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Inner work function

Figure 5.7. Schematic representation of the definitions of work function O, chemical potential of electrons i, electrochemical potential of electrons or Fermi level p = EF, surface potential %, Galvani (or inner) potential Figure 5.7. Schematic representation of the definitions of work function O, chemical potential of electrons i, electrochemical potential of electrons or Fermi level p = EF, surface potential %, Galvani (or inner) potential <p, Volta (or outer) potential F, Fermi energy p, and of the variation in the mean effective potential energy EP of electrons in the vicinity of a metal-vacuum interface according to the jellium model. Ec is the bottom of the conduction band and dl denotes the double layer at the metal/vacuum interface.
A somewhat curious effect arises when additional water is dosed on top of this synthetic inner layer, in that the work function is observed to exhibit substantial further decreases. This implies that the water molecules in the multilayers above the inner layer assume some measure of preferential orientation, induced by the presence of the adsorbed bromide in the first layer. This result is probably connected to structure making and structure breaking, or hydrophobic and hydrophilic, properties of soild surfaces, but will not be discussed in detail here. [Pg.59]

Figure 3. Work function change for a) bromine on Ag 110 b) bromine and hydration water c) bromine and water to complete the inner layer d) bromine and multilayers of water. Figure 3. Work function change for a) bromine on Ag 110 b) bromine and hydration water c) bromine and water to complete the inner layer d) bromine and multilayers of water.
Figure4. Comparison of UHV and in situ electrochemical data. Solid and dotted lines correspond to the potential drop across the inner layer for the Br/H20 and Cl / H2O systems at a Ag 110 electrode. Full circles correspond to the change in work function of a Ag l 10 surface with Br and water to complete the inner layer (taken from figure 3 c). Open triangles correspond to similar work function data for the Cl / H2O system on Ag l 10. ... Figure4. Comparison of UHV and in situ electrochemical data. Solid and dotted lines correspond to the potential drop across the inner layer for the Br/H20 and Cl / H2O systems at a Ag 110 electrode. Full circles correspond to the change in work function of a Ag l 10 surface with Br and water to complete the inner layer (taken from figure 3 c). Open triangles correspond to similar work function data for the Cl / H2O system on Ag l 10. ...
Figure 2. Work function of polycrystalline Au electrode emersed from 0.1 M HC104 as a function of emersion potential. The work function of the clean metal surface was 5.2 eV (19). If the NHE absolute half-cell potential (with respect to s) is 4.45 V, the bottom line is equal to the solution inner potential, tfg. If it is 4.85 V, the upper curve through the points is equal to 0g. As always with WF, the Fermi level is taken as zero. Figure 2. Work function of polycrystalline Au electrode emersed from 0.1 M HC104 as a function of emersion potential. The work function of the clean metal surface was 5.2 eV (19). If the NHE absolute half-cell potential (with respect to <t>s) is 4.45 V, the bottom line is equal to the solution inner potential, tfg. If it is 4.85 V, the upper curve through the points is equal to 0g. As always with WF, the Fermi level is taken as zero.
Double layer emersion continues to allow new ways of studying the electrochemical interphase. In some cases at least, the outer potential of the emersed electrode is nearly equal to the inner potential of the electrolyte. There is an intimate relation between the work function of emersed electrodes and absolute half-cell potentials. Emersion into UHV offers special insight into the emersion process and into double layer structure, partly because absolute work functions can be determined and are found to track the emersion potential with at most a constant shift. The data clearly call for answers to questions involving the most basic aspects of double layer theory, such as the role water plays in the structure and the change in of the electrode surface as the electrode goes frcm vacuum or air to solution. [Pg.172]

In the case of nonpolaiizable interfaces, the inner and the outer potential differences, 4>a/b and v a/b, are determined by the equilibrium of chai transfer that occurs across the interface. Figure 4—8 shows the electron energy levels in two sohd metals A and B before and after they are brought into contact with each other. As a result of contact, electrons in a metal B of the hi er electron level (the lower work function ) move into a metal A of the lower electron level (the higher work fiuiction), and the Fermi levels of the two metals finally become equal to each other in the state of electron transfer equilibrium. The electrochemical... [Pg.94]

When two isolated and electrically neutral conductors A and B with electrochemical potentials fiA and /la, respectively, are placed in electrical contact, iiA and fLa change in value so that at equilibrium fiA = Ms. This effect is due to the transfer of electrons from the conductor with the higher electrochemical potential until (0 — inner is equal to the initial difference Ha — Mb, Mi the chemical potential, being insensitive to variations in electron density. Thus from Equation (1) it follows that an electrical potential difference Vab, equal to (0 — 0B)outor > and hence to the difference in work function A, appears between points just outside the surface of the two conductors, i.e.,... [Pg.76]

Define the following terms used in Section 6.3 (a) electrochemical cell, (b) ideally nonpolarizable and polarizable interfaces, (c) relative electrode potential, (d) outer potential, (e) inner potential, (1) surface potential, (g) image forces, (h) Coulombic forces, (i) electrochemical potential, (j) chemical potential, (k) electron work function, (1) just outside the metal, and (m) absolute potential. (Gamboa-Aldeco)... [Pg.299]

If some or all of the ensemble conformations reveal actual alternative conformations in solution, then these models contain useful information that may be lost in producing the averaged model. If the most important conformations for molecular function are represented in subsets of models within the final ensemble, then an averaged model may mislead us about function. Just like crystallographic models, NMR models do not simply tell us what we would like to know about the inner workings of molecules. Evidence from other areas of research on the molecule are necessary in interpreting what NMR models have to say. [Pg.237]

Here (p is the inner electrostatic potential of the bulk, % is the dipole surface potential, and t f is the outer electrostatic potential. For y/ 0, the work function consists... [Pg.355]

To better understand the structure and the inner workings of an environmental laboratory, we need to familiarize ourselves with laboratory functional groups and their responsibilities. Figure 4.2 shows an example of a typical full service environmental laboratory organization chart. A full service laboratory has the capabilities to perform analysis for common environmental contaminants, such as VOCs and SVOCs (including petroleum fuels and their constituents, pesticides, herbicides, and PCBs), trace elements (metals), and general chemistry parameters. Analysis of dioxins/furans, explosives, radiochemistry parameters, and analysis of contaminants in air are not considered routine, and are performed at specialized laboratories. [Pg.186]

DNA base pairs containing an estimated 20,000 -25,000 genes.3,4 Each gene codes for a protein, and these proteins carry out all the functions of the human body, laying out how it grows and works. These genes and proteins can also be involved in disease. Hence, scientists are able to understand the inner workings of human disease at both the tissue level and the molecular level. [Pg.6]

In studies on electron diffraction, however,-yet another potential is considered, called the mean inner potential . The metal may be considered as a potential box, the distance of the uppermost level below the potential just outside the metal, V, the electrostatic potential already referred to, being equal to x> the thermionic work function. The lowest level (at low temperatures) is, according to the new statistics, a distance below the upper equal to [/1], where... [Pg.306]


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See also in sourсe #XX -- [ Pg.572 ]




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