The Nernst equation | Applications of thermodynamics | AP Chemistry | Khan Academy
We already know how to calculate cell potential when the reactants and products are in their standard states. However, what if that's not the case? We can find cell potential when reactants and products are not in their standard states by using the Nernst equation, which is shown here, and we're going to call that cell potential the instantaneous cell potential.
E_cell is the instantaneous cell potential, the cell potential or voltage at a specific moment in time. E_naught of the cell is the standard cell potential. This is the cell potential when the reactants and products are in their standard states. R is the ideal gas constant, T is the temperature, n is the number of electrons transferred in the redox reaction, F is Faraday's constant, and Q is the reaction quotient.
So this is one way to write the Nernst equation, and let's compare this form of the Nernst equation to a simplified form. In the simplified form of the Nernst equation, E_cell is equal to E_naught of the cell minus 0.0592 volts divided by n times the log of the reaction quotient Q.
Going back to the first form of the Nernst equation, if we assume the temperature is 25 degrees Celsius or 298 Kelvin, we multiply that by the ideal gas constant, divide that by Faraday's constant, and if we're changing natural log to log, then we end up with this form for the bottom equation: 0.0592 volts divided by n times the log of Q.
For this second term of the Nernst equation, you can use the Nernst equation to quantitatively calculate the exact voltage at a specific moment in time. However, we're going to try to think about the Nernst equation from a qualitative point of view.
Let's use the Nernst equation to think about the instantaneous cell potential for a zinc-copper cell, and we're going to look at a few different situations. In a zinc-copper cell, solid zinc is oxidized to zinc two plus ions, and copper two plus ions are reduced to form solid copper. The standard cell potential for the zinc-copper cell at 25 degrees Celsius is equal to positive 1.10 volts.
Our goal is to find the cell potential at the moment in time when the concentration of copper two plus ions is equal to 1.0 molar and the concentration of zinc two plus ions in solution is also equal to 1.0 molar. To find the instantaneous cell potential, we're going to use the simplified form of the Nernst equation. E_naught of the cell is equal to positive 1.10 volts.
Next, let's think about n, the number of electrons transferred in the redox reaction. Looking at our equation here, solid zinc going to zinc two plus is loss of two electrons, and copper two plus going to solid copper is a gain of two electrons. So, two electrons were transferred, and n is equal to two. I've gone ahead and made n equal to two in our equation.
Next, we need to think about the reaction quotient Q. Q has the same form as the equilibrium constant expression. So, if we think about the balanced equation, remember pure solids are left out of equilibrium constant expressions. Therefore, Q is equal to the concentration of zinc two plus ions divided by the concentration of copper two plus ions. Since our goal is to find the instantaneous cell potential when the concentrations are both equal to one molar, Q is equal to one divided by one, so Q is equal to one.
The log of one is equal to zero; therefore, this entire second term in the Nernst equation is equal to zero, which means the instantaneous cell potential is equal to the standard cell potential. So, the instantaneous cell potential is equal to positive 1.10 volts. This answer makes a lot of sense because standard state for solutions is a one molar concentration. Therefore, the instantaneous cell potential is equal to the standard cell potential at this moment in time.
Next, let's think about the instantaneous cell potential when the concentration of copper two plus ions is equal to 10.0 molar and the concentration of zinc two plus ions is equal to 1.0 molar. The standard cell potential at 25 degrees Celsius is still equal to positive 1.10 volts, and n is still equal to 2. So, we need to think about the reaction quotient Q at this moment in time. The concentration of zinc two plus ions is equal to 1.0 molar, so we plug that in, and the concentration of copper two plus ions is equal to 10.0 molar.
At this moment in time, Q is less than one. The log of a number less than 1 is negative; therefore, this second term would be negative or less than 0. Since we are subtracting a negative number, we would actually be adding that value to the standard cell potential. This means that the instantaneous cell potential will be greater than the standard cell potential. If you went ahead and calculated the instantaneous cell potential with the Nernst equation, you would find it's equal to positive 1.13 volts, which is greater than positive 1.10 volts.
