Electrochemical Cell Potentials and Nernst Equation

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Description and Tags

Vocabulary terms and definitions covering the half-reactions, Nernst equation calculations, and chemical behavior of the provided electrochemical cell.

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<p>Electrochemical Cell Setup</p>

Electrochemical Cell Setup

A galvanic cell apparatus consisting of compartment A (1 L1\,\text{L} of 0.05 M H2SO40.05\,\text{M}\ H_2SO_4 with a Pt\text{Pt} electrode and 1 atm H21\,\text{atm}\ H_2 gas) and compartment B (1 L1\,\text{L} of 0.01 M AgNO30.01\,\text{M}\ AgNO_3 with a Pd\text{Pd} electrode) connected via a salt bridge and voltmeter.

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Anode Half-Reaction (Compartment A)

The oxidation process occurring at the Pt\text{Pt} electrode: H2(g)→2H+(aq)+2e−H_2(g) \rightarrow 2H^+(aq) + 2e^-, with a standard reduction potential of E∘=0.00 VE^\circ = 0.00\,\text{V}.

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Cathode Half-Reaction (Compartment B)

The reduction process occurring in compartment B: Ag+(aq)+e−→Ag(s)Ag^+(aq) + e^- \rightarrow Ag(s), with a standard reduction potential of E∘=+0.80 VE^\circ = +0.80\,\text{V}.

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Overall Cell Reaction

The complete balanced redox reaction: H2(g)+2Ag+(aq)→2H+(aq)+2Ag(s)H_2(g) + 2Ag^+(aq) \rightarrow 2H^+(aq) + 2Ag(s), transferring n=2n = 2 moles of electrons.

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Standard Cell Potential (Ecell∘E^\circ_{\text{cell}})

The standard electromotive force calculated as Ecathode∘−Eanode∘=+0.80 V−0.00 V=+0.80 VE^\circ_{\text{cathode}} - E^\circ_{\text{anode}} = +0.80\,\text{V} - 0.00\,\text{V} = +0.80\,\text{V}.

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Reaction Quotient (QQ)

The ratio of concentrations and partial pressures defined by Q=[H+]2[Ag+]2⋅PH2=(0.10 M)2(0.01 M)2⋅1 atm=102Q = \frac{[H^+]^2}{[Ag^+]^2 \cdot P_{H_2}} = \frac{(0.10\,\text{M})^2}{(0.01\,\text{M})^2 \cdot 1\,\text{atm}} = 10^2.

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Nernst Equation (Specified Form)

The non-standard potential formula given as Ecell=Ecell∘−0.06nlog⁡(Q)E_{\text{cell}} = E^\circ_{\text{cell}} - \frac{0.06}{n} \log(Q).

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Initial Cell Potential (EcellE_{\text{cell}})

The non-standard voltage of the cell under the specified initial conditions, calculated as 0.80 V−0.062log⁡(102)=0.74 V0.80\,\text{V} - \frac{0.06}{2} \log(10^2) = 0.74\,\text{V}.

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Compartment A pH Trend

The pH of the solution in compartment A decreases over time because the continuous oxidation of H2(g)H_2(g) generates H+(aq)H^+(aq) ions, increasing their concentration.

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Effect of Adding Pd(NO3)2Pd(NO_3)_2 to Compartment B

Dissolving Pd(NO3)2Pd(NO_3)_2 introduces Pd2+(aq)Pd^{2+}(aq), which has a higher reduction potential (E∘=+0.95 VE^\circ = +0.95\,\text{V}) than Ag+Ag^+ (E∘=+0.80 VE^\circ = +0.80\,\text{V}), altering the reduction half-reaction and changing the initial cell potential.