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Electric energy Chemical energy Electrolysis Galvanic cell Chapter 8 Electrochemistry.

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Presentation on theme: "Electric energy Chemical energy Electrolysis Galvanic cell Chapter 8 Electrochemistry."— Presentation transcript:

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2 Electric energy Chemical energy Electrolysis Galvanic cell Chapter 8 Electrochemistry

3 Electrochemistry Study of chemical reactions that can produce electricity or use electricity to produce desired product. Study of interchange of chemical and electrical energy Electrochemical reaction always involves oxidation-reduction reactions – Electron transfer reactions – Electrons transferred from one substance to another Also called redox reactions 2

4 Galvanic Cells

5 The Daniell Cell Flow of Zn 2+ Flow of SO 4 2- Half-cell Half-cell reaction

6 5 Needed to complete circuit Tube filled with solution of an electrolyte – Salt composed of ions not involved in cell reaction – KNO 3 and KCl often used Porous plugs at each end of tube – Prevent solution from pouring out – Enable ions from salt bridge to migrate between half- cells to neutralize charges in cell compartments Anions always migrate toward anode Cations always migrate toward cathode Salt Bridge Salt bridge

7 Anode compartment Half-cell Half-reaction: Oxidation Cathode compartment Half-cell Half-reaction: Reduction Zn (s) → Zn 2+ (aq) +2e - Cu 2+ (aq) + 2e - → Cu (s) Cu 2+ (aq) + Zn (s) → Cu (s) + Zn 2+ (aq) total cell reaction 2e -

8 7 Cell Notation Cu (s) |Cu 2+ (aq) ||Ag + (aq) |Ag (s) Single slash = boundary between phases (solid electrode and aqueous solution of ions) Double slash represents salt bridge – Separates cell reactions In each half (half-cell) – Electrodes appear at outsides – Reaction electrolytes in inner section – Species in same state separated with ; – Concentrations shown in ( ) anodecathode anode electrode anode electrolyte cathode electrolyte cathode electrode Salt Bridge

9 8 Learning Check Write the standard cell notation for the following electrochemical cells: Fe (s) + Cd 2+ (aq)  Cd (s) + Fe 2+ (aq) Anode = ox = Fe (s) Cathode = red = Cd 2+ (aq) Fe (s) |Fe 2+ (aq) ||Cd 2+ (aq) |Cd (s) Al (s) + Au 3+ (aq)  Al 3+ (aq) + Au (s) Anode = ox = Al (s) Cathode = red = Au 3+ (aq) Al (s) |Al 3+ (aq) ||Au 3+ (aq) |Au (s)

10 Your Turn! Write the standard cell notation (Pt electrodes) for the following reaction: 2Mn 3+ (aq) + 2I - (aq) → Mn 2+ (aq) + I 2 (s) A. Pt(s)|Mn 3+ (aq); Mn 2+ (aq)||I - (aq)|I 2 (s)|Pt(s) B. Pt(s)|I - (aq)|I 2 (s)||Mn 3+ (aq); Mn 2+ (aq)|Pt(s) C. Mn 3+ (aq)|Pt(s); Mn 2+ (aq)||I - (aq)|I 2 (s)|Pt(s) D. Pt(s)|Mn 3+ (aq); I - (aq)||Mn 2+ (aq)|I 2 (s)|Pt(s) Oxidation reaction is on the right and reduction reaction is on the left of the salt bridge (||). 9

11 Reaction can be performed without harnessing electricity!  G of reaction: maximum work over and above volume work (electricity) that can be harnessed from the chemical reaction.

12 Cu wire is dipped into Zn 2+ solution: nothing happens. Cu wire is dipped into Ag + solution: Ag + has higher tendency to be reduced than Cu 2+. Cu 2+ has higher tendency to be reduced than Zn 2+. 2Ag + (aq) + Cu (s) → 2Ag (s) + Cu 2+ (aq)

13 Work harnessed!!

14 Ag + has higher tendency to be reduced than Cu 2+. Cu 2+ has higher tendency to be reduced than Zn 2+. How can we know? Electrode Potential Reflects tendency towards reduction Problem: Only potential difference can be measured between two half-cells.

15 Hydrogen Standard Electrode This electrode used as standard. EMF of all other electrodes measured with reference to this electrode. H 2(g) → 2 H + (aq) +2e -

16 Standard Reduction Potential SHE as anode (Oxidation). The other electrode cathode (Reduction). H 2(g) → 2 H + (aq) +2e - Cu 2+ (aq) + 2e - → Cu (s)

17 Voltage: Potential difference Measured voltage = Potential of reduction electrode - Potential of anode electrode

18 H 2(g) → 2 H + (aq) +2e - Cu 2+ (aq) + 2e - → Cu (s) Cu 2+ (aq) + H 2(g) → Cu (s) + 2H + (aq) Spontaneous at Standard conditions Reduction Potential Cu 2+ (aq) + 2e - → Cu (s) E o red =0.34 V

19 H 2(g) → 2 H + (aq) +2e - Zn 2+ (aq) + 2e - → Zn (s) Zn 2+ (aq) + H 2(g) → Zn (s) + 2H + (aq) Zn (s) → Zn 2+ (aq) +2e - 2 H + (aq) +2e - → H 2(g) Zn (s) + 2H + (aq) → Zn 2+ (aq) + H 2(g)

20 Reduction Potential Zn 2+ (aq) + H 2(g) → Zn (s) + 2H + (aq) nonspontaneous Electricity must be applied to force this process to take place! Zn 2+ (aq) + 2e - → Zn (s) E o red = -0.76 V

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22 Cu 2+ (aq) + 2e - → Cu (s) Zn (s) → Zn 2+ (aq) +2e - Cu 2+ (aq) + Zn (s) → Cu (s) + Zn 2+ (aq)

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24 Electrochemical thermodynamics  G of reaction: maximum work over and above volume work (available work) (electricity) that can be harnessed from the chemical reaction.

25 Electrical heater Heating elements resistive Work done

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35 Concentration Cells Consider the cell presented on the left. The 1/2 cell reactions are the same, it is just the concentrations that differ. Will there be electron flow?

36 Concentration Cells (cont.) AgAg + + e - -E 1/2 Anode: Ag + + e - Ag E 1/2 Cathode: E cell = E° cell - (0.0591/n)log(Q) 0 V E cell = - (0.0591)log(0.1) = 0.0591 V 1

37 Concentration Cells (cont.) Another Example: What is E cell ?

38 Concentration Cells (cont.) E cell = E° cell - (0.0591/n)log(Q) 0 Fe 2+ + 2e - Fe 2 e - transferred…n = 2 2 E cell = -(0.0296)log(.1) = 0.0296 V anodecathode e-e-


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