Next, let's think about the instantaneous cell potential when the concentration of copper two plus ions is equal to 1.0 molar and the concentration of zinc two plus ions is equal to 10.0 molar. According to the Nernst equation, the standard cell potential is still positive 1.10 volts, and n is still equal to 2.
Next, we think about the reaction quotient Q. At this moment in time, the concentration of zinc two plus ions is equal to 10.0 molar, and the concentration of copper two plus ions is equal to 1.0 molar. So at this moment in time, Q is greater than one. The log of a number greater than one is positive; therefore, the second term in our equation will be positive or greater than zero. Because we are subtracting a positive number, we would be subtracting a value from the standard cell potential. This means that the instantaneous cell potential will be less than the standard cell potential.
If you plug the numbers into the Nernst equation, you would find that the instantaneous cell potential is equal to positive 1.07 volts, which is less than the standard cell voltage of 1.10 volts. We just observed that at the moment in time when the concentration of copper two plus ions is equal to 1.0 molar and the concentration of zinc two plus ions is equal to 10.0 molar, the instantaneous cell potential is equal to positive 1.07 volts.
Let's use this moment in time as a starting point and think about what happens to the instantaneous cell potential as the reaction progresses. Remember that the instantaneous cell potential is related to the instantaneous change in free energy ΔG by this equation: ΔG is equal to negative nFE. Because we have a positive value for the instantaneous cell potential, if we plug in a positive value into our equation, because of the negative sign in the equation, we would get a negative sign for ΔG.
When ΔG is negative, the reaction is thermodynamically favored, which means the reactants will turn into products. As the reactants turn into products, the concentration of zinc two plus ions will increase, and the concentration of copper two plus ions will decrease. Think about what that does to the reaction quotient Q. There would be an increase in the concentration of zinc two plus ions and a decrease in the concentration of copper two plus ions, so Q would no longer be equal to 10.0 over 1.0. We would see an increase in Q as the reactants turn into the products.
An increased value of Q means that the second term in the Nernst equation will be a larger positive number. So if we subtract a larger positive number than we did in the previous example from the standard cell potential, we would get a lower instantaneous cell potential than positive 1.07 volts.
What the Nernst equation tells us is, as the reaction goes to the right, there's an increase in Q, and as Q increases, there's a decrease in the instantaneous cell potential. So we've just observed that as the reaction goes to the right, there's an increase in Q, and according to the Nernst equation, that's a decrease in the instantaneous cell potential. Therefore, the instantaneous cell potential would decrease from 1.07 volts.
However, the voltage would still be positive, which means that ΔG would still be negative, indicating that the reaction is still thermodynamically favored. This keeps happening as the reaction goes to the right; Q keeps increasing, and the instantaneous cell potential keeps decreasing.
We had started out at positive 1.07 volts, and we saw that it had decreased, and it keeps on decreasing. Eventually, the instantaneous cell potential will go to zero volts. When the voltage goes to 0, if you plug in 0 into our equation, ΔG is equal to 0. When ΔG is equal to 0, the reaction is at equilibrium, and the reaction quotient Q is equal to the equilibrium constant K.
So, if you were to plug in the equilibrium constant K in for Q, you would find that this entire second term would be equal to positive 1.10 volts and cancel out the standard cell potential, giving an instantaneous potential of zero volts.
So, if we think about our zinc-copper cell as a battery, when the reaction reaches equilibrium, the voltage is equal to zero, and the battery is dead.
Let's do a quick summary of what we've learned from the Nernst equation. This is the simplified form, which is valid at 25 degrees Celsius:
When Q is equal to 1, the instantaneous cell potential is equal to the standard cell potential.
When Q is greater than one, the instantaneous cell potential is less than the standard cell potential.
When Q is less than one, the instantaneous cell potential is greater than the standard cell potential.
When Q is equal to the equilibrium constant K, the instantaneous cell potential is equal to zero volts.
When Q is equal to K and the potential is equal to zero, the reaction is at equilibrium. However, for these first three situations, Q is not equal to K, and the instantaneous cell voltage is not equal to zero; therefore, the reaction is not at equilibrium.