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Valence level

When the states P1 and P2 are described as linear combinations of CSFs as introduced earlier ( Fi = Zk CiKK), these matrix elements can be expressed in terms of CSF-based matrix elements < K I eri IOl >. The fact that the electric dipole operator is a one-electron operator, in combination with the SC rules, guarantees that only states for which the dominant determinants differ by at most a single spin-orbital (i.e., those which are "singly excited") can be connected via electric dipole transitions through first order (i.e., in a one-photon transition to which the < Fi Ii eri F2 > matrix elements pertain). It is for this reason that light with energy adequate to ionize or excite deep core electrons in atoms or molecules usually causes such ionization or excitation rather than double ionization or excitation of valence-level electrons the latter are two-electron events. [Pg.288]

Other techniques in which incident photons excite the surface to produce detected electrons are also Hsted in Table 1. X-ray photoelectron Spectroscopy (xps), which is also known as electron spectroscopy for chemical analysis (esca), is based on the use of x-rays which stimulate atomic core level electron ejection for elemental composition information. Ultraviolet photoelectron spectroscopy (ups) is similar but uses ultraviolet photons instead of x-rays to probe atomic valence level electrons. Photons are used to stimulate desorption of ions in photon stimulated ion angular distribution (psd). Inverse photoemission (ip) occurs when electrons incident on a surface result in photon emission which is then detected. [Pg.269]

Yes, but complicated using valence levels for core levels as for XPS... [Pg.23]

In some cases, a valence electron can be completely ionized, resulting in vacancies in both the core and valence levels. In those cases, weak peaks referred to as shake-off satellites are also observed at binding energies a few electron volts higher than the photoelectron peak. Such cases are, however, not very common. [Pg.264]

M and M both covered by backspillover O ions and exposed to two different p02 values under open-circuit conditions. How do p,02> P02- and p (=Ep) vary across the cell And how do they relate to the conduction level Ec and valence level Ev of YSZ ... [Pg.356]

Figure 7.13. The definitions of ionization potential, Ie, work function, , Fermi level, EF, conduction level, Ec, valence level Ev, and x-potential Xe without (a) and with (b) band bending at the semiconductor-vacuum interface. Figure 7.13. The definitions of ionization potential, Ie, work function, <t>, Fermi level, EF, conduction level, Ec, valence level Ev, and x-potential Xe without (a) and with (b) band bending at the semiconductor-vacuum interface.
Figure 6.24. Interaction between an atomic adsorbate with one valence level and a transition metal, which possesses a broad sp band and a narrow d band located at the Fermi level. The strong interaction with the d band... Figure 6.24. Interaction between an atomic adsorbate with one valence level and a transition metal, which possesses a broad sp band and a narrow d band located at the Fermi level. The strong interaction with the d band...
Here, we demonstrate clear and direct evidence for the modified electronic structures of surface Pt atoms in Pt-Co and Pt-Ru by using EC-XPS [Wakisaka et al., 2006]. The sample electrode was transferred between an XPS chamber and an electrochemical (EC) chamber without exposure to air (to minimize contamination of the surface). All photoelectron spectra, including the valence level region) were taken by using a monochromatic Al Ka (hv = 1486.58 eV). The uncertainty of binding energy measurement was less than + 0.03 eV. [Pg.323]

Extensive discussion on the ionization potentials of 1,2,5-thiadiazole and its derivatives can be found in CHEC(1984) and CHEC-II(1996) <1984CHEC(6)513, 1996CHEC-II(4)355>. Hel photoelectron spectroscopy, inner-shell electron energy loss spectroscopy involving the S2p, S2s, Cls and Nls edges, and Sis synchrotron radiation photoabsorption spectroscopy were used to probe the occupied and unoccupied valence levels of benzothiadiazole 2 <1991MI165>. [Pg.523]

Conductivity means that an electron moves under the influence of an applied field, which implies that field energy transferred to the electron promotes it to a higher level. Should the valence level be completely filled there are no extra higher-energy levels available in that band. Promotion to a higher level would then require sufficient energy to jump across the gap into a conduction level in the next band. The width of the band gap determines whether the solid is a conductor, a semi-conductor or an insulator. It is emphasized that in three-dimensional solids the band structure can be much more complicated than for the illustrative one-dimensional model considered above and could be further complicated by impurity levels. [Pg.325]

The HFS program [79] was modified especially for this purpose. The general response is the same as for hydrogen, except that all occupied levels are now also affected at the same time. The highest levels are the most sensitive, but even the deepest core levels show an increase. As for hydrogen, the valence level eventually reaches the ionization limit, but this cannot be interpreted directly as an ionization event, as was done for hydrogen. [Pg.359]


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See also in sourсe #XX -- [ Pg.285 ]




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