Nernst equation E = Eө - lnQ Eө = -

Slides:



Advertisements
Similar presentations
ΔG of an Electrochemical Cell The change in Gibbs Energy ΔG is the maximum non-PV work* that can be obtained from a chemical reaction at constant T and.
Advertisements

Chemistry 232 Electrochemistry. A Schematic Galvanic Cell Galvanic cells – an electrochemical cell that drives electrons through an external circuit spontaneous.
SOLUTIONS TO EXAMPLES.
Author: J R Reid Electrochemical Cells – Voltage (Electric potential) The half cells Standard electrode potentials Calculating voltages Examples.
Chapter 20 Electrochemistry.
Oxidation-Reduction (Redox) Reactions
Lecture 263/30/07. E° F 2 (g) + 2e - ↔ 2F Ag + + e - ↔ Ag (s)+0.80 Cu e - ↔ Cu (s)+0.34 Zn e - ↔ Zn (s)-0.76 Quiz 1. Consider these.
Copyright©2000 by Houghton Mifflin Company. All rights reserved. 1 Electrochemistry The study of the interchange of chemical and electrical energy.
University of Kentucky
Midterm Exam 1: Feb. 2, 1:00- 2:10 PM at Toldo building, Room 100.
Chapter 18 Electrochemistry
Predicting Spontaneous Reactions
The End is in Site! Nernst and Electrolysis. Electrochemistry.
TO CATCH LOTS OF FISH, YOU MUST FIRST GO TO THE WATER. -ANON-
Electrochemistry Chapter 19.
Redox Reactions and Electrochemistry
Redox Reactions and Electrochemistry
Concentration Cells M | M + (aq, L) || M + (aq, R) | M Cell reaction: M + (aq, R) → M + (aq, L) since Δ r G θ = 0 (why?)
The determination of equilibrium constants Self-test 7.11 Calculate the solubility constant (the equilibrium constant for reaction Hg 2 Cl 2 (s) ↔ Hg 2.
8–1 Ibrahim BarryChapter 20-1 Chapter 20 Electrochemistry.
Chapter 20 Electrochemistry and Oxidation-Reduction.
Electrochemistry: Oxidation-Reduction Reactions Zn(s) + Cu +2 (aq)  Zn 2+ (aq) + Cu(s) loss of 2e - gaining to 2e - Zinc is oxidized - it goes up in.
Oxidation-Reduction Reactions Chapter 4 and 18. 2Mg (s) + O 2 (g) 2MgO (s) 2Mg 2Mg e - O 2 + 4e - 2O 2- _______ half-reaction (____ e - ) ______________________.
Redox Reactions & Electrochemistry Chapter 19 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Tutorial schedule (3:30 – 4:50 PM) No. 1 (Chapter 7: Chemical Equilibrium) January 31 at Biology building, room 113 February 1 at Dillion Hall, room 254.
Nernst Equation Walther Nernst
Unit 16 Electrochemistry Oxidation & Reduction. Oxidation verses Reduction Gain oxygen atoms 2 Mg + O 2  2 MgO Lose electrons (e - ) Mg (s)  Mg + 2.
Electrochemistry Part Four. CHEMICAL CHANGE  ELECTRIC CURRENT To obtain a useful current, we separate the oxidizing and reducing agents so that electron.
Free Energy ∆G & Nernst Equation [ ]. Cell Potentials (emf) Zn  Zn e volts Cu e-  Cu volts Cu +2 + Zn  Cu + Zn +2.
Chemsheets AS006 (Electron arrangement)
Electrochemistry is the branch of chemistry that deals with the use of chemical reaction to generate a potential or voltage.
Standard Reduction Potentials Its all about ~~ SHE!
Nerst equation E = Eө - lnQ Eө = -
ELECTROCHEMICAL CELLS Chapter 20 : D8 C20
CHAPTER 18 Electrochemistry.
Oxidation-Reduction Chemistry
17.1 Galvanic Cells (Batteries)
ELECTROCHEMISTRY.
Electrochemistry Chapter 19
Electrochemistry.
Principles & Modern Applications
Electrochemistry Chapter 20.
Zn(s) + CuSO4(aq)→ ZnSO4 (aq) + Cu(s)
The Study of the Interchange of Chemical and Electrical Energy
Lab 9: Electrochemistry
Chapter 20 - Electrochemistry
Dr. Aisha Moubaraki CHEM 202
Electrochemistry Applications of Redox.
Redox Reactions and Electrochemistry
Chapter 20 Electrochemistry
Electrochemical cells
Cell Potential and the Nernst Equation
CHAPTER 15 Electro-chemistry 15.4 Electrochemical Cells.
Chapter 17: Electrochemistry
Chapter 15 Oxidation and Reduction
Electrochemistry.
Chapter 17 Electrochemistry
Standard Reduction (Half-Cell) Potentials
Electrochemistry Applications of Redox.
Recall the definition of standard cell potential understand the need for a reference electrode Calculate the standard cell potential.
Applications of standard potentials
Electrochemistry Lesson 7 The Standard Hydrogen Cell.
Electrochemistry Chapter 18.

