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Electrochemistry

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Title: Electrochemistry


1
Electrochemistry
  • Electrochemistry is a branch of chemistry that
    deals with electrically related applications of
    redox reactions.
  • Reduction-oxidation reactions involve the
    transfer of electrons.
  • Oxidation means the losing of electrons and
    reduction means the gaining of electrons. The 2
    occur together, they are opposite sides of the
    same coin.
  • For example when zinc is in contact with a
    copper II sulfate solution, the zinc strip loses
    electrons to the copper ions in solution. The
    copper ions accept the electrons and fall out of
    solution. As electrons are transferred between
    zinc atoms and copper ions energy is released as
    heat when the reactions are separated we can
    set them up so that instead of heat energy we can
    get electrical energy.

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Example 1
  • Net ionic equation
  • Zn (s) Cu2 (aq) ? Cu (s) Zn2
    (aq)
  • Oxidation
  • Reduction

4
Voltaic (Galvanic) Cells
  • An electrochemical cell, such as a voltaic cell,
    consists of 2 electrodes. Each electrode is in
    contact with an electrolyte. The 2 electrodes are
    connected by a conducting wire or a circuit. And
    a porous barrier separates the 2 half reactions
    (or half cells).
  • A voltaic cell specifically deals with a
    spontaneous redox reaction as the source of
    energy. It converts chemical energy into
    electrical energy.

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How it works
  • In the wet voltaic cell represented in the
    previous slide an electric current can run
    through an external connecting wire so that the
    electric current moves in closed loop path
    (closed circuit).
  • The electrode where oxidation occurs is called
    the anode.
  • The electrode where reduction occurs is called
    the cathode.
  • The 2 half-reactions occur at the same time but
    in different places at the cell (the porous
    barrier separates them). A salt bridge is
    necessary to keep the half cells electrically
    balanced so that a charge does not build up in
    the cell and stop the electrochemical reaction
    prematurely this salt bridge allows for the
    passage of ions in the cell.

7
  • ANode, OXidation REDuction, CAThode
  • AN OX and a RED CAT

8
Zinc Copper
9
Cell Notation
  • When these cells are represented they are written
    as follows
  • Anode electrode anode solution cathode
    solution cathode electrode
  • Example 2 Write the cell notation for the
    following reaction
  • Zn (s) Cu2 (aq) ? Cu (s) Zn2
    (aq)
  • Zn(s)Zn2 (aq) Cu2 (aq) Cu(s)

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Inactive Electrodes
graphite I-(aq) I2(s) H(aq), MnO4-(aq),
Mn2(aq) graphite
12
Practice Problems
  • Write the half reaction in which I- (aq) changes
    to I2 (s). Identify if this occurs at the anode
    our cathode.
  • Nickel solid is oxidized in to Ni2 ions in a
    voltaic cell while the Cu2 ion are being reduced
    in to copper solid atoms.
  • Write the half reactions
  • Write the net ionic equation
  • Identify the anode and cathode
  • Write the cell notation

13
Cell Voltage
  • The cell voltage from a redox reaction is
    referred to as the standard voltage, Eo (unit
    volts, V).
  • Standard conditions are 1 atm and 1 M solutions
  • Example 3 Zinc metal is placed in hydrochloric
    acid. Zinc is the anode and hydrogen gas forms at
    the cathode. The reaction gives off a standard
    voltage of 0.762 V. Write the net ionic equation
    for this reaction

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Standard Voltage
  • When calculating the standard voltage the
    standard voltage from the reduction and oxidation
    reactions must be considered. So when calculating
    the standard voltage you must use the following
    formula
  • Eo Eored Eoox

17
Standard Potentials
  • The standard half cell (half redox reaction)
    voltages are referred to as standard potentials
    and are used to calculate the standard voltage.
  • Standard Reduction Potentials
  • (one of your equation sheets)
  • This table gives the standard reduction
    potentials, the standard oxidation potentials are
    the same magnitude but the reverse sign.

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When Calculating Cell Voltage
  • When calculating cell voltages there are 2 main
    points to remember
  • 1. the calculation of E , is always a positive
    quantity for a voltaic cell (spontaneous
    reaction).
  • 2. The standard cell voltage is independent of
    how the equation for the cell reaction is
    written. This means you must never multiply the
    voltage by the coefficients used to balance the
    chemical equation.

20
Example
  • Example 4 Use standard reduction potentials to
    calculate the standard voltage for the Zn-H
    cell from example 3.

21
  • The Pain of a Dental Voltaic Cell
  • Have you ever felt a jolt of pain when biting
    down with a filled tooth on a scrap of foil left
    on a piece of food? Heres the reason. The
    aluminum foil acts as an active anode (E of Al
    - 1.66 V), saliva as the electrolyte, and the
    filling (usually a silver/tin/mercury alloy) as
    an inactive cathode. O2 is reduced to water, and
    the short circuit between the foil in contact
    with the filling creates a current that is sensed
    by the nerve of the tooth.

22
Finding Eored or Eoox
  • If the standard voltage and the cell voltage from
    either the reduction or oxidation reaction the
    other maybe found by a simple rearrangement.
  • Example 4 If the standard voltage gathered from
    the standard Zn-Cu2 cell is 1.101 V and the Eoox
    0.762 V, then find the Eored.

23
Reducing Oxidizing Agents
  • If a species undergoes reduction (gains
    electrons) then it is the oxidizing agent. If it
    undergoes oxidation (loses electrons) then it is
    the reducing agent.
  • The stronger the attraction for electrons the
    stronger the oxidizing agent. Or if using the
    standard reduction potentials, the more positive
    the Eored the stronger the oxidizing agent
    (oxidizing strength would be the opposite if
    using the reduction potential table).

