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Chapter 20: Electrochemistry

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1 Chapter 20: Electrochemistry
Chemistry 140 Fall 2002 General Chemistry Principles and Modern Applications Petrucci • Harwood • Herring 10th Edition Chapter 20: Electrochemistry Mamdouh Abdelsalam King Faisal University Prentice-Hall © 2002

2 General Chemistry: Chapter 21
Chemistry 140 Fall 2002 Contents 20-1 Electrode Potentials and Their Measurement 20-2 Standard Electrode Potentials 20-3 Ecell, ΔG, and Keq 20-4 Ecell as a Function of Concentration 20-5 Batteries: Producing Electricity Through Chemical Reactions. 20-6 Corrosion: Unwanted Voltaic Cells 20-7 Electrolysis: Causing Non-spontaneous Reactions to Occur 20-8 Industrial Electolysis Processes Focus On Membrane Potentials Prentice-Hall © 2002 General Chemistry: Chapter 21

3 20-1 Electrode Potentials and Their Measurement
Cu(s) + 2Ag+(aq) Cu2+(aq) + 2 Ag(s) Cu(s) + Zn2+(aq) No reaction Prentice-Hall © 2002 General Chemistry: Chapter 20

4 An Electrochemical Half Cell
Anode Cathode Prentice-Hall © 2002 General Chemistry: Chapter 20

5 An Electrochemical Cell
Chemistry 140 Fall 2002 An Electrochemical Cell Cu ⇢ Cu2+ + 2e- 2Ag+ + 2e-⇢ 2Ag Anode: oxidation Cathode: Reduction Section 1 Sunday Prentice-Hall © 2002 General Chemistry: Chapter 20

6 General Chemistry: Chapter 21
Salt bridge Salt bridge: To provide ions to the solution to keep the electro neutrality Prentice-Hall © 2002 General Chemistry: Chapter 21

7 General Chemistry: Chapter 20
Terminology Electromotive force, Ecell. The cell voltage or cell potential. Cell diagram. Shows the components of the cell in a symbolic way. Anode (where oxidation occurs) on the left. Cathode (where reduction occurs) on the right. Oil (oxidation is loss), Rig (Reduction is gaining) Boundary between phases shown by |. Boundary between half cells (usually a salt bridge) shown by ||. Prentice-Hall © 2002 General Chemistry: Chapter 20

8 General Chemistry: Chapter 20
Terminology Zn ⇢Zn2+ + 2e- Cu2+ + 2e- ⇢Cu Zn(s) | Zn2+(aq) || Cu2+(aq) | Cu(s) Ecell = V Prentice-Hall © 2002 General Chemistry: Chapter 20

9 General Chemistry: Chapter 20
Terminology Galvanic cells. Convert chemical energy to electricity as a result of spontaneous reactions. Electrolytic cells. Convert electricity into chemical energy Non-spontaneous chemical change driven by electricity. Couple, M|Mn+ A pair of species related by a change in number of e-. Prentice-Hall © 2002 General Chemistry: Chapter 20

10 20-2 Standard Electrode Potentials
Cell voltages, the potential differences between electrodes, are among the most precise scientific measurements. The potential of an individual electrode is difficult to establish. Arbitrary zero is chosen. The Standard Hydrogen Electrode (SHE) Prentice-Hall © 2002 General Chemistry: Chapter 20

11 Standard Hydrogen Electrode
Chemistry 140 Fall 2002 Standard Hydrogen Electrode 2 H+(a = 1) + 2 e- ⇄ H2(g, 1 bar) E° = 0 V Pt|H2(g, 1 bar)|H+(a = 1) The two vertical lines indicate three phases are present. For simplicity we usually assume that a = 1 at [H+] = 1 M and replace 1 bar by 1 atm. Prentice-Hall © 2002 General Chemistry: Chapter 20

12 Standard Electrode Potential, E°
Chemistry 140 Fall 2002 Standard Electrode Potential, E° E° defined by international agreement. The tendency for a reduction process to occur at an electrode. All ionic species present at a=1 (approximately 1 M). All gases are at 1 bar (approximately 1 atm). Where no metallic substance is indicated, the potential is established on an inert metallic electrode (ex. Pt). Tuesday 12/12/2017 Prentice-Hall © 2002 General Chemistry: Chapter 20

