal in the surface. Previous XPS studies had only considered the interaction of tin/lead solder with the air . 

While the initial surface species formed on lithium in alkyl carbonates consist of ROC02Li compounds, these species react with water to form Li,CO, C02, and ROH. This reaction gradually changes the composition of the surface films formed on... 

Carbon dioxide has been proposed as an additive to improve the performance of lithium batteries [60]. Aurbach et al. [61] studied the film formed on lithium in electrolytes saturated with C02, and using in situ FTIR found that Li2C03 is a major surface species. This means that the formation of a stable Li2C03 film on the lithium surface may improve cyclability [62], Osaka and co-workers [63] also studied the dependence of the lithium efficiency on the plating substrate in LiC104-PC. The addition of C02 resulted in an increase in the efficiency when the substrate was Ni or Ti, but no effect was observed with Ag or Cu substrates. 

The physicochemical properties of carbon are highly dependent on its surface structure and chemical composition [66—68], The type and content of surface species, particle shape and size, pore-size distribution, BET surface area and pore-opening are of critical importance in the use of carbons as anode material. These properties have a major influence on (9IR, reversible capacity <2R, and the rate capability and safety of the battery. The surface chemical composition depends on the raw materials (carbon precursors), the production process, and the history of the carbon. Surface groups containing H, O, S, N, P, halogens, and other elements have been identified on carbon blacks [66, 67]. There is also ash on the surface of carbon and this typically contains Ca, Si, Fe, Al, and V. Ash and acidic oxides enhance the adsorption of the more polar compounds and electrolytes [66]. 

Lithium carbonate and hydrocarbon were identified in XPS spectra of graphite electrodes after the first cycle in LiPF6/EC-DMC electrolyte [104]. Electrochemical QCMB experiments in LiAsF6/EC-DEC solution [99] clearly indicated the formation of a surface film at about 1.5 V vs. (Li/Li+). However the values of mass accumulation per mole of electrons transferred (m.p.e), calculated for the surface species, were smaller than those of the expected surface compounds (mainly (CF OCC Li ). This was attributed to the low stability of the SEI and its partial dissolution. 

It is appropriate to emphasize again that mechanisms formulated on the basis of kinetic observations should, whenever possible, be supported by independent evidence, including, for example, (where appropriate) X-ray diffraction data (to recognize phases present and any topotactic relationships [1257]), reactivity studies of any possible (or postulated) intermediates, conductivity measurements (to determine the nature and mobilities of surface species and defects which may participate in reaction), influence on reaction rate of gaseous additives including products which may be adsorbed on active surfaces, microscopic examination (directions of interface advance, particle cracking, etc.), surface area determinations and any other relevant measurements. 

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