Electrochemistry_basics.pdf

Electrochemistry Basics Table of Contents 1. Introduction 2. Voltaic Cells-Galvanic Cells 3. Cell Potential 4. Balancing Redox Reactions 5. Rules for Assigning Oxidation states 6. Additional Materials 6.1. I. Conversion 6.2. II. Free Energy & Cell Potential 6.3. III. Nernst equation 6.4. At Equilibr...

Electrochemistry Basics Table of Contents 1. Introduction 2. Voltaic Cells-Galvanic Cells 3. Cell Potential 4. Balancing Redox Reactions 5. Rules for Assigning Oxidation states 6. Additional Materials 6.1. I. Conversion 6.2. II. Free Energy & Cell Potential 6.3. III. Nernst equation 6.4. At Equilibrium 7. Terminology 8. Reference 9. Outside Links 10. Contributors As the name suggests, electrochemistry is the study of changes that cause electrons to move. This movement of electrons is called electricity. In electrochemistry, electricity can be generated by movements of electrons from one element to another in a reaction known as a redox reaction or oxidation-reduction reaction. Introduction A redox reaction is a reaction which involves a change in oxidation state of one or more elements. When a substance loses its electron, its oxidation state increases, thus it is oxidized. When a substance gains an electron, its oxidation state decreases thus being reduced. For example, for the redox reaction: H2+F2→2HF Rewrite it as Oxidation: H2→2H++2e− Reduction: F2+2e−→2F− Overall Reaction : H2+F2→2H++2F− Oxidation reaction lose electrons thus they are being oxidized, while Reduction is gaining electrons thus they are being reduced. In this case, H2 is being oxidized, while F2 is being reduced. OIL RIG Oxidation Is Losing electrons Reduction Is Gaining electrons E Fe-V Couple Voltaic Cells-Galvanic Cells In 1793, Alessandro Volta discovered that electricity could be produced by placing different metals on the opposite sides of a wet paper or cloth. He made his first battery by placing Ag and Zn on the opposite sides of a moistened cloth with salt or weak acid solution. Therefore, these batteries got the name Voltaic Cells. Voltaic (Galvanic) Cells are electrochemical cells which contain a spontaneous reaction, and always have a positive voltage. The electrical energy released during the reaction can be used to do work. A voltaic cell consists of two compartments called half-cells. The half-cell where oxidation occurs is called anode. The other half-cell where reduction occurs is called cathode. The Electrons in voltaic cells flow from the negative electrode to the positive electrode, which flows from anode to cathode.(See, figure below) (Note: electrodes=where the oxidation/reduction reactions occur). Red Cat and An Ox Reduction Cathode and Anode Oxidation is a helful way to remember which reaction occurs on which half cell. In order for oxidation-reduction reaction to occur, the two substances in each respective half-cell are connected by closed circuit so that electrons can flow from the reducing agent to the oxidizing agent. It also needs a salt bridge so that reaction can keep proceeding. Galvanic Cell Needs electrical current from outside for it to work: xample 1: Notice how there is a voltmeter. Galvanic cell take energy sources from outside to make itself work. The figure above shows that Zn(s) is continuously oxidized, producing Zn 2+ into the solution. Zn(s)--> Zn2+(aq)+2e-. Conversely, in the cathode, Cu2+ is reduced and continuously deposits on to the Cu(s) metal bar Cu 2+(aq)+2e--->Cu(s). As a result, the solution containing Zn(s) becomes more positively charged while the solution containing Cu(s) becomes more negatively charged. In order for the voltaic cell to work, the solutions in the two half-cells must remain electrically neutral. Therefore, a salt bridge containing KNO3 is added to keep the solutions neutral by adding NO3-, an anion into the anode solution and K+, a cation into the cathode solution. As oxidation and reduction proceed, ions from the salt bridge migrate to neutralize charge in the cell compartments. The diagram of this electrical cell : Zn(s) │Zn2+(aq) ║ Cu2+(aq) │ Cu(s) -use ║ to separate anode(-) and cathode(+) and so represents the salt bridge in between. -use │to separate different states of matter on the same side -use , to separate same states of matter on the same side. Example: │Fe2+(aq),Fe3+(aq)║Ag+(aq) │ Ag(s)  The anode (where the oxidation occurs) is placed on the left side of the ║  The cathode (where reduction occurs) is placed on the right side of the ║ Practice problem: Write out the Electrical cell diagram for this reaction: Cu(s) + 2Ag+(aq) →Cu2+ + 2Ag(s) (aq) Answer key: Cu(s) │Cu2+(aq) ║ Ag+(aq) │ Ag(s) Cell Potential The oxidation of Zn(s) into Zn2+ and the reduction of Cu2+ to Cu(s) occur spontaneously. In other words, the redox reaction between Zn and Cu2+ is spontaneous. This is caused by the difference in potential energy between the two substances. The difference in potential energy between the anode and cathode dictates the direction of electrons movement. Electrons move from area of higher potential energy to area of lower potential energy. In this case, the anode has a higher potential energy so electrons move from anode to cathode. The potential difference between the two electrodes is measured in units of volts. One volt (V) is the potential difference necessary to generate a charge of 1 coulomb (C) from 1 Joule (J) of energy. For a voltaic cell, this potential difference is called the cell potential, and is denoted Ecell. For a spontaneous reaction, Ecell is positive and ΔG (Gibbs free energy that can be used to determine if a reaction occurs spontaneously) is negative. Thus, when ΔG is negative the reaction is spontaneous. By merging electrochemistry