13 General Chemistry: Chapter 20
Reduction Couples Cu2+(1M) + 2 e- → Cu(s) E°Cu2+/Cu = ? Pt|H2(g, 1 bar)|H+(a = 1) || Cu2+(1 M)|Cu(s) E°cell = V anode cathode Standard cell potential: the potential difference of a cell formed from two standard electrodes. E°cell = E°cathode - E°anode Prentice-Hall © 2002 General Chemistry: Chapter 20

14 Standard Cell Potential
Chemistry 140 Fall 2002 Standard Cell Potential Pt|H2(g, 1 bar)|H+(a = 1) || Cu2+(1 M)|Cu(s) E°cell = V E°cell = E°cathode - E°anode E°cell = E°Cu2+/Cu - E°H+/H2 0.340 V = E°Cu2+/Cu - 0 V E°Cu2+/Cu = V Wednesday (13/12/2017) H2(g, 1 atm) + Cu2+(1 M) → H+(1 M) + Cu(s) E°cell = V Prentice-Hall © 2002 General Chemistry: Chapter 20

15 Measuring Standard Reduction Potential
Chemistry 140 Fall 2002 Measuring Standard Reduction Potential anode cathode cathode anode Prentice-Hall © 2002 General Chemistry: Chapter 20

16 Standard Reduction Potentials
Chemistry 140 Fall 2002 Standard Reduction Potentials Section 2 Prentice-Hall © 2002 General Chemistry: Chapter 20

17 General Chemistry: Chapter 20
Chemistry 140 Fall 2002 20-3 Ecell, ΔG, and Keq Cells do electrical work. Moving electric charge. Faraday constant, F = 96,485 C mol-1 elec = -nFE ΔG = -nFE ΔG° = -nFE° Thursday section 1 (14/12/2017) Prentice-Hall © 2002 General Chemistry: Chapter 20

18 General Chemistry: Chapter 20
Chemistry 140 Fall 2002 Spontaneous Change ΔG < 0 for spontaneous change. Therefore E°cell > 0 because ΔGcell = -nFE°cell E°cell > 0 Reaction proceeds spontaneously as written. E°cell = 0 Reaction is at equilibrium. E°cell < 0 Reaction proceeds in the reverse direction spontaneously. Prentice-Hall © 2002 General Chemistry: Chapter 20

19 The Behavior of Metals Toward Acids
M(s) → M2+(aq) + 2 e- E° = -E°M2+/M 2 H+(aq) + 2 e- → H2(g) E°H+/H2 = 0 V 2 H+(aq) + M(s) → H2(g) + M2+(aq) E°cell = E°H+/H2 - E°M2+/M = -E°M2+/M When E°M2+/M < 0, E°cell > 0. Therefore ΔG° < 0. Metals with negative reduction potentials react with acids Prentice-Hall © 2002 General Chemistry: Chapter 20

20 Relationship Between E°cell and Keq
Chemistry 140 Fall 2002 Relationship Between E°cell and Keq ΔG° = -RT ln Keq = -nFE°cell E°cell = nF RT ln Keq Section 1 Tuesday Prentice-Hall © 2002 General Chemistry: Chapter 20

21 General Chemistry: Chapter 20
Chemistry 140 Fall 2002 Summary of Thermodynamic, Equilibrium and Electrochemical Relationships. Prentice-Hall © 2002 General Chemistry: Chapter 20

22 20-4 Ecell as a Function of Concentration
ΔG = ΔG° -RT ln Q -nFEcell = -nFEcell° -RT ln Q Ecell = Ecell° ln Q nF RT Convert to log10 and calculate constants Ecell = Ecell° log Q n V The Nernst Equation: Prentice-Hall © 2002 General Chemistry: Chapter 20

