Electrochemistry Part Four

CHEMICAL CHANGE  ELECTRIC CURRENT To obtain a useful current, we separate the oxidizing and reducing agents so that electron transfer occurs thru an external wire.To obtain a useful current, we separate the oxidizing and reducing agents so that electron transfer occurs thru an external wire. This is accomplished in a GALVANIC or VOLTAIC cell. A group of such cells is called a battery.

Galvanic Cells 19.2 spontaneous redox reaction anode oxidation cathode reduction - +

Galvanic Cells 19.2 The difference in electrical potential between the anode and cathode is called: cell voltage electromotive force (emf) cell potential Cell Diagram Zn (s) + Cu 2+ (aq) Cu (s) + Zn 2+ (aq) [Cu 2+ ] = 1 M & [Zn 2+ ] = 1 M Zn (s) | Zn 2+ (1 M) || Cu 2+ (1 M) | Cu (s) anodecathode

Standard Electrode Potentials 19.3 Zn (s) | Zn 2+ (1 M) || H + (1 M) | H 2 (1 atm) | Pt (s) 2e - + 2H + (1 M) H 2 (1 atm) Zn (s) Zn 2+ (1 M) + 2e - Anode (oxidation): Cathode (reduction): Zn (s) + 2H + (1 M) Zn 2+ + H 2 (1 atm)

Standard Electrode Potentials 19.3 Standard reduction potential (E 0 ) is the voltage associated with a reduction reaction at an electrode when all solutes are 1 M and all gases are at 1 atm. E 0 = 0 V Standard hydrogen electrode (SHE) 2e - + 2H + (1 M) H 2 (1 atm) Reduction Reaction

19.3 E 0 is for the reaction as written The more positive E 0 the greater the tendency for the substance to be reduced The half-cell reactions are reversible The sign of E 0 changes when the reaction is reversed Changing the stoichiometric coefficients of a half-cell reaction does not change the value of E 0

19.3 E 0 = V = 0.76 V cell Standard emf (E 0 ) cell Zn 2+ (1 M) + 2e - Zn E 0 = V E 0 = E H /H + E Zn /Zn cell Standard Electrode Potentials E 0 = E cathode + E anode cell 00 Zn (s) | Zn 2+ (1 M) || H + (1 M) | H 2 (1 atm) | Pt (s) If the reaction is backwards, be sure to flip the sign! +2 So E o Zn/Zn = V +2

Standard Electrode Potentials 19.3 Pt (s) | H 2 (1 atm) | H + (1 M) || Cu 2+ (1 M) | Cu (s) 2e - + Cu 2+ (1 M) Cu (s) H 2 (1 atm) 2H + (1 M) + 2e - Anode (oxidation): Cathode (reduction): H 2 (1 atm) + Cu 2+ (1 M) Cu (s) + 2H + (1 M) E 0 = E cathode + E anode cell 00 E 0 = 0.34 V cell E cell = E Cu /Cu + E H /H = E Cu /Cu E Cu /Cu = 0.34 V 2+ 0

What is the standard emf of an electrochemical cell made of a Cd electrode in a 1.0 M Cd(NO 3 ) 2 solution and a Cr electrode in a 1.0 M Cr(NO 3 ) 3 solution? Cd 2+ (aq) + 2e - Cd (s) E 0 = V Cr 3+ (aq) + 3e - Cr (s) E 0 = V Cd is the stronger oxidizer Cd will oxidize Cr 2e - + Cd 2+ (1 M) Cd (s) Cr (s) Cr 3+ (1 M) + 3e - Anode (oxidation): Cathode (reduction): 2Cr (s) + 3Cd 2+ (1 M) 3Cd (s) + 2Cr 3+ (1 M) x 2 x 3 E 0 = E cathode + E anode cell 00 E 0 = (+0.74) cell E 0 = 0.34 V cell 19.3

19.4 Spontaneity of Redox Reactions  G = -nFE cell  G 0 = -nFE cell 0 n = number of moles of electrons in reaction F = 96,500 J V mol = 96,500 C/mol  G 0 = -RT ln K = -nFE cell 0 E cell 0 = RT nF ln K (8.314 J/K mol)(298 K) n (96,500 J/V mol) ln K = = V n ln K E cell 0 = V n log K E cell 0

