Curriculum
- 12 Sections
- 69 Lessons
- 100 Hours
- Chapter 1 (Solid State)4
- Chapter 2 (Solutions)10
- 2.0Types of solutions20 Minutes
- 2.1Ways of expressing concentrations 120 Minutes
- 2.2Ways of expressing concentrations 220 Minutes
- 2.3Henry’s Law and applications 120 Minutes
- 2.4Raoult’s Law and applications 220 Minutes
- 2.5Colligative property 110 Minutes
- 2.6Colligative property 215 Minutes
- 2.7Colligative property 315 Minutes
- 2.8Colligative property 415 Minutes
- 2.9Abnormal Molecular Mass15 Minutes
- Chapter 3 (Electro Chemistry)8
- 3.1Electrolytic conductivity 120 Minutes
- 3.2Debye Huckel limiting law15 Minutes
- 3.3Electrochemical Cell20 Minutes
- 3.4Cell potential in electrochemistry20 Minutes
- 3.5How to use Nernst equation20 Minutes
- 3.6Gibbs free energy in electrochemistry20 Minutes
- 3.7Understand Faradays Laws of Electrolysis20 Minutes
- 3.8Fundamentals of commercial batteries20 Minutes
- Chapter 4 (Chemical Kinetics)6
- 4.1How to calculate rate of reaction20 Minutes
- 4.2How to calculate reaction law and orders20 Minutes
- 4.3Initial rate method know it all faster15 Minutes
- 4.4How to use integral method in kinetics 120 Minutes
- 4.5How to use integral method in kinetics 215 Minutes
- 4.6How Collision Theory Explains Chemical Reactions20 Minutes
- Chapter 8 (d-block Elements)7
- 5.1d block electron configuration charts10 Minutes
- 5.2Trend across d block 1 atomic radii10 Minutes
- 5.3Trend across d block 2 melting point10 Minutes
- 5.4Trend across d block 3 Ionization energy10 Minutes
- 5.5Trend across d block 4 Oxidation state10 Minutes
- 5.6Trend in d block 5 Electrode Potential10 Minutes
- 5.7Trend in d block metal properties
- Chapter 9 (Co-ordinate Compounds)6
- Chapter 10 (Haloalkanes Haloarenes)7
- Chapter 11 (Alcohols, Phenols Ethers)7
- Chapter 12 (Aldehyde Ketones)4
- Chapter 12 (Carboxylic acid, Derivatives)3
- Chapter 13 (Amines)3
- Chapter 14 (Biomolecules)4
Gibbs free energy in electrochemistry
Gibbs free energy in electrochemistry
Table of Contents

Introduction
Understanding the intricate of Gibbs free energy in electrochemistry, relationship between Gibbs free energy, electromotive force (EMF) of a cell, and the equilibrium constant is fundamental for anyone delving into the world of electrochemistry.
As you explore how these concepts interconnect, you’ll uncover the underlying principles that govern chemical reactions and energy changes in electrochemical cells.
This blog post will break down the significance of Gibbs free energy and its role in determining the spontaneity of reactions, while also clarifying how EMF serves as an indicator of a cell’s ability to perform work. We’ll also delve into the equilibrium constant, shedding light on how it reflects the balance between reactants and products at equilibrium.
Join us as we navigate this complex yet fascinating topic, providing you with insights that will enhance your understanding of electrochemical processes and their applications in real-world scenarios.
The Relationship Between Gibbs Free Energy and EMF
Understanding Gibbs free energy in electrochemistry, the relationship between Gibbs free energy and the electromotive force (EMF) of a cell is crucial in the field of electrochemistry, as it helps elucidate the spontaneity of electrochemical reactions. At its core, Gibbs free energy (G) measures the maximum reversible work obtainable from a thermodynamic system.
In electrochemistry, this concept is directly tied to the potential difference (Ecell) measured in volts between the electrodes of a galvanic cell, known as EMF. The fundamental equation that links Gibbs free energy (ΔG) to EMF (E) is given by:

This relationship indicates that a negative Gibbs free energy change corresponds to a positive EMF, signifying that the electrochemical reaction is spontaneous. Conversely, a positive Gibbs free energy change correlates with a negative EMF, indicating that the reaction is non-spontaneous.
Additionally, this relationship can be connected to the equilibrium constant (K) of the reaction through the following equation:

From these equations, we can derive that the relationship between Gibbs free energy, EMF, and the equilibrium constant is interlinked.
A large value of K (indicating that products are favored at equilibrium) results in a negative Gibbs free energy, and consequently, a positive EMF. In essence, a spontaneous reaction not only suggests that the system can perform work but also reflects on the balance between reactants and products as dictated by the equilibrium constant.
In practical applications, this understanding allows chemists and engineers to assess and predict the behavior of electrochemical cells under different conditions, facilitating the design of efficient energy storage and conversion systems, such as batteries and fuel cells