23 General Chemistry: Chapter 20
Example 20-8 Applying the Nernst Equation for Determining Ecell. What is the value of Ecell for the voltaic cell pictured below and diagrammed as follows? Pt|Fe2+(0.10 M),Fe3+(0.20 M)||Ag+(1.0 M)|Ag(s) Prentice-Hall © 2002 General Chemistry: Chapter 20

24 General Chemistry: Chapter 20
Example 20-8 Ecell = Ecell° log Q n V Ecell = Ecell° log n V [Fe3+] [Fe2+] [Ag+] Ecell = V – V = V Pt|Fe2+(0.10 M),Fe3+(0.20 M)||Ag+(1.0 M)|Ag(s) Fe2+(aq) + Ag+(aq) → Fe3+(aq) + Ag (s) Prentice-Hall © 2002 General Chemistry: Chapter 20

25 20-5 Batteries: Producing Electricity Through Chemical Reactions
Primary Cells (or batteries). Cell reaction is not reversible. (not rechargeable) Secondary Cells. Cell reaction can be reversed by passing electricity through the cell (rechargeable). Flow Batteries and Fuel Cells. Materials pass through the battery which converts chemical energy to electric energy. Prentice-Hall © 2002 General Chemistry: Chapter 20

26 Lead-Acid (Storage) Battery
Chemistry 140 Fall 2002 Lead-Acid (Storage) Battery The most common secondary battery Section 1 Thursday Prentice-Hall © 2002 General Chemistry: Chapter 20

27 General Chemistry: Chapter 20
Lead-Acid Battery Reduction: PbO2(s) + 3 H+(aq) + HSO4-(aq) + 2 e- → PbSO4(s) + 2 H2O(l) Oxidation: Pb (s) + HSO4-(aq) → PbSO4(s) + H+(aq) + 2 e- PbO2(s) + Pb(s) + 2 H+(aq) + 2HSO4-(aq) → 2 PbSO4(s) + 2 H2O(l) E°cell = E°PbO2/PbSO4 - E°PbSO4/Pb = 1.74 V – (-0.28 V) = 2.02 V Prentice-Hall © 2002 General Chemistry: Chapter 20

28 General Chemistry: Chapter 20
Fuel Cells O2(g) + 2 H2O(l) + 4 e- → 4 OH-(aq) 2{H2(g) + 2 OH-(aq) → 2 H2O(l) + 2 e-} 2H2(g) + O2(g) → 2 H2O(l) E°cell = E°O2/OH- - E°H2O/H2 = V – ( V) = V  = ΔG°/ ΔH° = 0.83 Prentice-Hall © 2002 General Chemistry: Chapter 20

29 20-6 Corrosion: Unwanted Voltaic Cells
Chemistry 140 Fall 2002 20-6 Corrosion: Unwanted Voltaic Cells In neutral solution: O2(g) + 2 H2O(l) + 4 e- → 4 OH-(aq) EO2/OH- = V 2 Fe(s) → 2 Fe2+(aq) + 4 e- EFe/Fe2+ = V 2 Fe(s) + O2(g) + 2 H2O(l) → 2 Fe2+(aq) + 4 OH-(aq) Ecell = V In acidic solution: Cancelled sem 1 ( ) O2(g) + 4 H+(aq) + 4 e- → 4 H2O (aq) EO2/OH- = V Prentice-Hall © 2002 General Chemistry: Chapter 20

30 General Chemistry: Chapter 20
Corrosion Protection Prentice-Hall © 2002 General Chemistry: Chapter 20

31 General Chemistry: Chapter 20
Corrosion Protection Prentice-Hall © 2002 General Chemistry: Chapter 20

32 20-7 Electrolysis: Causing Non-spontaneous Reactions to Occur
Galvanic Cell: Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s) EO2/OH- = V Electolytic Cell: Zn2+(aq) + Cu(s) → Zn(s) + Cu2+(aq) EO2/OH- = V Prentice-Hall © 2002 General Chemistry: Chapter 20

33 Faraday’s law The amount of chemical change is proportional to the amount of current passed. m mass of substance M molar mass I current A T time for which the current passe (s) n number of electrons transferred F Faraday constant (96485 C mol-1) M Abdelsalam


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