Ultrahigh vacuum surface analysis

Campbell R A and Goodman D W 1992 A new design for a multitechnique ultrahigh vacuum surface analysis chamber with high-pressure capabilities Rev. Sc/. Instrum. 63 172... 

UHV surface analysis, apparatus designs, 36 4-14 see also Ultrahigh vacuum surface analysis mechanisms, 32 313, 319-320 Modified Raney nickel catalyst defined, 32 215-217 hydrogenation, 32 224-229 Modifying technique of catalysts, 32 262-264 Modulated-beam mass spectrometry, in detection of surface-generated gas-phase radicals, 35 148-149 MojFe S CpjfCOlj, 38 352 Molar integral entropy of adsorption, 38 158, 160-161... 

Szanyi J and Goodman D W 1993 Combined elevated pressure reactor and ultrahigh vacuum surface analysis system Rev. Sci. Instrum. 64 2350... 

Instmmentation for tern is somewhat similar to that for sem however, because of the need to keep the sample surface as clean as possible throughout the analysis to avoid imaging surface contamination as opposed to the sample surface itself, ultrahigh vacuum conditions (ca 10 -10 Pa) are needed in the sample area of the microscope. Electron sources in tern are similar to those used in sem, although primary electron beam energies needed for effective tern are higher, typically on the order of ca 100 keV. 

Operationally, the electron techniques all require high-vacuum or, more likely, ultrahigh-vacuum environments, and the magnetic material of interest must be within a few atomic layers of the surface. MOKE analysis is not restricted by these constraints, although interesting samples may be. 

XPS Analysis. The ultrahigh vacuum (OHV) catalyst treatment-surface analysis system employed to characterize and treat the cobalt catalysts has been described previously ( 1, 2 The catalyst treatment and data analysis procedures have also been described (JJ. Briefly, the samples were treated in quartz reactors and then transferred under UHV into a modified Hewlett-Packard 5950A BSCA spectrometer for emalysis. Peak areas were normalized with theoretical cross-sections (Z) to obtain relative atomic compositions. 

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... 

GDS instruments are viable alternatives to the traditional arc and spark-source spectroscopies for bulk metals analysis. Advantages of GDS over surface analysis methods such as AES, XPS and SIMS are that an ultrahigh vacuum is not needed and the sputtering rate is relatively high. In surface analysis, GD-OES, AES, XPS and SIMS will remain complementary techniques. GD-OES analysis is faster than AES (typically 10 s vs. 15 min). GD-OES is also 100 times more sensitive than... 

There is a wealth of information available on CO chemisorption over single-crystal and polycrystalline platinum surfaces under ultrahigh-vacuum conditions research efforts in this area have gained a significant momentum with the advent of various surface analysis techniques (e.g., 2-8). In contrast, CO chemisorption on supported platinum catalysts (e.g., 9, 10, 11) is less well understood, due primarily to the inapplicability of most surface-sensitive techniques and to the difficulties involved in characterizing supported metal surfaces. In particular, the effects of transport resistances on the rates of adsorption and desorption over supported catalysts have rarely been studied. 

In conclusion, TDS of adsorbates on single crystal surfaces measured in ultrahigh vacuum systems with sufficiently high pumping speeds provides information on adsorbate coverage, the adsorption energy, the existence of lateral interactions between the adsorbates, and the preexponential factor of desorption, which in turn depends on the desorption mechanism. Analysis of spectra should be done with care, as simplified analysis procedures may easily give erroneous results. 

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