Detailed Summary
Electrochemical cells are crucial in the field of chemistry for their role in converting chemical energy into electrical energy and vice versa. This section introduces the fundamental concepts of electrochemical cells, detailing the two main types:
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Galvanic Cells: These cells convert spontaneous chemical reactions into electrical energy. A common example is the Daniell cell which operates through redox reactions, specifically the oxidation of zinc (Zn) and the reduction of copper ions (Cu2+). The electrical potential generated by a galvanic cell is measured as cell potential or electromotive force (emf) and can be calculated using the standard electrode potentials of the involved half-reactions.
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Electrolytic Cells: In contrast to galvanic cells, electrolytic cells require an external electrical input to drive non-spontaneous reactions. When an opposite potential is applied to a galvanic cell, it functions as an electrolytic cell, reversing the flow of current and enabling chemical reactions that would not occur on their own.
The Nernst equation is introduced to calculate the emf of galvanic cells based on reaction conditions, showcasing its dependence on temperature and concentration of reacting species. Additionally, the section discusses the concepts of conductivity and molar conductivity of solutions, emphasizing their importance in predicting how well ions can conduct electricity in different concentrations. Key principles such as Kohlrausch's law are highlighted, helping to understand how limiting molar conductivities are derived from individual ions based on their migration.
Final reflections in this section stress the significance of studying electrochemical cells for both theoretical and practical applications, including battery technology, electrolysis processes, and environmental implications related to energy efficiency.