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Metal photoelectrons

Electrochemistry Applications in Inorganic Chemistry Electronic Structure of Solids Heterogeneous Catalysis by Metals Photoelectron Spectroscopy of Transition Metal Systems Semiconductor Interfaces Thin Film Synthesis of Solids. [Pg.4751]

Ultraviolet photoelectron spectroscopy (UPS) results have provided detailed infomiation about CO adsorption on many surfaces. Figure A3.10.24 shows UPS results for CO adsorption on Pd(l 10) [58] that are representative of molecular CO adsorption on platinum surfaces. The difference result in (c) between the clean surface and the CO-covered surface shows a strong negative feature just below the Femii level ( p), and two positive features at 8 and 11 eV below E. The negative feature is due to suppression of emission from the metal d states as a result of an anti-resonance phenomenon. The positive features can be attributed to the 4a molecular orbital of CO and the overlap of tire 5a and 1 k molecular orbitals. The observation of features due to CO molecular orbitals clearly indicates that CO molecularly adsorbs. The overlap of the 5a and 1 ti levels is caused by a stabilization of the 5 a molecular orbital as a consequence of fomiing the surface-CO chemisorption bond. [Pg.951]

Wlien photons of sufiBciently high frequency v are directed onto a metal surface, electrons are emitted in a process known as photoelectron emission [ ]. The threshold frequency Vq is related to the work fimction by the expression... [Pg.1892]

Leopold D G, Ho J and Lineberger W C 1987 Photoelectron spectroscopy of mass-selected metal cluster anions. I. Cuji, n = 1 -10 J. Chem. Phys. 86 1715... [Pg.2401]

Concelcao J, Laaksonen R T, Wang L S, Guo T, Nordlander P and Smalley R E 1995 Photoelectron spectroscopy of transition metal clusters correlation of valence electronic structure to reactivity Rhys. Rev. B 51 4668... [Pg.2403]

Wang L S 2000 Photodetachment photoelectron spectroscopy of transition metal oxide species Photoionization and Photodetaohment Advanced Series in Physical Chemistry 10, ed C Y Ng (Singapore World Scientific)... [Pg.2407]

Using Equation (1.7) calculate the velocity of photoelectrons ejected from a sodium metal surface, with a work function of 2.46 eV, by ultraviolet light of wavelength 250 nm. [Pg.25]

Photoelectron spectroscopy involves the ejection of electrons from atoms or molecules following bombardment by monochromatic photons. The ejected electrons are called photoelectrons and were mentioned, in the context of the photoelectric effect, in Section 1.2. The effect was observed originally on surfaces of easily ionizable metals, such as the alkali metals. Bombardment of the surface with photons of tunable frequency does not produce any photoelectrons until the threshold frequency is reached (see Figure 1.2). At this frequency, v, the photon energy is just sufficient to overcome the work function

[Pg.289]

Rabalais, J. W. (1977) Principles of Ultraviolet Photoelectron Spectroscopy, John Wiley, New York. Roberts, M. W. and McKee, C. S. (1979) Chemistry of the Metal-Gas Interface, Oxford University Press, Oxford. [Pg.335]

NMR, 3, 542 oxidation, 3, 546 phosphorescence, 3, 543 photoelectron spectra, 3, 542 photolysis, 3, 549 reactions, 3, 543-555 with alkenes, 3, 50 with alkynes, 3, 50 with IH-azepines, 3, 552 with azirines, 3, 554 with cyclobutadiene, 3, 551 with cyclopropenes, 3, 550 with dimethylbicyclopropenyl, 3, 551 with heterocyclic transition metal complexes, 7, 28 29... [Pg.852]

An important property of the surface behaviour of oxides which contain transition metal ions having a number of possible valencies can be revealed by X-ray induced photoelectron spectroscopy. The energy spectrum of tlrese electrons give a direct measure of the binding energies of the valence electrons on the metal ions, from which the charge state can be deduced (Gunarsekaran et al., 1994). [Pg.125]