Chapter 20: Electrochemistry
Applications of standard potentials
EQUILIBRIUM AND SPONTANEITY
Presentation transcript:

Nernst equation E = Eө - lnQ Eө = - At 25 oC, the Nernst equation can be simplified further: E = Eө - lnQ Under equilibrium condition: Q = K, and E = 0 so lnK = Eө*v/25.7mV

Concentration Cells Cell reaction: M+(aq, R) → M+(aq, L) E = M | M+(aq, L) || M+(aq, R) | M Cell reaction: M+(aq, R) → M+(aq, L) E = since ΔrGθ = 0 (why?)

The cell emf The standard emf of a cell can be calculated by the difference of the standard potentials of the two electrodes. Consider: Ag(s)|Ag+(aq) || Cl-(aq) |AgCl(s)| Ag(s) The overall potential of the cell is: Eθ = Eθ(AgCl/Ag, Cl-) – Eθ(Ag+/Ag) In a general form: Eθ = Eθ(right) – Eθ(left) Example: Calculate the standard voltage for the cell: Mn+2|Mn+3||Fe+3|Fe+2 Solution: First, separate the cell into two half reactions Reduction: Fe+3(aq) + e- → Fe+2(aq) Reduction: Mn+3(aq) + e- → Mn+2(s) To compute the cell voltage, simply use the right-hand electrode subtract the left-hand electrode. E θ = E θ right - E θleft = 0.769 - (1.51) = - 0.741 V (???)

Calculating equilibrium constant from the standard emf Example: Evaluate the solubility constant of silver chloride, AgCl, from cell potential data at 298.15K. Solution: AgCl(s) → Ag+(aq) + Cl-(aq) Establish the electrode combination: Right: AgCl + e- → Ag(s) + Cl-(aq) Eθ = 0.22V Left: Ag+(aq) + e- → Ag(s) Eθ = 0.80V The standard emf is : Eθ (right) – Eθ(Left) = - 0.58V lnK = = 0.58/0.025693 K = 1.6x10-10

The measurement of standard potentials The potential of standard hydrogen electrode: Pt(s)|H2(g)|H+(aq) is defined as 0 at all temperatures. The standard potential of other electrodes can be obtained by constructing an electrochemical cell, in which hydrogen electrode is employed as the left-hand electrode (i.e. anode) Example: the standard potential of the AgCl/Ag couple is the standard emf of the following cell: Pt(s)|H2(g)|H+(aq), Cl-(aq)|AgCl(s)|Ag(s) or Pt(s)|H2(g)|H+(aq) || Cl-(aq)|AgCl(s)|Ag(s) with the cell reaction is: ½ H2(g) + AgCl(s) → H+(aq) + Cl-(aq) + Ag(s)

