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ELECTROCHEMISTRY CHM578
LABORATORY REPORT
EXPERIMENT 1 : GALVANIC CELL
INTRODUCTION
In any electrochemical process, electrons flow from one chemical substance to
another, driven by an oxidation–reduction (redox) reaction. A redox reaction occurs when
electrons are transferred from a substance that is oxidized to one that is being reduced.
The reductant is the substance that loses electrons and is oxidized in the process;
the oxidant is the species that gains electrons and is reduced in the process. The associated
potential energy is determined by the potential difference between the valence electrons in
atoms of different elements. The fundamental measurement in electrochemistry is the
voltage (V) of an electrochemical cell. The voltage describes the relative energies of
electrons on different atoms and/or ions. The potential difference between two electrons is
measured in volts(joules/coulomb). The electrons can be on two ends of a wire, on two
atoms or on the cathode and anode of a battery having a potential difference. An oxidation-
reduction or redox reaction is a chemical reaction in which one or more electrons from one
molecule or atom are transferred to another. Thermodynamics can predict if electrons
would prefer to be transferred from one species to another based on the free energy
change of the system. An electrochemical cell is produced when a redox reaction occurs.
The resulting electron transfer between the reactions runs through an external wire. The
oxidation and reduction reactions are physically separated from each other, so they are
called half-cell reactions. A half-cell can be prepared with most any metal in contact with a
solution of its ions. Each element own unique electron configuration means that each
element has a different electrical potential, so different combinations of oxidation and
reduction half-cells result in different voltages for the completed electrochemical cell.
Moreover, the main function of the Nernst equation is to calculate the ion's equilibrium
potential at a given concentration gradient. The equilibrium potential is the theoretical
intracellular electrical potential that would be equal in magnitude but opposite in direction
to the concentration force. Electric work done by a galvanic cell is mainly due to the Gibbs
energy of spontaneous redox reaction in the voltaic cell. It generally consists of two half
cells and a salt bridge. Each half cell further consists of a metallic electrode dipped into an
electrolyte. These two half-cells are connected to a voltmeter and a switch externally with
the help of metallic wires. In some cases, when both the electrodes are dipped in the same
electrolyte, a salt bridge is not required.
APPARATUS
Beaker
Voltmeter
Sand paper or steel wool
Electrical wire
Crocodile clips
Filter paper
100 ml Volumetric flask
pipet
CHEMICALS
Deionized water
strips of copper, zinc, and ion metals
1.1 M solutions
Zn(NO3)2 solution
1M CuSO4
0.001M CuSO4
5mL of 6M NH3
PROCEDURE
Four small beakers was obtained and 0.1 M solutions filled them. These solution
was share with other groups of students in the laboratory.
Strips of copper, zinc and iron metal was polish with emery/sand paper or steel
wool, rinse briefly with deionized water.
These polished metals was used as electrodes and put in their respective beaker.
Potentiometer (voltmeter) was check out with attached the two electrical wire
( different colour ) to crocodile clips.
A Cu strips (electrode) was placed in the Cu¿ ¿ solution and a Zn strip (electrode)
in the Zn( NO 3 ¿2 solution. A piece of filter paper was roll and flatten; the filter
paper was wet with a 0.1M KNO3 solution. The filter paper was fold and insert
the ends into solutions in the two beakers, this is the salt bridge. One electrode
was connect to the negative terminal of the potentiometer and other to the
positive terminal.
The cell potentials was determined for all possible galvanic cells that can be
constructed from the other redox couples. A ‘new’ salt bridge was prepared for
the each galvanic cell.
PROCEDURE
The galvanic cells was set up, 1 M Cu SO 4 and 0.001 M Cu sO4 solutions.
A polished copper electrode was immersed in each solution. a salt bridge
was prepared to connect the two redox couples. The cell potentials was
measured, the anode and cathode was determine. Write an equation for the
reaction occurring at each electrode.
Solution 1 was prepared through 4 as outline 1 mL pipet was used and 100
ml volumetric flasks. Before making the transfer, rinse the pipet with the
more concentrated solution. Deionized water was used for dilution to the
mark in the volumetric flasks. Calculate the molar concentration of each
solution.
2. Measure and Calculate the cell potentials for Solution 4.
The experiment was set up using small beaker. The Zn2+¿¿/ Zn redox couple
was the reference half-cell for this part of the experiment. The two half-cells
was connected with a new salt bridge. The electrodes was connected to the
potentiometer and was recorded the potentials difference, Ecell . Calculate
the theoretical cell potentials.
3. Measure and Calculate the Cell Potentials for the Solution 3 and 2.
Plot Ecell (measured ) and Ecell (calculated ) versus log [Cu2+¿ ¿] on the graph paper for
the four concentrations of Cu( NO 3 ¿2.
