Galvanic (Voltaic) Cell
A **galvanic (voltaic) cell** harnesses a spontaneous redox reaction to push electrons through an external circuit. This page shows a schematic **two-beaker** layout with a **salt bridge**, metal electrodes, and a **voltmeter** on the wire. You choose two metal ion / metal couples (standard reduction potentials E° vs SHE are rounded textbook values). The model automatically assigns **anode** (oxidation, lower E° couple) on the **left** and **cathode** (reduction, higher E° couple) on the **right** so the diagram always matches spontaneous electron flow left → right in the wire. Ion concentrations in each half-cell feed the **overall reaction quotient Q** for the balanced cell reaction (including correct stoichiometric powers when n differs between halves, e.g. Zn with Ag⁺). The **Nernst equation** E_cell = E°cell − (RT/nF) ln Q updates the displayed potential; temperature is adjustable. **Electron dots** animate along the external path when E_cell ≥ 0 and slow or reverse for non-spontaneous combinations. Junction potentials, activity coefficients, complex speciation, and concentration overpotential are omitted—concentrations stand in for activities—so numbers are for **conceptual practice** next to the standalone Nernst equation lab.
Who it's for: High school and introductory college chemistry alongside redox, standard potentials, and the Nernst equation; bridges formula practice to a whole-cell picture.
Key terms
- Galvanic cell
- Anode and cathode
- Standard reduction potential
- Salt bridge
- Cell potential
- Nernst equation
- Reaction quotient
- Faraday constant
How it works
A **voltaic (galvanic) cell** converts spontaneous redox chemistry into electrical work. This page sketches **two beakers**, a **salt bridge**, and an **external wire** with a voltmeter. Standard reduction potentials decide **which side oxidizes**; the **Nernst equation** updates **E_cell** when ion concentrations depart from 1 M.
Key equations
Frequently asked questions
- Why does the left side always show the anode?
- The drawing is reorganized after reading your two half-cell choices so that oxidation (lower E° as a reduction couple) is always on the left and reduction on the right. That matches the usual textbook sketch of electron travel through the external wire from anode to cathode.
- How is Q built when silver (Ag⁺/Ag, one electron) is paired with zinc (two electrons)?
- The overall reaction is balanced with the least common multiple of the half-reaction electron counts. For Zn + 2Ag⁺ → Zn²⁺ + 2Ag, n = 2 and Q = [Zn²⁺]/[Ag⁺]² when solids are omitted from Q.
- Why might my voltage disagree with a measured cell?
- Real cells have junction potentials at the salt bridge, non-unity activity coefficients, and often side reactions or passivation. The simulator uses 1 M standard states, idealized E° values, and concentrations as activities.
- What if both half-cells are the same metal?
- Then E°cell = 0 and, with identical treatment of both sides, E_cell = 0—the cartoon represents no net galvanic drive.
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