Voltaic Cells
A Voltaic Cell (also known as a Galvanic Cell) is an electrochemical cell that uses spontaneous redox reactions to generate electricity. It consists of two separate half-cells. A half-cell is composed of an electrode (a strip of metal, M) within a solution containing Mn+
ions in which M is any arbitrary metal. The two half cells are linked
together by a wire running from one electrode to the other. A salt
bridge also connects to the half cells. The functions of these parts are
discussed below.
Half Cells
Half of the redox reaction occurs at each half cell. Therefore, we can say that in each half-cell a half-reaction is taking place. When the two halves are linked together with a wire and a salt bridge, an electrochemical cell is created.Electrodes
An electrode is strip of metal on which the reaction takes place. In a voltaic cell, the oxidation and reduction of metals occurs at the electrodes. There are two electrodes in a voltaic cell, one in each half-cell. The cathode is where reduction takes place and oxidation takes place at the anode. The figures below illustrate a cathode and an anode.
Through electrochemistry, these reactions are reacting upon metal surfaces, or electrodes. An
oxidation-reduction equilibrium is established between the metal and
the substances in solution. When electrodes are immersed in a solution
containing ions of the same metal, it is called a half-cell.
Electrolytes are ions in solution, usually fluid, that conducts
electricity through ionic conduction. Two possible interactions can
occur between the metal atoms on the electrode and the ion solutions.
- Metal ion Mn+ from the solution may collide with the electrode, gaining "n" electrons from it, and convert to metal atoms. This means that the ions are reduced.
- Metal atom on the surface may lose "n" electrons to the electrode and enter the solution as the ion Mn+ meaning that the metal atoms are oxidized.
Anode
The
anode is where the oxidation reaction takes place. In other words, this
is where the metal loses electrons. In the reaction above, the anode is
the Ag(s) since it increases in oxidation state from 0 to +1.
Cathode
The cathode is where the reduction
reaction takes place. This is where the metal electrode gains electrons.
Referring back to the equation above, the cathode is the Cu(s) as it
decreases in oxidation state from +2 to 0.
Remembering Oxidation and Reduction
When it comes to redox reactions, it is
important to understand what it means for a metal to be “oxidized” or
“reduced”. An easy way to do this is to remember the phrase “OIL RIG”.
OIL = Oxidization is Loss (of e-)
RIG = Reduction is Gain (of e-)
In the case of the example above Ag+(aq) gains an electron meaning it is reduced. Cu(s) loses two electrons thus it is oxidized.
Salt Bridge
The salt bridge is a vital component of any voltaic cell. It is a tube filled with an electrolyte solution such as KNO3(s) or KCl(s). The purpose of the salt bridge is to keep the solutions electrically neutral and allow the free flow of ions from one cell to another. Without the salt bridge, positive and negative charges will build up around the electrodes causing the reaction to stop.Flow of Electrons
Electrons always flow from the anode to the cathode or from the oxidation half cell to the reduction half cell. In terms of Eocell of the half reactions, the electrons will flow from the more negative half reaction to the more positive half reaction.
Cell Diagram
A cell diagram is a representation of an electrochemical cell. The figure below illustrates a cell diagram for the voltaic shown in Figure 1 above.
Figure 2 Cell Diagram
When drawing a cell diagram, we follow the following conventions. The anode is always placed on the left side, and the cathode is placed on the right side. The salt bridge is represented by double vertical lines (||). The
difference in the phase of an element is represented by a single
vertical line (|), while changes in oxidation states are represented by
commas (,).
Constructing a Cell Diagram
When asked to construct a cell diagram follow these simple instructions.Consider the following reaction:
2Ag+(aq) + Cu(s) ↔ Cu2+(aq) + 2Ag(s)
Step 1: Write the two half-reactions.
Ag+(aq) + e- ↔ Ag(s)
Cu(s) ↔ Cu2+(aq) + 2e-
Step 2: Determine the cathode and anode.
Anode: Cu(s) ↔ Cu2+(aq) + 2e-
Cathode: Ag+(aq) + e- ↔ Ag(s)
Cu(s) is losing electrons thus being oxidized. Oxidation happens at the anode. Ag+ is gaining electrons thus is being reduced. Reduction happens at the cathode.Step 3: Construct the Diagram.
Cu(s) | Cu2+(aq) || Ag+(aq) | Ag(s)
The anode always goes on the left and
cathode on the right. Separate changes in phase by | and indicate the
the salt bridge with ||.
Cell Voltage/Cell Potential
The readings from the voltmeter give the reaction's cell voltage or potential difference between it's two two half-cells. Cell voltage is also known as cell potential or electromotive force (emf) and it is shown as the symbol Ecell.
Standard Cell Potential: Eocell = Eoright(cathode) - Eoleft(anode)
The Eo values are tabulated with all solutes at 1 M and all gases at 1 atm. These values are called standard reduction potentials.
Each half-reaction has a different reduction potential, the difference
of two reduction potentials gives the voltage of the electrochemical cell. If Eocell is positive the reaction is spontaneous and it is a voltaic cell. If the Eocell is negative, the reaction is non-spontaneous and it is referred to as an electrolytic cell.
This is a link that shows the standard reduction potentials of all common half-reactions: http://butane.chem.uiuc.edu/cyerkes/.../standpot.html
Practice Problems
Consider the following two reactions:
a) Cu2+(aq) + Ba(s) --> Cu(s) + Ba2+(aq)
b) Al(s) + Sn2+(aq) --> Al3+(aq) + Sn(s)
1. Split the reaction into half reactions and determine their Eo value. Indicate which would be the anode and cathode.
2. Construct a cell diagram for the following each reactions.
3. Determine the Eocell for the voltaic cell formed by each reaction.
*Solution are given below.
Solutions
1.a) Ba2+(aq) + 2e- --> Ba(s) Eo = -2.92 V Anode
Cu2+(aq) + 2e- --> Cu(s) Eo = +0.340 V Cathode
1.b) Al3+(aq) 3e- --> Al(s) Eo = -1.66 V Anode
Sn2+(aq) --> Sn(s) +2e- Eo = -0.137 V Cathode
2.a) Ba2+(aq) | Ba(s) || Cu(s) | Cu2+(aq)
2.b) Al(s) | Al3+(aq) || Sn2+(aq) | Sn(s)
3.a) Eocell = 0.34 - (-2.92) = 3.26 V
3.b) Eocell = -0.137 - (-1.66) = 1.523 V
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