Calculation
Q = [Product]
[Reactant]
= [0.10]
[0.10]
=1
Ecell = EoCell – RT ln Q
nF
= [(0.34V) - (-0.79V)] - (8.314 JK-1mol-1 x 298K) ln (1)
2 mol x 96500 Cmol-1
= 1.13 V
% Error = 1.13V - 0.95V x 100
1.13V
= 15.93 %
Q = [Product]
[Reactant]
= [0.10]
[0.10]
=1
Ecell = EoCell – RT ln Q
nF
= [(0.34V) - (-0.45V)] - (8.314 JK-1mol-1 x 298K) ln (1)
2 mol x 96500 Cmol-1
= 0.79 V
Q = [Product]
[Reactant]
= [0.10]
[0.10]
=1
Ecell = EoCell – RT ln Q
nF
= [(-0.45) - (-0.79V)] - (8.314 JK-1mol-1 x 298K) ln (1)
2 mol x 96500 Cmol-1
= 0.34 V
A light blue solution is formed at 0.001 M CuSO 4 solution half-cell. Adding ammonia solution
causes the complex [Cu(NH 3)4]2+ to form in the cathode half-cell. (0.001M solution). This
therefore changes the potential of the cell. As the concentration of Cu 2+ ions in the half-cell
decreases, the overall cell potential will increase. This is due to the increasingly widening
gap between concentrations of the two half-cell solutions.
3. How would the cell potential have been affected if the NH 3 (aq) had been added to the
1 M CuSO4 solution instead of the 0.0010 M CuSO4 solution of the cell? Explain.
The potential changes as concentration of the solution decreases. NH 3 is used to reduce the
Cu2+ into a complex ion, therefore decreases the ionic Cu concentration and create potential
differences.
C: The Nernst Equation and an Unknown Concentration
Calculation
1st solution
Q = [Zn2+]
[Cu2+]
= [0.10]
[0.10]
=1
Ecell = EoCell – RT ln Q
nF
= [(0.34V) - (-0.79V)] - (8.314 JK-1mol-1 x 298K) ln (1)
2 mol x 96500 Cmol-1
= 1.13 V
2nd solution
Q = [Zn2+]
[Cu2+]
= [0.10]
[0.001]
= 100
Ecell = EoCell – RT ln Q
nF
= 1.13V - (8.314 JK-1mol-1 x 298K) ln (100)
2 mol x 96500 Cmol-1
= 1.07V
3rd Solution
Q = [Zn2+]
[Cu2+]
= [0.10]
[0.0001]
= 1000
Ecell = EoCell – RT ln Q
nF
= 1.13V - (8.314 JK-1mol-1 x 298K) ln (1000)
2 mol x 96500 Cmol-1
= 1.04V
4th solution
Q = [Zn2+]
[Cu2+]
= __[0.10]___
[0.0000001]
= 100
Ecell = EoCell – RT ln Q
nF
= 1.13V - (8.314 JK-1mol-1 x 298K) ln (1000000)
2 mol x 96500 Cmol-1
= 0.95V
GRAPHS
2. Ecell for the solution of unknown concentration: 0.05V
Molar concentration of Cu2+ in unknown (based on graph): Log [Cu2+] unknown is -1.5.
Therefore, 10(-1.5) = 0.032M
3. How would you adjust the concentrations of Cu 2+ and Zn2+ for the Cu-Zn cell to
maximize the cell potential? Explain.
The concentration Zn(NO 3)2 needs to be decrease while the concentration of Cu(NO 3)2
needs to decrease. This will give a lower value of Q and based on Nernst value the decrease
the Q will increase the E cell (V).
Discussion
From the first table at the results section shows that the reduction potential (measured) is
compared with the standard reduction potential (calculated). The measured reduction
potential for the three redox couple was arranged in in order of decreasing (measured)
reduction potentials. For the Cu-Zn the measured reduction potential was the higher among
the other couples. The errors had occurred during the experiment was conducted. The error
maybe is cause by connection of circuit that not connected properly during the experiment
and the apparatus that being used was broke. For the precaution step must be followed is
to be ensure the connection is connected properly. Another error is about polished the
electrodes. Electrodes must be polished to avoid any impurities that can cause the
connection of electricity. After polished the electrodes are rinsed with distilled water
because to remove any coated element that still on the electrodes
REFERENCES
1. https://www.saddleback.edu/faculty/cabel/Saddleback/Chem_1B_Schedule_files/Ex
p18-electrochem-lab-sp20.pdf
2. https://opentextbc.ca/chemistry/chapter/17-2-galvanic-cells/
3. https://byjus.com/chemistry/galvanic-cell/