with thermodynamics we get this formula: ΔG= −n× F × Ecell(or EMF). EMF= Electromotive Force. Cell potential is different for each voltaic cell, its value depends upon the concentrations of specific reactants and products as well as temperature of the reaction. For standard cell potential, temperature of the reaction is assumed to be at 25o Celsius, the concentration of the reactants and products is 1M and reaction occurs at 1 atm pressure. The standard cell potential is denotedEocell. The can be written = oxidation potential + reduction potential. For Voltaic cells it will be Eocell=Eo(cathode)-Eo(Anode) Since the values of the standard potential are given in the form of standard reduction potential for each half-reaction, in order to calculate the standard cell potential Eocell, we need to find out which substance is being oxidized, then subtract the standard reduction potential of the oxidation reaction from the standard reduction potential of the reducing reaction. For example: Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s) From the equation above, we know that Zn is being oxidized, and Cu is being reduced. For the redox reaction above, the potential for the two half reaction is given in the reduction form: Zn(s) → Zn2+(aq) + eCu2+(aq) + e- → Cu(s) By looking at it's cell potential we can know which one is anode and cathode. Cathode has a more positive potential energy, thus Cu is the cathode Zn is the anode. In order to calculate Eocell, subtract Zn of the oxdized species from the Cu of the reduced species, which is Eo (cathode)-E(Anode) (Note: Keep Cell potential in reduction form) cell = Oxidation: Zn(s) → Zn2+(aq) + eReduction: Cu2+(aq) + e- → Cu(s) - Eo= +0.763V Eo= +0.340V Or, you can rewrite the anode half reaction into it's oxidation form, then add to the reduction half reaction of cathode to find Eocell: Oxidation: Zn2+(aq) + e- → Zn(s) Reduction: Cu2+(aq) + e- → Cu(s) Eo= -0.763V Eo= +0.340V Net: Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s) Eocell = +0.340V + (-0.763V) = -.423V Since standard reduction potential have intensive properties, so changing the stoichiometric coefficient in a half reaction does not affect the value of the standard potential. For example, Oxidation:{Al(s) → Al3+(aq) +3e-} x 2 Reduction:{Sn2+(aq) +2e- → Sn(s)} x 3 is still is still Eo= -1.676 Eo= -0.137 When multiplying the stoichiometric coefficient by 2, the standard potential does not change: Balancing Redox Reactions Method 1: Oxidation Number Method      Step 1: Assign oxidation numbers of each atom. Step 2: Determine the net change in charge to determine the ratio of atoms Step 3: Use the ratio to eliminate the net charge change Step 4: Use the ratio as coefficients for the elements Step 5: Use inspection to finish balancing of the equation Method 2: Half-Reaction Method      Step 1: Determine oxidation numbers for each atom Step 2: Use oxidation numbers to determine what’s oxidized and what’s reduced. Step 3: Write a half-reaction for reduction Step 4: Write a half-reaction for oxidation Step 5: Balance all elements except H and O - if have acid redox reaction: Balance the O using H20, balance the H using protons - if have base redox reaction: Balance O using OH-     Step 6: Sum up the charge in each side Step 7: Balance the charges by adding electrons Step 8: Multiply the half-reactions by factors that cancel out electrons Step 9: Add the two half-reactions back together to eliminate out intermediates Rules for Assigning Oxidation states 1. 2. Free elements have an oxidation state of 0. (e.g., He, N2, O2 has an oxidation state of 0) + The oxidation state of one atom ion must equal to the net charge. ( Ex: F- oxidation state is -1, K oxidation state is +1) 3. The sum of the oxidation state has to equal the total net charge for a compound. (Ex: MnO4 has a net charge of -1, 4. Mn(+7)O4(-8)= -1) The Alkali metals (Group I elements) have an oxidation state of +1. (EX: Li2O, Li= +1) 5. 6. The Alkaline earth metals (Group II elements) always have an oxidation state of +2. (Ex: CaO, Ca=+2) Oxygen has an oxidation state of -2 in a compound 7. 8. Fluorine has an oxidation state of -1 in a compound Hydrogen has an oxidation state of +1 in a compound. 9. Transition metals and other metals may have more than one common ionic charge. ( EX: Chromium common ionic charge are Cr+2 and Cr+3) Practice problem: What is the oxidation state for MgF2 Answer key: MgF2 total charge=0 Total Charge=(+2)+(-1*2)=0 Using rule 4 and 7. Practice problem: What is the oxidation state of H2O Answer key: H2O total charge=0 Total Charge=(+1*2)+(-2)=0 Using rule 6 and 8 Additional Materials I. Conversion 1 amp (A) = 1 Coulomb/sec (C/s) 1 Faraday (F) = 1 mole of e-1 1 Faraday (1 mole of e-1) = 96475 Coulomb (C) II. Free Energy & Cell Potential -flow of electrons that the cell produces can do work -free energy is the E available to do work or maximum work that can be done by system -free energy equation: ΔG= −n× F × EMF ΔG = free energy (usually in J) n = mole of electrons F = 1 Faraday EMF = cell potential. -the negative sign in front of n ensures that the reaction will be spontaneous III. Nernst equation -equation: EMF = EMFo (-RT/nF)ln Q EMF = cell potential at current conditions EMF° = cell potential at standard state (usually at 25 degree Celsius) R = 8.31 J/mole×K T = Kelvin temperature n = mole of electron F = 1 Faraday Q = reaction quotient (Product/Reactant) -relates cell potential and reaction quotient At Equilibrium equation: ln K = (n)(F)(EMFo)/(RT) EMF = 0, Q = K, K = equilibrium constant -cell stops and remains at rest, and will continue to do so until something reactivate it The cell reaction is spontaneous in the forward direction if Ecell>0, ΔG