Low-energy electron diffraction-Auger

The studies of Ertl and associates employed a surface consisting of the (0001) face of a ruthenium single crystal. Copper was deposited on the ruthenium surface by exposing the surface to a flux of copper atoms obtained by evaporation of a copper source. From low energy electron diffraction, Auger electron spectroscopy, thermal desorption, and work function measurements (18) Ertl and associates concluded that copper deposits on the ruthenium surface at 540 K in the form of a two-dimensional overlayer to coverages of 50 to 60%, beyond which there is a transition to a three-dimensional growth phase. 

However, it seems that the use of the combined electrochemical pre-chamber/UHV main chamber device seems to be the best for these treatments. One of the methods consists of applying the same treatment to platinum single crystals for separate experiments. For characterization, low-energy electron diffraction, Auger electron spectroscopy, or XPS was used. Conventional electrochemical experiments were followed with the analysis of the results by taking into account the effect of the unavoidable differences in the required conditions. 

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. 

As mentioned previously, this can be attributed in part to the lack of structure-sensitive techniques that can operate in the presence of a condensed phase. Ultrahigh-vacuum (UHV) surface spectroscopic techniques such as low-energy electron diffraction (LEED), Auger electron spectroscopy (AES), and others have been applied to the study of electrochemical interfaces, and a wealth of information has emerged from these ex situ studies on well-defined electrode surfaces.15"17 However, the fact that these techniques require the use of UHV precludes their use for in situ studies of the electrode/solution interface. In addition, transfer of the electrode from the electrolytic medium into UHV introduces the very serious question of whether the nature of the surface examined ex situ has the same structure as the surface in contact with the electrolyte and under potential control. Furthermore, any information on the solution side of the interface is, of necessity, lost. 

Carbon deposition from CO on a cobalt catalyst at low pressures is known to be a structure-sensitive process. CO is adsorbed molecularly on the low index surfaces (Co (0001)), but its dissociation occurs on the Co (1012), Co (1120), and polycrystalline surfaces.5762 Deposition of carbon on Co (1012) and the probable formation of Co3C have been established by Auger emission spectroscopy (AES) and low-energy electron diffraction (LEED) techniques.66... 

Voltammetry Assisted by Auger Spectroscopy, Electron Energy-Loss Spectroscopy, and Low-Energy Electron Diffraction... 

Polymer films were produced by surface catalysis on clean Ni(100) and Ni(lll) single crystals in a standard UHV vacuum system H2.131. The surfaces were atomically clean as determined from low energy electron diffraction (LEED) and Auger electron spectroscopy (AES). Monomer was adsorbed on the nickel surfaces circa 150 K and reaction was induced by raising the temperature. Surface species were characterized by temperature programmed reaction (TPR), reflection infrared spectroscopy, and AES. Molecular orientations were inferred from the surface dipole selection rule of reflection infrared spectroscopy. The selection rule indicates that only molecular vibrations with a dynamic dipole normal to the surface will be infrared active [14.], thus for aromatic molecules the absence of a C=C stretch or a ring vibration mode indicates the ring must be parallel the surface. 

Low-Energy Electron Diffraction, X-ray Photoelectron Spectroscopy, and Auger Electron Spectroscopy... 

The tools used for the experiments described below have been described in several books and review articles (1-3). Surface structure is determined by low energy electron diffraction (LEED), surface composition by Auger electron spectroscopy (AES), and reaction kinetics and mechanism by temperature programmed reaction spectroscopy (TPRS). Standard ultra-high vacuum technology is used to maintain the surface in a well-defined state. As this article is a consolidation of previously published work, details of the experiments are not discussed here. 

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