Electron spectroscopy surface studies

The mechanism of C02 reduction to methane at Cu electrodes has been proposed by various groups [72-74], most of which involved the splitting of adsorbed CO followed by the hydrogenation of surface C atoms. When DeWulf et al. used X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy to study the reaction [72], they observed surface-bound carbenes (Cu CH2) as an intermediate in the system. Likewise, others used both in situ infrared (IR) reflection absorption spectroscopy and surface-enhanced Raman spectroscopy to observe the initial product of C02 reduction on Cu [74]. Typically, two different linearly bound CO species were identified and attributed to adsorption on either surface defect sites or terraces. 

The Structure of the Metal-Vacuum Interface The Study of Simple Consecutive Processes in Electrochemical Reactions Surface Analysis by Electron Spectroscopy Surface-Enhanced Raman Scattering (SERS Surface Potential at Liquid Interfaces Surface States on Semiconductors... 

Heiland W and Taglauer E 1975 Low energy ion scattering and Auger electron spectroscopy studies of clean nickel surfaces and adsorbed layers Surf. Sc/. 47 234-43... 

Recently, other authors when studying the activation of hydrogen by nickel and nickel-copper catalysts in the hydrogen-deuterium exchange reaction concentrated for example only on the role of nickel in these alloys (56) or on a correlation between the true nickel concentration in the surface layer of an alloy, as stated by the Auger electron spectroscopy, and the catalytic activity (57). 

The information contained in ESCA (Electron Spectroscopy for Chemical Analysis) spectra [331] makes the method particularly suitable for determinations of surface compositions, chemical bonding of surface atoms and changes which occur at solid surfaces during reaction [312], Applications of this technique to the study of reactions of and between solids are awaited with interest. 

X-ray scattering studies at a renewed pc-Ag/electrolyte interface366,823 provide evidence for assuming that fast relaxation and diffu-sional processes are probable at a renewed Sn + Pb alloy surface. Investigations by secondary-ion mass spectroscopy (SIMS) of the Pb concentration profile in a thin Sn + Pb alloy surface layer show that the concentration penetration depth in the solid phase is on the order of 0.2 pm, which leads to an estimate of a surface diffusion coefficient for Pb atoms in the Sn + Pb alloy surface layer on the order of 10"13 to lCT12 cm2 s i 820 ( p,emicai analysis by electron spectroscopy for chemical analysis (ESCA) and Auger ofjust-renewed Sn + Pb alloy surfaces in a vacuum confirms that enrichment with Pb of the surface layer is probable.810... 

The technique of photoemission electron spectroscopy (PEEM) is a particularly attractive and important one for spatially resolved work function measurements, as both the Kelvin probe technique and UPS are integral methods with very poor ( mm) spatial resolution. The PEEM technique, pioneered in the area of catalysis by Ertl,72-74 Block75 76 and Imbihl,28 has been used successfully to study catalytic oscillatory phenomena on noble metal surfaces.74,75... 

The apparatuses used for the studies of both ammonia synthesis emd hydrodesulfurization were almost identical, consisting of a UHV chamber pumped by both ion and oil diffusion pumps to base pressures of 1 x10 " Torr. Each chamber was equipped with Low Energy Electron Diffraction optics used to determine the orientation of the surfaces and to ascertain that the surfaces were indeed well-ordered. The LEED optics doubled as retarding field analyzers used for Auger Electron Spectroscopy. In addition, each chamber was equipped with a UTI 100C quadrupole mass spectrometer used for analysis of background gases and for Thermal Desorption Spectroscopy studies. 

A relatively new arrangement for the study of the interfacial region is achieved by so-called emersed electrodes. This experimental technique developed by Hansen et al. consists of fully or partially removing the electrode from the solution at a constant electrical potential. This ex situ experiment (Fig. 9), usually called an emersion process, makes possible an analysis of an electrode in an ambient atmosphere or an ultrahigh vacuum (UHV). Research using modem surface analysis such as electron spectroscopy for chemical analysis (ESCA), electroreflectance, as well as surface resistance, electrical current, and in particular Volta potential measurements, have shown that the essential features (e.g., the charge on... 

Kim KS, Winograd N, Davis RE. 1971. Electron spectroscopy of platinum-oxygen surfaces and application to electrochemical studies. J Am Chem Soc 93 6296-6297. 

Conversion electron Mossbauer spectroscopy (CEMS) measurements with back scattering geometry have the merit that spectra can be obtained from a sample with much less isotope content compared with transmission measurements. Another merit is that a sample, deposited on a thick substrate, could be measured, and that because of the limited escape depth of the conversion electrons, depth-selective surface studies are possible. The CEMS technique was found to be best applicable to specimens of 10-100 pg Au cm, i.e., about two orders of magnitudes thinner than required for measurements in transmission mode [443]. This way (1) very thin films of gold alloys, as well as laser- and in beam-modified surfaces in the submicrometers range of depth [443], and (2) metallic gold precipitates in implanted MgO crystals [444] were investigated. 

The effects of tin/palladium ratio, temperatnre, pressnre, and recycling were studied and correlated with catalyst characterization. The catalysts were characterized by chemisorption titrations, in situ X-Ray Diffraction (XRD), and Electron Spectroscopy for Chemical Analysis (ESCA). Chemisorption studies with hydrogen sulfide show lack of adsorption at higher Sn/Pd ratios. Carbon monoxide chemisorption indicates an increase in adsorption with increasing palladium concentration. One form of palladium is transformed to a new phase at 140°C by measurement of in situ variable temperature XRD. ESCA studies of the catalysts show that the presence of tin concentration increases the surface palladium concentration. ESCA data also indicates that recycled catalysts show no palladium sulfide formation at the surface but palladium cyanide is present. 

These surface kinetics studies initially focused on the dissociation of NO. For instance, Comelli and co-workers reported on the kinetics of the isothermal decomposition of NO on Rh(110) at temperatures ranging from 198 to 240 K and NO coverages below 0NO 0.3 ML [45], Auger electron spectroscopy (AES) lineshape analysis was used to measure the amount of undissociated NO as a function of time, and the resulting 0NO(t)... 

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