Author: admin
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Impact of Potential on Reaction Rate
Electrochemical reactions take place at the surface of the electrode as electrons are transferred to and from ions or neutral species in solution. The rate of reaction is influenced by the potential drop across the double layer. At open circuit (no external current), this potential drop reaches an equilibrium value where the forward and reverse…
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Double Layer
A metal electrode in an electrolyte solution is typically charged, even at equilibrium. Excess charge is present on the outer surface of the electrode, adjacent to the electrode–electrolyte interface. The amount of charge in the metal electrode is a measure of the energy of the electrons in the metal and can be changed by using…
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Estimation of Activity Coefficients
In dilute solutions, long-range electrical interactions between ions dominate, and the activity coefficient can be estimated from a determination of the electrical contribution alone. The chemical potential is equal to the reversible work of transferring 1 mol of the species to a large volume of the solution at constant temperature and pressure. The nonideal portion…
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Activities and Activity Coefficients
The accuracy of our expression for cell potential can be increased by including the full activity corrections, rather than the approximations used earlier. The complexity of the calculations, however, increases significantly. The treatment below assumes that the reader has been exposed to the concepts of activity and fugacity. If these are new to you, you…
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Potential in Solution Due to Charge: Debye–Hückel Theory
The previous section described a potential difference between a surface and the adjacent solution. This potential difference is due to unbalanced charge in solution as a result of charge on a surface or on an ion. Both of these situations (surface and ion) have been described in the literature using very similar approaches, and the…
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Equilibrium at Electrode Interface
In this chapter, we have shown how to calculate the thermodynamic potential and the relationship between this equilibrium value and the change in the Gibbs energy for the full-cell reaction. We have also referred to this potential as an equilibrium potential. Clearly, however, the full-cell reaction is not in equilibrium, which would mean that ΔGRx = 0.…
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Reference Electrodes
The potential scale in Appendix A is based on the SHE. This scale is arbitrary, and by convention is taken to be zero at standard state as mentioned previously. For experimental work it is generally desirable to have a reference electrode in the system. The purpose of the reference electrode is to provide a known, stable potential…
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Cells with a Liquid Junction
The Daniell cell that was examined previously presupposed a selectively permeable membrane separator. In practice, simple porous media are often used. In this case, bulk mixing is avoided, but ions are able to move between electrodes. In fact, we often have electrochemical cells where the two electrodes are in solutions of different concentration and/or composition.…
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Pourbaix Diagrams
A knowledge of the equilibrium potential for reactions involving a specified set of elements allows us to determine the species that are thermodynamically stable under a particular set of conditions. A common way to present such data in aqueous media is with a Pourbaix diagram, which has been particularly useful for studying corrosion. For example,…
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Use of the Cell Potential
Now that we have a way of determining the equilibrium potential, let’s look at how we can use it. First, the convention we have adopted tells us that when the circuit is closed, a spontaneous reaction will occur. More specifically, a cathodic or reduction reaction takes place on the positive electrode, and an anodic or…