Nernst Equation
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The Nernst Equation enables the determination of cell potential under non-standard conditions. It relates the measured cell potential to the reaction quotient and allows the accurate determination of equilibrium constants (including solubility constants).
Introduction
The Nernst Equation is derived from the Gibbs free energy under standard conditions.
Eo=Eoreduction−Eooxidation
ΔG is also related to E under general conditions (standard or not) via
ΔG=−nFE
with
- n is the number of electrons transferred in the reaction (from balanced reaction),
- F is the Faraday constant (96,500 C/mol), and
- E is potential difference.
Under standard conditions, Equation ??? is then
ΔGo=−nFEo.
Hence, when Eo is positive, the reaction is spontaneous and when Eo is negative, the reaction is non-spontaneous. From thermodynamics, the Gibbs energy change under non-standard conditions can be related to the Gibbs energy change under standard Equations via
ΔG=ΔGo+RTlnQ
Substituting ΔG=−nFE and ΔGo=−nFEo into Equation ???, we have:
−nFE=−nFEo+RTlnQ
Divide both sides of the Equation above by −nF, we have
E=Eo−RTnFlnQ
Equation ??? can be rewritten in the form of log10:
E=Eo−2.303RTnFlog10Q
At standard temperature T = 298 K, the 2.303RTF term equals 0.0592 V and Equation ??? can be rewritten:
E=Eo−0.0592Vnlog10Q
The Equation above indicates that the electrical potential of a cell depends upon the reaction quotient Q of the reaction. As the redox reaction proceeds, reactants are consumed, and thus concentration of reactants decreases. Conversely, the products concentration increases due to the increased in products formation. As this happens, cell potential gradually decreases until the reaction is at equilibrium, at which ΔG=0. At equilibrium, the reaction quotient Q=Keq. Also, at equilibrium, ΔG=0 and ΔG=−nFE, so E=0.
Therefore, substituting Q=Keq and E=0 into the Nernst Equation, we have:
0=Eo−RTnFlnKeq
At room temperature, Equation ??? simplifies into (notice natural log was converted to log base 10):
0=Eo−0.0592Vnlog10Keq
This can be rearranged into:
logKeq=nEo0.0592V
The Equation above indicates that the equilibrium constant Keq is proportional to the standard potential of the reaction. Specifically, when:
- K>1,Eo>0, reaction favors products formation.
- K<1,Eo<0, reaction favors reactants formation.
This result fits Le Châtlier's Principle, which states that when a system at equilibrium experiences a change, the system will minimize that change by shifting the equilibrium in the opposite direction.
The Eocell=+1.10V for the Zn-Cu redox reaction:
Zn(s)+Cu2+(aq)⇌Zn2+(aq)+Cu(s).
What is the equilibrium constant for this reversible reaction?
SolutionUnder standard conditions, [Cu2+]=[Zn2+]=1.0M and T = 298 K. As the reaction proceeds, [Cu2+] decreases as [Zn2+] increases. Lets say after one minute, [Cu2+]=0.05M while [Zn2+]=1.95M. According to the Nernst Equation, the cell potential after 1 minute is:
E=Eo−0.0592VnlogQ
E=1.10V−0.0592V2log1.95M0.05M
E=1.05V
As you can see, the initial cell potential is E=1.10V, after 1 minute, the potential drops to 1.05 V. This is after 95% of the reactants have been consumed. As the reaction continues to progress, more Cu2+ will be consumed and more Zn2+ will be generated (at a 1:1 ratio). As a result, the cell potential continues to decrease and when the cell potential drops down to 0, the concentration of reactants and products stops changing.
This is when the reaction is at equilibrium. From from Equation 9, the Keq can be calculated from
logKeq=2×1.10V0.0592V=37.2
Keq=1037.2=1.58×1037
This make sense from a Le Châtlier's Principle, since the reaction strongly favors the products over the reactants to result in a large Eocell of 1.103 V. Hence, the cell is greatly out of equilibrium under standard conditions. Reactions that are just weakly out of equilibrium will have smaller Eocell values (neglecting a change in n of course).
References
- Atkins, Peter and de Paula, Julio. Physical Chemistry for the Life Sciences. New York: W.H. Freeman and Company. p. 214-222.
- Sherwood, Lauralee. Human Physiology 6th edition. Thompson Corp. 2007. p. 77
Outside Links
- Feiner, A.-S.; McEvoy, A. J. "The Nernst Equation." J. Chem. Educ. 1994, 71, 493.
- Thompson, Martin L.; Kateley, Laura J. "The Nernst Equation: Determination of Equilibrium Constants for Complex Ions of Silver." J. Chem. Educ. 1999 76 95.