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Zero-level energy

This is a thermodynamically legitimate choice of the zero energy level and she potentials are the ones most commonly used in aqueous... [Pg.334]

Figure 7.1. Definition of absolute electron potential in aqueous electrochemistry according to Trasatti16 in a classical (a) and liquid covered (b) electrode geometry. Point C corresponds to the zero energy level. O0 is the work function of the bare electrode surface and AC>(=eA P) is the work function modification induced by the presence of the electrolyte layer (b). Reprinted with permission from Elsevier Science. Figure 7.1. Definition of absolute electron potential in aqueous electrochemistry according to Trasatti16 in a classical (a) and liquid covered (b) electrode geometry. Point C corresponds to the zero energy level. O0 is the work function of the bare electrode surface and AC>(=eA P) is the work function modification induced by the presence of the electrolyte layer (b). Reprinted with permission from Elsevier Science.
It is worth noting in Figures 7. lb and 7.2b that the zero energy level choice (point C) is not only, by definition, a point in vacuum close to the surface of the solution (Fig. 7.1a, 7.2a), but also, as clearly shown by Trasatti,16 a point in vacuum close to the surface of the emersed (liquid or adsorption covered) electrode. [Pg.336]

This, at first perhaps surprising fact, is important to remember as the same situation arises in solid state electrochemistry. To understand its validity it suffices to remember that the definition of the reference (zero) energy level of electrons for the she scale is simply the state of an electron at the Fermi level of any metal in equilibrium with an aqueous solution of pH=0 and pH2=l atm at 25°C. [Pg.336]

The ionization energy, Ie, for YSZ is 7.14 eV. This defines the location of the valence band, Ey, in relation to the zero energy level. [Pg.357]

Fig. 9. Calculated relative energies (in kK) of the most important MO s (a) and spectral excitation energies derived from the electronic absorption spectrum (b) of ClFe(Et2 Fig. 9. Calculated relative energies (in kK) of the most important MO s (a) and spectral excitation energies derived from the electronic absorption spectrum (b) of ClFe(Et2<ifc)2- The zero energy level points are taken arbitrarily. For the numbering of the MO s see ref. 61).
The isolated rest state of a given particle at infinity in vacuum (temperature T) This zero energy level is used in physics. The rest state of a particle is hypothetical having the energy only due to the internal freedom of particles. We call the rest electron the vacuum electron, e< ao, and its energy the vacuum electron level, = 0. [Pg.8]

Assuming that an isolated gaseous ion X is at the reference zero energy level as shown in Fig. 3-1, we define the occupied energy level of X ion (the unitary X ion donor level, molecule XY by the negative ionic dissociation... [Pg.61]

The ion level in condensed phases has been represented by the real potential, a, referred to the standard gaseous state of the ion at the outer potential of the condensed phases. The reference level, then, is not common to all ions but differs with different ions. In chemical thermodynamics, the conventional energy scale is based on the assumption that all atoms in the stable form in the standard state are at the zero energy level, which is the thermodynamic reference level of energy for chemical substances. In the following, we discuss the relationship between the scale of the ion level represented by the real potential of ions and the conventional energy scale of particles in chemical thermodynamics. [Pg.85]

Near the ionization limit (E —> 0) the bound-state levels become increasingly closely spaced and the valence electron can be activated 3 virtually continuously towards the zero energy level. At this level... [Pg.160]

The partition functions are given in eq. (3.11) with respect to the same zero energy level. Taking into account the energy difference between ground state and the transition sate we have instead of eq. (3.11)... [Pg.77]

In Fig. 3.4, the ground state is shown as having negative energy to indicate a bound state. The ground state and all the excited states below the zero energy level are called bound states. If the nucleus finds itself in any of the bound... [Pg.91]

Typical potential ener r diagrams that might be expected for simple combinations of depletion stabilization with steric or electrostatic stabilization are displayed in Fig. 17.14. The minimum in the potential enCTgy curve need not be below the zero energy level in order to induce weak flocculation, although it would be expected that this type of behaviour would be rare and depend upon the specific details of the system in question. [Pg.399]

D is the absolute dissociation limit for the C l, 5 1, and 0" potentials with respect to the ground state zero energy level. [Pg.211]

NEA photocathodes are photoconductive semiconductors whose surface has been treated to obtain a state of negative electron affinity . This state is reached when the energy level of an electron at the bottom of the conduction band in the bulk of the semiconductor is greater than the zero energy level of an electron in the vacuum. Hence an electron excited to the conduction band within the bulk can, if it travels to the activated surface without first recombining, energetically fall out of the photocathode into free space. [Pg.165]

Theorem % The eigenvalues of an alternant are symmetrically distributed about the zero energy level. The corresponding eigenfunctions also show a mirror relationship, except for a difference of sign (only) in every other atomic orbital coefficient. The total charge density at any carbon atom in the neutral alternant hydrocarbon equals unity. [Pg.97]


See other pages where Zero-level energy is mentioned: [Pg.14]    [Pg.362]    [Pg.352]    [Pg.352]    [Pg.238]    [Pg.217]    [Pg.221]    [Pg.280]    [Pg.125]    [Pg.35]    [Pg.435]    [Pg.59]    [Pg.403]    [Pg.404]    [Pg.407]    [Pg.408]    [Pg.11]    [Pg.86]    [Pg.67]    [Pg.59]    [Pg.113]    [Pg.92]    [Pg.15]    [Pg.490]    [Pg.498]    [Pg.202]    [Pg.301]    [Pg.126]    [Pg.202]    [Pg.266]    [Pg.74]    [Pg.2]   
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