Free Nernst Equation Calculator

V
mol

E = E° − RT/zF × ln([red]/[ox])

R = 8.314 J/(K·mol) · F = 96,485.3 C/mol

Enter values above and the result will update automatically

The Nernst equation is a cornerstone of electrochemistry. This reduction potential calculator (also referred to as a cell potential calculator) applies the Nernst equation to determine the actual potential of a half‑cell or full‑cell reaction under any temperature and concentration conditions. It serves as a comprehensive electrochemistry calculator for students, researchers, and professionals who need quick and accurate results.

Reduction Potential and Standard Electrode Potential

Reduction potential (redox potential) indicates how strongly a chemical species tends to gain electrons and be reduced. A higher potential means a stronger tendency to be reduced, while a lower potential indicates a preference for oxidation. However, a high potential does not guarantee the reaction will occur; some activation energy is typically required. Because absolute potential values are hard to measure, potentials are always reported relative to a reference. The standard electrode potential (often called standard reduction potential) is measured with respect to the standard hydrogen electrode (SHE), which is arbitrarily assigned 0 V. Standard conditions include a temperature of 25 °C, unit activity for each ion, and a pressure of 1 bar for gases.

The Nernst Equation (Cell Potential Equation)

The Nernst equation relates the reduction potential EE to the standard electrode potential E0E₀, temperature TT, the number of electrons transferred zz, and the ratio of activities (or concentrations) of the reduced and oxidized species:

E=E0−RTzFln⁡[red][ox]E = E₀ - \frac{RT}{zF} \ln\frac{[\text{red}]}{[\text{ox}]}

Where:

  • EE – reduction potential under non‑standard conditions (V)
  • E0E₀ – standard electrode potential (V, relative to SHE)
  • RR – universal gas constant, 8.314 J/(K⋅mol)8.314\ \text{J/(K·mol)}
  • TT – absolute temperature (K)
  • zz – moles of electrons transferred in the balanced half‑ or full‑cell reaction
  • FF – Faraday constant, 96485.3 C/mol96485.3\ \text{C/mol}
  • [red][\text{red}] – activity (or molar concentration) of the species being reduced
  • [ox][\text{ox}] – activity (or molar concentration) of the species being oxidized

In many practical situations, concentrations can replace activities when the solution is dilute.

Worked Example

Consider the spontaneous redox reaction between magnesium and lead ions:

Oxidation (anode): Mg→Mg2++2e−\text{Mg} \rightarrow \text{Mg}^{2+} + 2e^-, Eox=+2.38 VE_\text{ox} = +2.38\ \text{V}
Reduction (cathode): Pb2++2e−→Pb\text{Pb}^{2+} + 2e^- \rightarrow \text{Pb}, Ered=−0.13 VE_\text{red} = -0.13\ \text{V}

Overall: Pb2+(aq)+Mg(s)→Mg2+(aq)+Pb(s)\text{Pb}^{2+}(aq) + \text{Mg}(s) \rightarrow \text{Mg}^{2+}(aq) + \text{Pb}(s)
Standard cell potential: E0=2.38 V+(−0.13 V)=2.25 VE₀ = 2.38\ \text{V} + (-0.13\ \text{V}) = 2.25\ \text{V}

Two electrons are transferred (z=2z = 2). The temperature is 25 °C (298.15 K). The concentration of Pb²⁺ is 0.200 M and that of Mg²⁺ is 0.020 M.

The reaction quotient for the net cell reaction is:

Q=[Mg2+][Pb2+]=0.0200.200=0.1Q = \frac{[\text{Mg}^{2+}]}{[\text{Pb}^{2+}]} = \frac{0.020}{0.200} = 0.1

The Nernst equation for the full cell then becomes:

E=E0−RTzFln⁡Q=2.25 V−(8.314 J/(K⋅mol))(298.15 K)(2)(96485.3 C/mol)ln⁡(0.1)=2.25 V−(0.01285 V)(−2.303)=2.25 V+0.0296 V=2.28 V\begin{aligned} E &= E₀ - \frac{RT}{zF} \ln Q \\ &= 2.25\ \text{V} - \frac{(8.314\ \text{J/(K·mol)})(298.15\ \text{K})}{(2)(96485.3\ \text{C/mol})} \ln(0.1) \\ &= 2.25\ \text{V} - (0.01285\ \text{V})(-2.303) \\ &= 2.25\ \text{V} + 0.0296\ \text{V} = 2.28\ \text{V} \end{aligned}

This calculated cell potential (2.28 V) is slightly higher than the standard value (2.25 V) because the concentration ratio is not 1. Using a dedicated electrochemistry calculator like this Nernst equation tool allows you to quickly evaluate the effect of different temperatures and concentrations on the cell potential.

FAQ

1. How do I calculate a cell potential using the Nernst equation?

Identify the standard electrode potentials (E₀) for the two half‑reactions, determine the moles of electrons transferred (z), and find the temperature (in Kelvin). Then evaluate the reaction quotient Q from the concentrations (or activities) of the species and plug everything into E = E₀ – (RT/zF) ln Q. For a full cell, E₀ is the sum of the half‑cell potentials.

2. What do R, T, z, and F stand for in the Nernst equation?

R is the universal gas constant (8.314 J/(K·mol)), T is the absolute temperature in Kelvin, z is the number of moles of electrons transferred, and F is the Faraday constant (96,485.3 C/mol).

3. Can I use concentrations instead of activities in the equation?

Yes, concentrations are often substituted for activities when the solution is dilute and the ionic strength is low. For highly accurate work or concentrated solutions, activities should be used.

4. In the worked example, why is the reaction quotient Q equal to [Mg²⁺]/[Pb²⁺]?

The net reaction is Pb²⁺(aq) + Mg(s) → Mg²⁺(aq) + Pb(s). Solids are omitted from Q because their activities are unity, so only the dissolved ions appear: Q = (activity of Mg²⁺)/(activity of Pb²⁺). The concentration ratio is then used as a close approximation.

How to Use

  1. Enter the standard reduction potential E° in volts.
  2. Set the temperature and choose the temperature unit.
  3. Enter the number of electrons transferred (z) in the reaction.
  4. Enter the activities (or concentrations) of the reduced and oxidized forms.
  5. Click Calculate to compute the reduction potential using the Nernst equation.