ΔrG = ΔrGθ + RTln According to Nernst equation: –vFE = -vFE θ + RTln Using the molality and the activity coefficient to represent the activity: E = E θ – (RT/vF)ln(b2) - (RT/vF)ln(γ±2) Reorganized the above equation: E + (2RT/vF)ln(b) = E θ - (2RT/vF)ln(γ±) Since ln(γ±) is proportional to b1/2, one gets E + (2RT/vF)ln(b) = E θ - C* b1/2, C is a constant Therefore the plot of E + (2RT/vF)ln(b) against b1/2 will yield a straight line with the interception corresponds to E θ

Example plot from the text book

Example: Devise a cell in which the cell reaction is Mg(s) + Cl2(g) → MgCl2(aq) Give the half-reactions for the electrodes and from the standard cell emf of 3.00V deduce the standard potential of the Mg2+/Mg couple. Solution: the above reaction indicates that Cl2 gas is reduced and Mg is oxidized. Therefore, R: Cl2(g) + 2e- → 2Cl-(aq) (Eө = + 1.36 from Table 10.7) L: Mg2+(aq) + 2e- → Mg(s) The cell which corresponds to the above two half-reaction is : Mg(s)|MgCl2(aq)|Cl2(g)|Pt Eөcell = Eө(R) - Eө(L) = 1.36 – Eө(Mg2+, Mg) Eө(Mg2+, Mg) = 1.36V – 3.00V = - 1.64V

Example: What is the standard voltage for the cell Example: What is the standard voltage for the cell Mn|Mn+2||Fe+3|Fe+2|Pt Solution: First, separate the cell into two reduction half reactions Right: Fe+3(aq) + e- → Fe+2(aq) Left: Mn+2(aq) + 2e- → Mn(s) Note that the above two half reactions have different number of electrons being transferred! To calculate the cell emf, write done the cell reaction and go through the standard reaction Gibbs energy. The following cell reaction is obtained via 2*R – L, 2Fe+3(aq) + Mn(s) → 2Fe+2(aq) + Mn+2(aq) should the standard cell potential be calculated as 2*Eө(R) - Eө(L) ? Consider: ΔrGθ = 2ΔrGθ (R) - ΔrGθ(L) 2FE θ = 2(1*F* E θ (R) – 2*F* E θ (L) it leads to Eөcell = Eө(R) - Eө(L) = 0.769 - (- 1.182) = 1.951 V

Example: Consider a hydrogen electrode in aqueous HCl solution at 25oC operating at 105kPa. Calculate the change in the electrode potential when the molality of the acid is changed from 5.0 mmol kg-1 to 50 mmol kg-1. Activity coefficient can be found from Atkin’s textbook (Table 10.5 ). Solution: first write down the half reaction equation: H+(aq) + e- → ½ H2(g) Based on Nernst equation E = Eө - ln(Q) Q = So E = - ln( ) E2 – E1 = - ln( ) = - 25.7(mV)x ln( ) = 56.3 mV

In the lead storage battery, Pb | PbSO4 | H2SO4 | PbSO4, PbO2 | Pb would the voltage change if you changed the concentration of H2SO4? (yes/no) Answer ... Hint... The net cell reaction is Pb + PbO2 + 2HSO4- + 2H+ → 2 PbSO4 + 2 H2O The Nernst equation ΔE = Δ E° - (0.0592/2)log{1/{[HSO4-]2[H+]2}}.

Choose the correct Nernst equation for the cell Zn(s) | Zn2+ || Cu2+ | Cu(s). A: Δ E = Δ E° - 0.0296 log([Zn2+ ]/[Cu2+]) B: Δ E = Δ E° - 0.0296 log([Cu2+] / [Zn2+]) C: Δ E = Δ E° - 0.0296 log(Zn / Cu) D: Δ E = Δ E° - 0.0296 log(Cu / Zn) Answer ... Hint... The cell as written has Reduction on the Right: Cu2+ + 2e = Cu oxidation on the left: Zn = Zn2+ + 2e Net reaction of cell is Zn(s) + Cu2+ = Cu(s) + Zn2+