Electrochemistry and Galvanic Cells

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Vocabulary flashcards covering electrochemistry, galvanic cells, cell potential calculations, free energy relationships, concentration cells, battery capacity, and modern 3D battery architectures.

16 Terms

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Galvanic Cell

An electrochemical cell in which spontaneous reduction and oxidation reactions take place in separate locations to harness electron transfer and generate electricity.

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Cathode

The electrode where reduction takes place (gaining electrons, e−e^-), corresponding to the half-reaction with the higher standard reduction potential (E∘E^\circ).

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Anode

The electrode where oxidation takes place (losing electrons, e−e^-), corresponding to the half-reaction with the lower standard reduction potential (E∘E^\circ).

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Salt Bridge

A U-tube containing an electrolyte solution (such as K2SO4\text{K}_2\text{SO}_4 or KNO3\text{KNO}_3) that maintains electrical neutrality between two half-cells by allowing cations to flow toward the cathode and anions to flow toward the anode.

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

The equation used to determine overall cell potential: Ecell∘=Ered∘−Eox∘E^\circ_{\text{cell}} = E^\circ_{\text{red}} - E^\circ_{\text{ox}} (or Ecell∘=Ecat∘−Ean∘E^\circ_{\text{cell}} = E^\circ_{\text{cat}} - E^\circ_{\text{an}}), where the minus sign automatically accounts for the reversed oxidation reaction.

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Standard Free Energy Change (ΔG∘\Delta G^\circ)

A thermodynamic parameter calculated by ΔG∘=−nFE∘\Delta G^\circ = -nFE^\circ, where a negative value indicates a spontaneous, product-favored process.

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Faraday's Constant (FF)

A constant value given as 96.5 kJ/(V×mol e−)96.5\,\text{kJ}/(\text{V}\times\text{mol }e^-), representing electric charge per mole of electrons.

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Product-Favored Criteria

The thermodynamic conditions required for a spontaneous forward electrochemical reaction, defined by Ecell∘>0E^\circ_{\text{cell}} > 0 and/or ΔG∘<0\Delta G^\circ < 0.

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Spectator Ions

Ions present in an electrochemical cell's electrolyte solution (such as SO42−\text{SO}_4^{2-} or NO3−\text{NO}_3^-) that maintain charge balance without undergoing oxidation or reduction.

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Concentration Cell

A galvanic cell in which both half-cells contain identical electrodes and chemical species (Ecell∘=0 VE^\circ_{\text{cell}} = 0\,\text{V} under standard conditions), driven to produce voltage solely by a difference in ion concentrations until equilibrium is reached.

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Battery "Death"

The termination of galvanic cell function occurring when at least one reactant electrode and/or reactant solution is depleted.

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Battery Capacity

The total amount of work a battery can perform, which increases with a greater quantity of reactants ("more reactants, more work") even when different battery sizes (AAA, AA, C, D) share identical chemistry and voltage (1.5 V1.5\,\text{V}).

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<p>3D Battery</p>

3D Battery

An advanced architectural design with interdigitated cathode and anode structures surrounded by electrolyte, designed to charge faster and last longer.

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<p>Prof Amy Prieto</p>

Prof Amy Prieto

A researcher at Colorado State University noted for developing advanced 3D battery electrodes that charge faster and last longer.

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<p>Zinc-Copper Cell Reaction</p>

Zinc-Copper Cell Reaction

The spontaneous galvanic reaction Zn(s)+Cu2+(aq)→Zn2+(aq)+Cu(s)\text{Zn}(s) + \text{Cu}^{2+}(aq) \rightarrow \text{Zn}^{2+}(aq) + \text{Cu}(s) with Ecell∘=+1.1 VE^\circ_{\text{cell}} = +1.1\,\text{V} and ΔG∘=−212 kJ\Delta G^\circ = -212\,\text{kJ}.

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Lithium Cobalt Oxide Reaction

The spontaneous vehicle-powering reaction LiC6(s)+CoO2(s)→6C(s)+LiCoO2(s)\text{LiC}_6(s) + \text{CoO}_2(s) \rightarrow 6\text{C}(s) + \text{LiCoO}_2(s) with a calculated standard cell potential of Ecell∘=+3.85 VE^\circ_{\text{cell}} = +3.85\,\text{V}.