Figure 2 Molybdenum K-edge X-ray absorption spectrum, ln(i /i ) versus X-ray energy (eV), for molybdenum metal foil (25- jjn thick), obtained by transmission at 77 K with synchrotron radiation. The energy-dependent constructive and destructive interference of outgoing and backscattered photoelectrons at molybdenum produces the EXAFS peaks and valleys, respectively. The preedge and edge structures marked here are known together as X-ray absorption near edge structure, XANES and EXAFS are provided in a new compilation of literature entitled X-rsy Absorption Fine Structure (S.S. Hasain, ed.) Ellis Norwood, New York, 1991. Figure 2 Molybdenum K-edge X-ray absorption spectrum, ln(i /i ) versus X-ray energy (eV), for molybdenum metal foil (25- jjn thick), obtained by transmission at 77 K with synchrotron radiation. The energy-dependent constructive and destructive interference of outgoing and backscattered photoelectrons at molybdenum produces the EXAFS peaks and valleys, respectively. The preedge and edge structures marked here are known together as X-ray absorption near edge structure, XANES and EXAFS are provided in a new compilation of literature entitled X-rsy Absorption Fine Structure (S.S. Hasain, ed.) Ellis Norwood, New York, 1991.
An example of a spectrum with a chemical shift is that of the tin 3d peaks in Eig. 2.8. A thin layer of oxide on the metallic tin surface enables photoelectrons from both the underlying metal and the oxide to appear together. Resolution of the doublet 3 ds/2, 3 dii2 into the components from the metal (Sn ) and from the oxide Sn " is shown in Eig. 2.8 B. The shift in this instance is 1.6-1.7 eV. Curve resolution is an operation that can be performed routinely by data processing systems associated with photoelectron spectrometers. [Pg.16]

Surface analysis has made enormous contributions to the field of adhesion science. It enabled investigators to probe fundamental aspects of adhesion such as the composition of anodic oxides on metals, the surface composition of polymers that have been pretreated by etching, the nature of reactions occurring at the interface between a primer and a substrate or between a primer and an adhesive, and the orientation of molecules adsorbed onto substrates. Surface analysis has also enabled adhesion scientists to determine the mechanisms responsible for failure of adhesive bonds, especially after exposure to aggressive environments. The objective of this chapter is to review the principals of surface analysis techniques including attenuated total reflection (ATR) and reflection-absorption (RAIR) infrared spectroscopy. X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES), and secondary ion mass spectrometry (SIMS) and to present examples of the application of each technique to important problems in adhesion science. [Pg.243]

This method has already been used successfully for metallic iron. It presents several important advantages. It is a real space calculation for which no translational invariance is required. Calculation up to 500 eV above the edge can be performed because the basis set increases proportionally with the photoelectron energy. The separation between the three contributions (ai, Ojg and ajn) gives also new insight into the physics that is at the origin of XMCD. [Pg.463]

Recent developments in the mechanisms of corrosion inhibition have been discussed in reviews dealing with acid solutions " and neutral solu-tions - . Novel and improved experimental techniques, e.g. surface enhanced Raman spectroscopy , infrared spectroscopy. Auger electron spectroscopyX-ray photoelectron spectroscopyand a.c. impedance analysis have been used to study the adsorption, interaction and reaction of inhibitors at metal surfaces. [Pg.824]

In the following sections, results from various photoelectron spectroscopy studies of poly(p-pheny enevinylenc), polythiophene, and polyaniline, and their interaction with different metals will be discussed. The intention is not to cover the whole existing literature, but still give a relatively extensive overview, and, where appropriate, give references for further reading. [Pg.77]

In the many reports on photoelectron spectroscopy, studies on the interface formation between PPVs and metals, focus mainly on the two most commonly used top electrode metals in polymer light emitting device structures, namely aluminum [55-62] and calcium [62-67]. Other metals studied include chromium [55, 68], gold [69], nickel [69], sodium [70, 71], and rubidium [72], For the cases of nickel, gold, and chromium deposited on top of the polymer surfaces, interactions with the polymers are reported [55, 68]. In the case of the interface between PPV on top of metallic chromium, however, no interaction with the polymer was detected [55]. The results concerning the interaction between chromium and PPV indicates two different effects, namely the polymer-on-metal versus the metal-on-polymer interface formation. Next, the PPV interface formation with aluminum and calcium will be discussed in more detail. [Pg.78]

Table 8 shows results obtained from the application of various bulk and surface analysis methods to lithium metal at rest or after cyclization experiments, as well as at inert and carbon electrodes after cathodic polarization. The analytical methods include elemental analysis, X-ray photoelectron spectroscopy (XPS or ESCA), energy-dispersive analysis of X-rays (X-ray mi-... [Pg.481]


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See also in sourсe #XX -- [ Pg.262 ]




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Alkali metals photoelectrons from

Photoelectron metal oxide surfaces

Photoelectron spectroscopy applied polymer-metal interactions

Titanium metal, photoelectron

UV photoelectron spectroscopy, in transition metal chemistry

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