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Chemistry · Simulation and virtual lab Free

Electrochemical cells: electrode potentials, salt bridge and the Nernst equation

Build cells from magnesium, zinc, iron, lead, copper and silver, read the voltage and see which way the electrons flow.

  • Best for S6 · Unit 11: Electrochemical cells and applications
  • Also useful S4 · Unit 16: Reduction and oxidation reactions (oxidation and reduction half-equations)
  • Also useful S5 · Unit 13: Electrolysis (cells that use and cells that make electricity)
You will learn to
  • Measure cell voltages and identify the anode, the cathode and the direction of electron flow.
  • Calculate E°cell from standard electrode potentials and write the cell reaction.
  • Explain the role of the salt bridge and the effect of concentration (Nernst equation).
You will measure
Voltage of each cell (V), at different concentrations.
Time needed
About 30–40 min
Equipment
Nothing extra. Real version: metal strips, 1 M metal salt solutions, beakers, filter-paper salt bridge soaked in KNO₃, high-resistance voltmeter, leads.
Price
Free: no payment, no account.

Simulation

Torch batteries, the lead–acid battery of a moto and the corrosion of iron roofing sheets all come from the same idea: two metals with different tendencies to lose electrons. Connecting them through a wire and a salt bridge gives a voltage that you can predict from standard electrode potentials.

Change and observe

Virtual lab

Follow the steps with the simulation above (go back to the simulation ↑). Each time you tap Record, a row is added to the table and a point to the graph.

Aim

To measure the voltage of electrochemical cells made from different metals, to identify the anode and cathode, to relate the cell voltage to standard electrode potentials, and to investigate the effect of concentration (Nernst equation).

What to do

  1. Build Zn | Zn²⁺ || Cu²⁺ | Cu with 1 M solutions. Read the voltage and record. Which metal is the anode?
  2. Write the two half-equations shown. In which direction do the electrons flow in the wire?
  3. Remove the salt bridge. What happens to the reading? Explain.
  4. Try Mg | Cu, Fe | Cu and Zn | Ag. Compare each reading with E°(right) − E°(left).
  5. Swap the electrodes (put Cu on the left). What happens to the sign of the reading?
  6. Keep Zn | Cu and change the copper(II) concentration to 0.1, 0.01 and 0.001 M. Record and look at the graph.

Results

Questions

What is the function of the salt bridge?

It completes the circuit by letting ions move between the two solutions, keeping each solution electrically neutral, without mixing them.

Which electrode is the anode in a Zn–Cu cell, and what happens there?

Zinc is the anode (negative electrode): oxidation, Zn → Zn²⁺ + 2e⁻.

Calculate E°cell for Zn | Zn²⁺ || Cu²⁺ | Cu. (E°: Zn −0.76 V, Cu +0.34 V)

E°cell = E°(cathode) − E°(anode) = 0.34 − (−0.76) = +1.10 V.

Why does a Mg–Ag cell give a larger voltage than a Fe–Cu cell?

Magnesium and silver are much further apart in the electrochemical series (E° −2.37 V and +0.80 V, a difference of 3.17 V) than iron and copper (0.78 V).

What does a negative voltmeter reading mean in this simulation?

The voltmeter is connected the other way round: the left electrode is the positive one (cathode).

What happens to the voltage of a Zn–Cu cell when the Cu²⁺ concentration is reduced?

It falls, because the reduction Cu²⁺ + 2e⁻ → Cu becomes less favourable (about 30 mV less for each tenfold dilution).

For teachers: expected results and how the model works

Electrode potentials used (V, 298 K): Mg²⁺/Mg −2.37, Zn²⁺/Zn −0.76, Fe²⁺/Fe −0.44, Pb²⁺/Pb −0.13, Cu²⁺/Cu +0.34, Ag⁺/Ag +0.80. Each electrode potential is E = E° + (0.0592 ÷ n) log[ion]; the voltmeter reads E(right) − E(left) with an ideal high-resistance voltmeter (no current drawn), so a negative reading means the left electrode is positive. Check values with 1 M solutions: Zn–Cu 1.100 V, Mg–Ag 3.170 V, Fe–Cu 0.780 V, Pb–Ag 0.930 V. Zn–Cu with 0.01 M Cu²⁺: 1.041 V. Two identical electrodes at different concentrations give a concentration cell (e.g. Cu 1 M and Cu 0.001 M: 0.089 V). Removing the salt bridge gives 0 V. Real cells give slightly lower readings because of internal resistance and oxide layers.

Exam practice Exam set

National-exam style questions on this simulation (15 marks). Try each one on paper first, then open the marking scheme.

A cell is made from Fe | Fe²⁺ (1 M) and Ag⁺ (1 M) | Ag. E°: Fe²⁺/Fe −0.44 V, Ag⁺/Ag +0.80 V. (a) Write the cell diagram. (b) Calculate E°cell. (c) Write the overall equation. (6 marks)

Marking scheme: (a) Fe(s) | Fe²⁺(aq) || Ag⁺(aq) | Ag(s) (2). (b) 0.80 − (−0.44) = +1.24 V (2). (c) Fe + 2Ag⁺ → Fe²⁺ + 2Ag (2).

Use the Nernst equation E = E° − (0.0592 ÷ n) log Q to find the voltage of Zn | Zn²⁺ (1.0 M) || Cu²⁺ (0.010 M) | Cu. (E° = 1.10 V) (4 marks)

Marking scheme: Zn + Cu²⁺ → Zn²⁺ + Cu, n = 2 (1); Q = [Zn²⁺] ÷ [Cu²⁺] = 1.0 ÷ 0.010 = 100 (1); E = 1.10 − 0.0296 × 2 (1) = 1.04 V (1).

Explain, using electrode potentials, why iron roofing sheets are coated with zinc (galvanised). (3 marks)

Marking scheme: Zinc has a more negative electrode potential than iron (1), so zinc is oxidised in preference to iron (1), protecting the iron even if the coating is scratched (sacrificial protection) (1).

State two conditions that must be met for the voltage of a cell to equal E°cell. (2 marks)

Marking scheme: Solutions of concentration 1 mol/dm³ (1); temperature 298 K and gases at 100 kPa / no current drawn (1).

For class and homework

The worksheet has the steps, an empty results table, a graph grid and all the questions with answer lines. The marking scheme has the expected results and every answer with its marks.