17.4 Potential, Free Energy, and Equilibrium

So far in this chapter, the relationship between the cell potential and reaction spontaneity has been described, suggesting a link to the free energy change for the reaction (see chapter on thermodynamics). The interpretation of potentials as measures of oxidant strength was presented, bringing to mind similar measures of acid-base strength as reflected in equilibrium constants (see the chapter on acid-base equilibria). This section provides a summary of the relationships between potential and the related thermodynamic properties ΔG and K.

E° and ΔG°

The standard free energy change of a process, ΔG°, was defined in a previous chapter as the maximum work that could be performed by a system, w $_{ma x}$ . In the case of a redox reaction taking place within a galvanic cell under standard state conditions, essentially all the work is associated with transferring the electrons from reductant-to-oxidant, w $_{e l ec}$ :

Δ G ° = w_{m a x} = w_{elec}

The work associated with transferring electrons is determined by the total amount of charge (coulombs) transferred and the cell potential:

Δ G ° = w_{elec} Δ G ° = = - n F E_{cell}^{°} - n F E_{cell}^{°}

where n is the number of moles of electrons transferred, F is Faraday’s constant, and E° $_{ce l l}$ is the standard cell potential. TFaraday's constant is defined as the charge in coulombs of one mole of electrons, F = 96,485 C/mol e–.he relation between free energy change and standard cell potential confirms the sign conventions and spontaneity criteria previously discussed for both of these properties: spontaneous redox reactions exhibit positive potentials and negative free energy changes.

E° and K

Combining a previously derived relation between ΔG° and K (see the chapter on thermodynamics) and the equation above relating ΔG° and E° $_{ce l l}$ yields the following:

Δ G ° E_{cell}^{°} = = - R T ln K = - n F E_{cell}^{°} (\frac{R T}{n F}) ln K

This equation indicates redox reactions with large (positive) standard cell potentials will proceed far towards completion, reaching equilibrium when the majority of reactant has been converted to product. A summary of the relations between E°, ΔG° and K is depicted in Figure 17.7, and a table correlating reaction spontaneity to values of these properties is provided in Table 17.2.

A diagram is shown that involves three double headed arrows positioned in the shape of an equilateral triangle. The vertices are labeled in red. The top vertex is labeled “K.“ The vertex at the lower left is labeled “delta G superscript degree symbol.” The vertex at the lower right is labeled “E superscript degree symbol subscript cell.” The right side of the triangle is labeled “E superscript degree symbol subscript cell equals ( R T divided by n F ) l n K.” The lower side of the triangle is labeled “delta G superscript degree symbol equals negative n F E superscript degree symbol subscript cell.” The left side of the triangle is labeled “delta G superscript degree symbol equals negative R T l n K.” — Figure 17.7Graphic depicting the relation between three important thermodynamic properties.

Table 17.2

K	ΔG°	E° $_{ce l l}$
> 1	< 0	> 0	Reaction is spontaneous under standard conditions Products more abundant at equilibrium
< 1	> 0	< 0	Reaction is non-spontaneous under standard conditions Reactants more abundant at equilibrium
= 1	= 0	= 0	Reaction is at equilibrium under standard conditions Reactants and products equally abundant

Potentials at Nonstandard Conditions: The Nernst Equation

Most of the redox processes that interest science and society do not occur under standard state conditions, and so the potentials of these systems under nonstandard conditions are a property worthy of attention. Having established the relationship between potential and free energy change in this section, the previously discussed relation between free energy change and reaction mixture composition can be used for this purpose.

Δ G = Δ G ° + R T ln Q

Notice the reaction quotient, Q, appears in this equation, making the free energy change dependent upon the composition of the reaction mixture. Substituting the equation relating free energy change to cell potential yields the Nernst equation:

- n F E_{cell} = - n F E_{cell}^{^{\circ}} + R T ln Q

E_{cell} = E_{cell}^{^{\circ}} - \frac{R T}{n F} ln Q

This equation describes how the potential of a redox system (such as a galvanic cell) varies from its standard state value, specifically, showing it to be a function of the number of electrons transferred, n, the temperature, T, and the reaction mixture composition as reflected in Q. A convenient form of the Nernst equation for most work is one in which values for the fundamental constants (R and F) and standard temperature (298) K), along with a factor converting from natural to base-10 logarithms, have been included:

E_{cell} = E_{cell}^{^{\circ}} - \frac{0.0592 V}{n} lo g Q

A concentration cell is constructed by connecting two nearly identical half-cells, each based on the same half-reaction and using the same electrode, varying only in the concentration of one redox species. The potential of a concentration cell, therefore, is determined only by the difference in concentration of the chosen redox species. The example problem below illustrates the use of the Nernst equation in calculations involving concentration cells.

Key Concepts and Summary

Potential is a thermodynamic quantity reflecting the intrinsic driving force of a redox process, and it is directly related to the free energy change and equilibrium constant for the process. For redox processes taking place in electrochemical cells, the maximum (electrical) work done by the system is easily computed from the cell potential and the reaction stoichiometry and is equal to the free energy change for the process. The equilibrium constant for a redox reaction is logarithmically related to the reaction’s cell potential, with larger (more positive) potentials indicating reactions with greater driving force that equilibrate when the reaction has proceeded far towards completion (large value of K). Finally, the potential of a redox process varies with the composition of the reaction mixture, being related to the reactions standard potential and the value of its reaction quotient, Q, as described by the Nernst equation.

Key Equations

E_{cell}^{^{\circ}} = \frac{R T}{n F} ln K