half-cell

(noun)

Either of the two parts of an electrochemical cell containing an electrode and an electrolyte.

Related Terms

  • voltaic cell
  • electrode
  • redox

Examples of half-cell in the following topics:

  • Electrochemical Cell Notation

    • Cell notation is shorthand that expresses a certain reaction in an electrochemical cell.
    • The anode half-cell is described first; the cathode half-cell follows.
    • Within a given half-cell, the reactants are specified first and the products last.
    • A double vertical line ( || ) represents a salt bridge or porous membrane separating the individual half-cells.
    • A typical arrangement of half-cells linked to form a galvanic cell.
  • Voltaic Cells

    • A voltaic cell is a device that produces an electric current from energy released by a spontaneous redox reaction in two half-cells.
    • This redox reaction consists of two half-reactions.
    • In a typical voltaic cell, the redox pair is copper and zinc, represented in the following half-cell reactions:
    • Each half-cell is connected by a salt bridge, which allows for the free transport of ionic species between the two cells.
    • The cell consists of two half-cells connected via a salt bridge or permeable membrane.
  • Predicting if a Metal Will Dissolve in Acid

    • Each half-cell is associated with a potential difference whose magnitude depends on the nature of the particular electrode reaction and on the concentrations of the dissolved species.
    • In order to express them in a uniform way, we follow the rule that half-cell potentials are always defined for the reduction direction.
    • Therefore, the half-cell potential for the Zn/Zn2+ electrode always refers to the reduction reaction:
    • For this reason, the potential difference contributed by the left half-cell has the opposite sign to its conventional reduction half-cell potential.
    • Set up the oxidation and reduction half-reactions with their cell potential:
  • Concentration of Cells

    • The standard potential of an electrochemical cell requires standard conditions for all of the reactants.
    • The change in Gibbs free energy for an electrochemical cell can be related to the cell potential.
    • The Nernst equation can be used to calculate the output voltage changes in a pair of half-cells under non-standard conditions.
    • Under standard conditions, the output of this pair of half-cells is well known.
    • Discuss the implications of the Nernst equation on the electrochemical potential of a cell
  • The Nernst Equation

    • In electrochemistry, the Nernst equation can be used to determine the reduction potential of an electrochemical cell.
    • In electrochemistry, the Nernst equation can be used, in conjunction with other information, to determine the reduction potential of a half-cell in an electrochemical cell.
    • Find the cell potential of a galvanic cell based on the following reduction half-reactions where [Ni2+] = 0.030 M and [Pb2+] = 0.300 M.
    • First, find the electromotive force for the standard cell, which assumes concentrations of 1 M.
    • The added half-reactions with the adjusted E0 cell are:
  • Free Energy and Cell Potential

    • The basis for an electrochemical cell, such as the galvanic cell, is always a redox reaction that can be broken down into two half-reactions: oxidation occurs at the anode, where there is a loss of electrons, and reduction occurs at the cathode, where there is a gain of electrons.
    • If E°cell > 0, then the process is spontaneous (galvanic cell)
    • If E°cell < 0, then the process is non-spontaneous (the voltage must be supplied, as in an electrolytic cell)
    • A demonstration electrochemical cell setup resembling the Daniell cell.
    • The two half-cells are linked by a salt bridge carrying ions between them.
  • Equilibrium Constant and Cell Potential

    • In electrochemistry, the Nernst equation can be used, in conjunction with other information, to determine the equilibrium reduction potential of a half-cell.
    • For example, let's say a concentration gradient was established by dissolving KCl in half of a divided vessel that was originally full of H2O.
    • In order to calculate the standard potential, we have to look up the half-reactions of copper and zinc.
    • The cell equilibrium constant, K, can be derived from the Nernst equation:
    • Schematic of a galvanic cell for the reaction between Zn and Cu.
  • Dry Cell Battery

    • The dry cell is one of many general types of electrochemical cells.
    • Unlike a wet cell, a dry cell can operate in any orientation without spilling, as it contains no free liquid.
    • A common dry-cell battery is the zinc-carbon battery, which uses a cell that is sometimes called the Leclanché cell.
    • The paste of ammonium chloride reacts according to the following half-reaction:
    • An illustration of a zinc-carbon dry cell.
  • Predicting Spontaneous Direction of a Redox Reaction

    • This means that Li would be written as the reduction half-reaction when compared to any other element in this table.
    • On the other hand, Fe would be written as the oxidation half-reaction when compared to any other element on this table.
    • For example if we turn the zinc oxidation half-reaction around ($Zn^{2+} + 2e^- \rightarrow Zn \ E^o = -0.76 V$), the cell potential is reversed.
    • The relative reactivities of different half-reactions can be compared to predict the direction of electron flow.
    • Predict the direction of electron flow in a redox reaction given the reduction potentials of the two half-reactions
  • Phospholipids

    • Phospholipids are the main constituents of cell membranes.
    • The phospholipid molecules can move about in their half the bilayer, but there is a significant energy barrier preventing migration to the other side of the bilayer.
    • A cell may be considered a very complex liposome.
    • The interior of a cell contains a variety of structures (organelles) that conduct chemical operations vital to the cells existence.
    • Molecules bonded to the surfaces of cells serve to identify specific cells and facilitate interaction with external chemical entities.
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