24
Cell Voltage Gibbs Free Energy Equilibrium
  • Standard cell voltage and standard free energy
    are related by the following equation
  • Go -nFEo
  • When Go lt 0 and Eo gt 0 the reaction is
    spontaneous.
  • Standard cell voltage and equilibrium are related
    by the following equation
  • Eo RTlnK
  • nF
  • or at standard conditions (25o C)
  • Eo 0.0257 V lnK
  • n
  • When K gt 1 the reaction is spontaneous

25
Effect of Concentration
  • Voltage will increase for a reaction if the
    concentration of the reactants is increased or
    that of the products is decreased. This makes the
    reaction more spontaneous.
  • Voltage will then decrease if the concentration
    of the reactants is decreased or that of the
    products is increased. This makes the reaction
    less spontaneous.

26
The Nernst Equation
  • Offers a quantitative relationship between cell
    voltage concentration
  • E Eo - RT lnQ
  • nF
  • or at standard conditions (25oC)
  • E Eo - 0.0257 V lnQ
  • n

27
Interpreting Q
  • If Q gt 1 - concentration of the products are high
    so E lt Eo
  • (meaning lnQ is positive)
  • If Q lt 1 - concentration of the reactants are
    high so E gt Eo
  • (meaning lnQ is negative)
  • If Q 1 - reaction at standard conditions for
    cell voltage so E Eo
  • (meaning lnQ 0)

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Electrolytic Cells
  • An electrolytic cell is a non-spontaneous redox
    reaction that made to occur by pumping electrical
    energy into the system.
  • When carried out in an electrochemical cell this
    is referred to as electrolysis. This is the
    procedure used when electroplating. Electrons are
    pushed into the cathode and removing them from
    the anode.

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Quantitative Relationships
  • Quantitative relationships between the amount of
    electricity passed through an electrochemical
    cell
  • For the reaction Cu2 (aq) 2e- ? Cu (s)
  • 2 mol e- 1 mol Cu (s) 63.55 g Cu
  • Coloumb (C) the quantity of electrical charge
    (or electrical current).
  • 1 mol e- 9.648 x 104 C
  • Determining Current flow I q/t
  • Ampere (A) unit for the rate of current flow,
    (1 A 1 C/s)
  • Current (C) over time (s)
  • Joule (J) the amount of electrical energy, 1 J
    1 CV

34
Electrochemistry Stoichiometry
35
From left to right, Walther Nernst, Albert
Einstein, Max Planck, Robert Millikan, and Max
von Laue.
36
FRQ 1
  • It is observed that when silver metal is placed
    in aqueous thallium(I) fluoride, TlF, no reaction
    occurs. When the switch is closed in the cell,
    the voltage reading is 1.14 V.
  • (a) Write the reduction half-reaction that occurs
    in the cell.
  • (b) Write the equation for the overall reaction
    that occurs in the cell.
  • (c) Identify the anode in the cell. Justify your
    answer.
  • (d) On the diagram above, use an arrow to clearly
    indicate the direction of electron flow as the
    cell operates.
  • (e) Calculate the value of the standard reduction
    potential for the Tl/Tl half-reaction.
  • The standard reduction potential, E, of the
    reaction Pt2 2 e- ? Pt is 1.20 V.
  • (f) Assume that electrodes of pure Pt, Ag, and Ni
    are available as well as 1.00 M solutions of
    their salts.
  • Three different electrochemical cells can be
    constructed using these materials. Identify the
    two metals that when used to make an
    electrochemical cell would produce the cell with
    the largest voltage. Explain how you arrived at
    your answer.
  • (g) Predict whether Pt metal will react when it
    is placed in 1.00 M AgNO3(aq). Justify your
    answer.

37
FRQ 2
  • 2 H2(g) O2(g) ? 2 H2O(l)
  • In a hydrogen-oxygen fuel cell, energy is
    produced by the overall reaction represented
    above.
  • (a) When the fuel cell operates at 25C and 1.00
    atm for 78.0 minutes, 0.0746 mol of O2(g) is
    consumed. Calculate the volume of H2(g) consumed
    during the same time period. Express your answer
    in liters measured at 25C and 1.00 atm.
  • (b) Given that the fuel cell reaction takes place
    in an acidic medium,
  • (i) write the two half reactions that occur as
    the cell operates,
  • (ii) identify the half reaction that takes place
    at the cathode, and
  • (iii) determine the value of the standard
    potential, E, of the cell.
  • (c) Calculate the charge, in coulombs, that
    passes through the cell during the 78.0 minutes
    of operation as described in part (a).

38
FRQ 3
An external direct-current power supply is
connected to two platinum electrodes immersed in
a beaker containing 1.0 M CuSO4(aq) at 25C, as
shown in the diagram above. As the cell operates,
copper metal is deposited onto one electrode and
O2(g) is produced at the other electrode. The two
reduction half-reactions for the overall reaction
that occurs in the cell are shown in the table
below.
Half-Reaction E0(V)
O2(g) 4 H(aq) 4 e- ? 2 H2O(l) 1.23
Cu2(aq) 2 e- ? Cu(s) 0.34
(a) On the diagram, indicate the direction of
electron flow in the wire. (b) Write a balanced
net ionic equation for the electrolysis reaction
that occurs in the cell. (c) Predict the
algebraic sign of ?G for the reaction. Justify
your prediction. (d) Calculate the value of ?G
for the reaction. An electric current of
1.50 amps passes through the cell for 40.0
minutes. (e) Calculate the mass, in grams, of the
Cu(s) that is deposited on the electrode. (f)
Calculate the dry volume, in liters measured at
25C and 1.16 atm, of the O2(g) that is produced.
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