Example 18-1 The following reactions are spontaneous and thus proceed to the right, as written What can we deduce regarding the strengths of H +, Ag +, Cd 2+, Zn 2+ as electron acceptors? (or oxidizing agents) 493
Chapter18 p 493 Figure 18-1 Photograph of a “ silver tree.” 銅片浸入硝酸銀水溶液中
Chapter18 p 495 Figure 18-2 (a)A galvanic cell at open circuit;
Chapter18 p 495 (b) a galvanic cell doing work;
Chapter18 p 495 (c) an electronlytic cell. 電解電池
Chapter18 p 電池表示方法 18B-3 Representing Cells Schematically Chemists frequently use a shorthand notation to describe electrochemical cells. The cell in Figure 18-2a, for example, is described by single vertical line indicates a phase boundary, or interface, at which a potential develops. The double vertical line represents two phase boundaries, one at each end of the salt bridge. A liquid- junction potential develops at each of these interfaces. 498
Chapter18 p 陽極 (anode) 陰極 (cathode)
Chapter18 p 500 Figure 18-3 Movement of charge in a galvanic cell.
Chapter18 p 18C Electrode Potentials 電極 電位 The cell potential E cell is related to the free energy of the reaction ΔG by 499
Chapter18 p If the reactants and products are in their standard states, the resulting cell potential is called the standard cell potential. where R is the gas constant and T is the absolute temperature. 500
Chapter18 p 501 (a)
Chapter18 p 501 (b)
Chapter18 p 501 (c)
Chapter18 p 503 Figure 18-5 Cell potential in the galvanic cell of Figure 18-4b as a function of time. The cell current, which is directly related to the cell potential, also decreases with the same time behavior.
Chapter18 p If we always follow this convention, the value of E cell is a measure of the tendency of the cell reaction to occur spontaneously in the direction written from left to right. the spontaneous cell reaction will occur. we may write the cell potential E cell as
Chapter18 p 18C-2 The Standard Hydrogen Reference Electrode an electrode must be easy to construct, reversible, and highly reproducible in its behavior. The standard hydrogen electrode (SHE) meets these specifications and has been used throughout the world for many years as a universal reference electrode. It is a typical gas electrode. The half-reaction responsible for the potential that develops at this electrode is 504
Chapter18 p Figure 18-6 The hydrogen gas electrode. 505 By convention, the potential of the standard hydrogen electrode is assigned a value of 0.000 V at all temperatures.
Chapter18 p Standard Electrode Potentials 標準電極電位 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)
Chapter18 p 18C-3 Electrode Potential and Standard Electrode Potential An electrode potential is defined as the potential of a cell in which the electrode in question is the right-hand electrode and the standard hydrogen electrode is the left-hand electrode. The cell potential is E Ag is the potential of the silver electrode. p.505
Chapter18 p The standard electrode potential, E 0, of a half- reaction is defined as its electrode potential when the activities of the reactants and products are all unity. the E 0 value for the half-reaction the cell shown in Figure 18-7 can be represented schematically as 506
Chapter18 p 506 Figure 18-7 Measurement of the electrode potential for an Ag electrode. If the silver ion activity in the right- hand compartment is 1.00, the cell potential is the standard electrode potential of the Ag + /Ag half- reaction.
Chapter18 p This galvanic cell develops a potential of 0.799 V with the silver electrode the standard electrode potential is given a positive sign, and we write 506
Chapter18 p 18C-5 Effect of Concentration on Electrode Potentials: The Nernst Equation Consider the reversible half-reaction 508
Chapter18 p E 0 = the standard electrode potential, which is characteristic for each half-reaction R = the ideal gas constant, 8.314 J K － 1 mol － 1 T = temperature, K n = number of moles of electrons that appears in the half-reaction for the electrode process as written F = the faraday 96,485 C (coulombs) per mole of electrons If we substitute numerical values for the constants, convert to base 10 logarithms, and specify 25°C for the temperature, we get 509
Chapter18 p Nernst equation p.509 If we substitute numerical values for the constants, convert to base 10 logarithms, and specify 25°C for the temperature, we get
Chapter18 p 1.The standard electrode potential is a relative quantity in the sense that it is the potential of an electrochemical cell in which the reference electrode is the standard hydrogen electrode, whose potential has been assigned a value of 0.000 V. 2.The standard electrode potential for a half-reaction refers exclusively to a reduction reaction; 3.The standard electrode potential measures the relative force tending to drive the half-reaction from the reactants and products are at their equilibrium activities p.511 18C-6 The Standard Electrode Potential, E 0 511 4.The standard electrode potential is independent of the number of moles of reactant and product shown in the balanced half- reaction.
Chapter18 p 5.A positive electrode potential indicates that the half- reaction in question is spontaneous with respect to the standard hydrogen electrode half-reaction. 6.The standard electrode potential for a half-reaction is temperature dependent.
Chapter18 p 512
Chapter18 p System involving precipitates or complex ions
Chapter18 p Ch 19 Applications of Standard Electrode Potentials
EXAMPLE 19-1 Calculate the thermodynamic potential of the following cell and the free energy change associated with the cell reaction. 395 計算下列電池的電位與自由能變化量
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) = 0.0257 V n ln K E cell 0 19.4 n = 2
EXAMPLE 19-2 Calculate the potential of the cell
EXAMPLE 19-3 Calculate the potential of the following cell and indicate the reaction that would occur spontaneously if the cell were short circuited (Figure 19-1). p 525
EXAMPLE 19-4 Calculate the cell potential for Note that this cell does not require two compartments (nor a salt bridge) because molecular H 2 has little tendency to react directly with the low concentration of Ag ＋ in the electrolyte solution. This is an example of a cell without liquid junction (Figure 19-2). p.526 計算下列電池的電位
EXAMPLE 19-5 Calculate the potential for the following cell using (a) concentration (b) activity where x = 5.00x10 -4, 2.00x10 -3, 1.00x10 -2, and 5.00x10 -2 計算下列電池的電位 (a) concentration
EXAMPLE 19-5 Calculate the potential for the following cell using (a) concentration (b) activity where x = 5.00x10 -4, 2.00x10 -3, 1.00x10 -2, and 5.00x10 -2 計算下列電池的電位 (b) activity 活性
EXAMPLE 19-6 Calculate the potential required to initiate deposition of copper from a solution that is 0.010 M in CuSO 4 and contains sufficient H 2 SO 4 to give a pH of 4.00. The deposition of copper necessarily occurs at the cathode. Since there is no more easily oxidizable species than water in the system, O 2 will evolve at the anode.
EXAMPLE 19-7 D. A. MacInnes found that a cell similar to that shown in Figure 19-2 had a potential of 0.52053 V. The cell is described by the following notation. Calculate the standard electrode potential for the half-reaction (by activities)
19C CALCULATING REDOX EQUILIBRIUM CONSTANTS （氧化還原反應的平衡常數） Thus, at chemical equilibrium, we may write or We can generalize Equation 19-6 by stating that at equilibrium, the electrode potentials for all half- reactions in an oxidation/reduction system are equal. p.534
EXAMPLE 19-8 Calculate the equilibrium constant for the reaction shown in Equation 19-4 at 25°C. p.535
EXAMPLE 19-9 Calculate the equilibrium constant for the reaction
EXAMPLE 19-10 Calculate the equilibrium constant for the reaction Again we have multiplied both equations by integers so that the numbers of electrons are equal. When this system is at equilibrium. p.538