Ebook Electrochemical methods Fundamentals and applications (2nd edition) Part 2

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Ebook Electrochemical methods  Fundamentals and applications (2nd edition) Part 2

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(BQ) Part 2 book Electrochemical methods Fundamentals and applications has contents: Electrode reactions with coupled homogeneous chemical reactions, electrode reactions with coupled homogeneous chemical reactions, electrode reactions with coupled homogeneous chemical reactions, photoelectrochemistry and electrogenerated chemiluminescene, electrochemical instrumentation,...and other contents.

CHAPTER 12 ELECTRODE REACTIONS WITH COUPLED HOMOGENEOUS CHEMICAL REACTIONS 12.1 CLASSIFICATION OF REACTIONS The previous chapters dealt with a number of electrochemical techniques and the responses obtained when the electroactive species (O) is converted in a heterogeneous electron-transfer reaction to the product (R) This reaction is often a simple one-electron transfer, such as an outer-sphere reaction where no chemical bonds in species О are broken and no new bonds are formed Typical reactions of this type are Fe(CN)^" + e [Cp*Re(CO)2(p-N2C6H4OMe)] -^ Cp*Re(CO) N + C H OMe in n Co Br en + 6H O + e -> Co (H O) + 2Br~ + 2en (12.1.11a) (12.1.11b) (where Cp* = 77 -СзМе5 and en = ethylenediamine) In many cases, the product formed in the following reaction can undergo an additional electron-transfer reaction, leading to an ECE sequence, discussed in Section 12.1.2(b) (c) Catalytic (EC) Reaction O + ne ±± R t (12.1.12) , I R + Z -> O + Y (12.1.13) A special type of EC process involves reaction of R with a nonelectroactive species, Z, in solution to regenerate О (Figure 12.1.1, path 8) If species Z is present in large excess compared to O, then (12.1.13) is a pseudo-first-order reaction An example of this 12.1 Classification of Reactions 475 scheme is the reduction of Ti(IV) in the presence of a substance that can oxidize Ti(III), suchasNH OHorClO^: Ti(IV) + e > Ti(III) t I СЮ3-, NH OH (12.1.14) Since hydroxylamine and chlorate ion can be reduced by Ti(III), they should be reducible directly at the mercury electrode at the potentials needed to generate Ti(III); however, the direct reductions not occur because the rates at the electrode are very small Other examples of E C reactions are the reduction of Fe(III) in the presence of H O and the oxidation of I~ in the presence of oxalate An important E C reaction involves reductions at mercury where the product can reduce protons or solvent (a so-called "catalytic" hydrogen reaction) 12.1.2 Reactions with Two or More E Steps (а) ЕЕ Reaction A + £?*=> В В +

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  • PREFACE

  • CONTENTS

  • MAJOR SYMBOLS

  • Chapter 1 Introduction and overview of electrode processes

    • 1.1 Introduction

    • 1.2 Nonfaradaic Processes And The Nature Of The Electrode-Solution Interface

    • 1.5 Semiempirical Treatment Of Nernstian Reactions With Coupled Chemical Reactions

    • 1.6 The Literature Of Electrochemistry

    • 1.7 References

    • 1.8 Problems

    • Chapter 2 Potentials And Thermodynamics Of Cells

      • 2.1 Basic Electrochemical Thermodynamics

      • 2.2 A More Detailed View Of Interfacial Potential Differences

      • 2.3 Liquid Junction Potentials

      • 2.4 Selective Electrodes

      • 2.5 References

      • 2.6 Problems

      • Chapter 3 Kinetics Of Electrode Reactions

        • 3.1 Review Of Homogeneous Kinetics

        • 3.2 Essentials Of Electrode Reactions

        • 3.3 Butler-Volmer Model Of Electrode Kinetics

        • 3.4 Implications Of The Butler-Volmer Model For The One-Step, One-Electron Process

        • 3.5 Multistep Mechanisms

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