Spontaneity of Redox Reactions 19.4

2e - + Fe 2+ Fe 2Ag 2Ag + + 2e - Oxidation: Reduction: What is the equilibrium constant for the following reaction at 25 0 C? Fe 2+ (aq) + 2Ag (s) Fe (s) + 2Ag + (aq) = V n ln K E cell E 0 = E 0 = V V x nE0E0 cell exp K = n = V x 2x V = exp K = 1.23 x E 0 = E Fe /Fe + E Ag /Ag

The Effect of Concentration on Cell Emf  G =  G 0 + RT ln Q  G = -nFE  G 0 = -nFE 0 -nFE = -nFE 0 + RT ln Q E = E 0 - ln Q RT nF Nernst equation At V n ln Q E 0 E = V n log Q E 0 E =

Will the following reaction occur spontaneously at 25 0 C if [Fe 2+ ] = 0.60 M and [Cd 2+ ] = M? Fe 2+ (aq) + Cd (s) Fe (s) + Cd 2+ (aq) 2e - + Fe 2+ 2Fe Cd Cd e - Oxidation: Reduction: n = 2 E 0 = (-0.40) E 0 = V E 0 = E Fe /Fe + E Cd /Cd V n ln Q E 0 E = V 2 ln VE = E = E > 0Spontaneous 19.5

Charging a Battery When you charge a battery, you are forcing the electrons backwards (from the + to the -). To do this, you will need a higher voltage backwards than forwards. This is why the ammeter in your car often goes slightly higher while your battery is charging, and then returns to normal. In your car, the battery charger is called an alternator. If you have a dead battery, it could be the battery needs to be replaced OR the alternator is not charging the battery properly.

Batteries 19.6 Leclanché cell Dry cell Zn (s) Zn 2+ (aq) + 2e - Anode: Cathode: 2NH 4 (aq) + 2MnO 2 (s) + 2e - Mn 2 O 3 (s) + 2NH 3 (aq) + H 2 O (l) + Zn (s) + 2NH 4 (aq) + 2MnO 2 (s) Zn 2+ (aq) + 2NH 3 (aq) + H 2 O (l) + Mn 2 O 3 (s)

Batteries Zn(Hg) + 2OH - (aq) ZnO (s) + H 2 O (l) + 2e - Anode: Cathode: HgO (s) + H 2 O (l) + 2e - Hg (l) + 2OH - (aq) Zn(Hg) + HgO (s) ZnO (s) + Hg (l) Mercury Battery 19.6

Batteries 19.6 Anode: Cathode: Lead storage battery PbO 2 (s) + 4H + (aq) + SO 2- (aq) + 2e - PbSO 4 (s) + 2H 2 O (l) 4 Pb (s) + SO 2- (aq) PbSO 4 (s) + 2e - 4 Pb (s) + PbO 2 (s) + 4H + (aq) + 2SO 2- (aq) 2PbSO 4 (s) + 2H 2 O (l) 4

Batteries 19.6 Solid State Lithium Battery

Batteries 19.6 A fuel cell is an electrochemical cell that requires a continuous supply of reactants to keep functioning Anode: Cathode: O 2 (g) + 2H 2 O (l) + 4e - 4OH - (aq) 2H 2 (g) + 4OH - (aq) 4H 2 O (l) + 4e - 2H 2 (g) + O 2 (g) 2H 2 O (l)

Corrosion 19.7

Cathodic Protection of an Iron Storage Tank 19.7

19.8 Electrolysis is the process in which electrical energy is used to cause a nonspontaneous chemical reaction to occur.

Electrolysis of Water 19.8

Chemistry In Action: Dental Filling Discomfort Hg 2 /Ag 2 Hg V 2+ Sn /Ag 3 Sn V 2+ Sn /Ag 3 Sn V 2+

Electrolysis and Mass Changes charge (Coulombs) = current (Amperes) x time (sec) 1 mole e - = 96,500 C = 1 Faraday 19.8

How much Ca will be produced in an electrolytic cell of molten CaCl 2 if a current of A is passed through the cell for 1.5 hours? Anode: Cathode: Ca 2+ (l) + 2e - Ca (s) 2Cl - (l) Cl 2 (g) + 2e - Ca 2+ (l) + 2Cl - (l) Ca (s) + Cl 2 (g) 2 mole e - = 1 mole Ca mol Ca = C s x 1.5 hr x 3600 s hr96,500 C 1 mol e - x 2 mol e - 1 mol Ca x = mol Ca = 0.50 g Ca 19.8