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Vacuum spectroscopy

Electrons are extremely usefiil as surface probes because the distances that they travel within a solid before scattering are rather short. This implies that any electrons that are created deep within a sample do not escape into vacuum. Any technique that relies on measurements of low-energy electrons emitted from a solid therefore provides infonuation from just the outenuost few atomic layers. Because of this inlierent surface sensitivity, the various electron spectroscopies are probably the most usefid and popular teclmiques in surface science. [Pg.305]

Continuous wave (CW) lasers such as Ar and He-Ne are employed in conmionplace Raman spectrometers. However laser sources for Raman spectroscopy now extend from the edge of the vacuum UV to the near infrared. Lasers serve as an energetic source which at the same hme can be highly monochromatic, thus effectively supplying the single excitation frequency, v. The beams have a small diameter which may be... [Pg.1199]

Because of the generality of the symmetry principle that underlies the nonlinear optical spectroscopy of surfaces and interfaces, the approach has found application to a remarkably wide range of material systems. These include not only the conventional case of solid surfaces in ultrahigh vacuum, but also gas/solid, liquid/solid, gas/liquid and liquid/liquid interfaces. The infonnation attainable from the measurements ranges from adsorbate coverage and orientation to interface vibrational and electronic spectroscopy to surface dynamics on the femtosecond time scale. [Pg.1265]

Perhaps the best known and most used optical spectroscopy which relies on the use of lasers is Raman spectroscopy. Because Raman spectroscopy is based on the inelastic scattering of photons, the signals are usually weak, and are often masked by fluorescence and/or Rayleigh scattering processes. The interest in usmg Raman for the vibrational characterization of surfaces arises from the fact that the teclmique can be used in situ under non-vacuum enviromnents, and also because it follows selection rules that complement those of IR spectroscopy. [Pg.1786]

Hepburn J W 1995 Generation of coherent vacuum ultraviolet radiation applications to high-resolution photoionization and photoelectron spectroscopy Laser Techniques in Chemistry vol 23, ed A B Myers and T R Rizzo (New York Wley) pp 149-83... [Pg.2088]

Elemental chemical analysis provides information regarding the formulation and coloring oxides of glazes and glasses. Energy-dispersive x-ray fluorescence spectrometry is very convenient. However, using this technique the analysis for elements of low atomic numbers is quite difficult, even when vacuum or helium paths are used. The electron-beam microprobe has proven to be an extremely useful tool for this purpose (106). Emission spectroscopy and activation analysis have also been appHed successfully in these studies (101). [Pg.422]

Oxygen and nitrogen also are deterrnined by conductivity or chromatographic techniques following a hot vacuum extraction or inert-gas fusion of hafnium with a noble metal (25,26). Nitrogen also may be deterrnined by the Kjeldahl technique (19). Phosphoms is determined by phosphine evolution and flame-emission detection. Chloride is determined indirecdy by atomic absorption or x-ray spectroscopy, or at higher levels by a selective-ion electrode. Fluoride can be determined similarly (27,28). Uranium and U-235 have been determined by inductively coupled plasma mass spectroscopy (29). [Pg.443]

Lead Telluride. Lead teUuride [1314-91 -6] PbTe, forms white cubic crystals, mol wt 334.79, sp gr 8.16, and has a hardness of 3 on the Mohs scale. It is very slightly soluble in water, melts at 917°C, and is prepared by melting lead and tellurium together. Lead teUuride has semiconductive and photoconductive properties. It is used in pyrometry, in heat-sensing instmments such as bolometers and infrared spectroscopes (see Infrared technology AND RAMAN SPECTROSCOPY), and in thermoelectric elements to convert heat directly to electricity (33,34,83). Lead teUuride is also used in catalysts for oxygen reduction in fuel ceUs (qv) (84), as cathodes in primary batteries with lithium anodes (85), in electrical contacts for vacuum switches (86), in lead-ion selective electrodes (87), in tunable lasers (qv) (88), and in thermistors (89). [Pg.69]

Shorter-wavelength radiation promotes transitions between electronic orbitals in atoms and molecules. Valence electrons are excited in the near-uv or visible. At higher energies, in the vacuum uv (vuv), inner-shell transitions begin to occur. Both regions are important to laboratory spectroscopy, but strong absorption by make the vuv unsuitable for atmospheric monitoring. Electronic transitions in molecules are accompanied by stmcture... [Pg.311]

J. A. R. Sampson, Techniques of Vacuum Ultraviolet Spectroscopy,JohnWHey 8c Sons, Inc., New York, 1967. [Pg.324]

A. N. Zaidef and E. Ya. Shreider, Vacuum Ultraviolet Spectroscopy, Humphrey Science PubHshers, Ann Arbor, Mich., 1970. [Pg.324]

Occasionally, especially in the developmental phase of catalyst research, it is necessary to determine the oxidation state, exact location, and dispersion of various elements in the catalyst. Eor these studies, either transmission electron microscopy (TEM) or scanning electron microscopy (SEM) combined with various high vacuum x-ray, electron, and ion spectroscopies are used routinely. [Pg.196]

Another basic approach of CL analysis methods is that of the CL spectroscopy system (having no electron-beam scanning capability), which essentially consists of a high-vacuum chamber with optical ports and a port for an electron gun. Such a system is a relatively simple but powerful tool for the analysis of ion implantation-induced damage, depth distribution of defects, and interfaces in semiconductors. ... [Pg.154]


See other pages where Vacuum spectroscopy is mentioned: [Pg.23]    [Pg.440]    [Pg.23]    [Pg.440]    [Pg.2]    [Pg.689]    [Pg.200]    [Pg.248]    [Pg.302]    [Pg.1119]    [Pg.1125]    [Pg.1179]    [Pg.1264]    [Pg.1779]    [Pg.1807]    [Pg.1828]    [Pg.1868]    [Pg.2439]    [Pg.286]    [Pg.66]    [Pg.167]    [Pg.172]    [Pg.451]    [Pg.397]    [Pg.177]    [Pg.398]    [Pg.615]    [Pg.304]    [Pg.2]    [Pg.9]    [Pg.13]    [Pg.25]    [Pg.38]    [Pg.157]    [Pg.300]    [Pg.372]    [Pg.391]    [Pg.473]    [Pg.724]    [Pg.255]   
See also in sourсe #XX -- [ Pg.188 , Pg.191 ]

See also in sourсe #XX -- [ Pg.144 ]

See also in sourсe #XX -- [ Pg.243 ]




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Combination of electrochemistry with vacuum spectroscopy

Ultra high vacuum spectroscopy

Ultra-high vacuum Photoelectron spectroscopy

Ultrahigh vacuum surface spectroscopy

Ultrahigh-vacuum spectroscopy, effect

Vacuum UV spectroscopy

Vacuum Ultraviolet Photoelectron Spectroscopy of Inorganic Molecules

Vacuum ultraviolet photoelectron spectroscopy

Vacuum ultraviolet spectroscopy

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