Table of Contents
ToggleElectrochemical cells generate electrical energy through chemical reactions. However, these reactions don’t always occur under standard conditions (298.15 K, 1 atm, and 1 M concentrations). Understanding how cell potential varies under nonstandard conditions is crucial for predicting and analyzing cell performance in real-world scenarios. In this section, we’ll explore how concentration, cell potential, and equilibrium interplay using the Nernst Equation.
Recall from earlier lessons that standard cell potential (E°cell) is calculated when all components are under standard conditions. However, real electrochemical cells often operate under nonstandard conditions. The potential under these conditions, denoted as Ecell, can differ from E°cell based on the concentrations of reactants and products.
Key Insight: A galvanic cell that is actively running is not at equilibrium. As the cell moves toward equilibrium, its potential decreases until it eventually reaches zero—similar to a dead battery.
As a cell approaches equilibrium:
The Nernst Equation quantifies the relationship between Ecell and E°cell under nonstandard conditions:
Where:
Key Takeaway: The Nernst Equation allows us to predict how the cell potential will change based on the concentrations of the reactants and products.
Concentration plays a pivotal role in determining Ecell:
Example Calculation: Consider the reaction:
We analyze how different conditions affect Ecell compared to E°cell:
Tip: A higher product concentration (Q > 1) leads to a decrease in cell potential, while a higher reactant concentration (Q < 1) increases it.
The Nernst Equation is a powerful tool for predicting how changes in concentration, temperature, and reaction conditions affect cell potential. While you won’t be required to perform complex calculations on the AP Chemistry Exam, understanding the qualitative relationships between E°cell, Ecell, and Q is essential.
Given:
Calculate the effect of different concentrations on Ecell using the Nernst Equation:
Remember that cell potential directly relates to the spontaneity of a reaction through Gibbs Free Energy (ΔG):
This relationship underscores how changes in Ecell can affect the overall energy and feasibility of reactions.