Model cathode, anode, overpotential, resistance, and temperature effects. Visualize voltage components instantly and export reports. Build clearer electrochemical calculations for study, testing, and planning.
Enter the anode value as the standard reduction potential of the reverse pair. Example: for water oxidation, use the O2/H2O reduction value.
| Parameter | Example Value | Meaning |
|---|---|---|
| Cathode E° | 0.00 V | Hydrogen evolution reference reduction potential. |
| Cathode n | 2 | Two electrons per H2 molecule. |
| Cathode Q | 1 | Standard-state example. |
| Anode E° | 1.23 V | O2/H2O reduction pair entered for the reverse oxidation side. |
| Anode n | 4 | Four electrons per O2 molecule. |
| Anode Q | 1 | Standard-state example. |
| Temperature | 25 °C | Room-temperature case. |
| Anode overpotential | 0.35 V | Kinetic loss at the anode. |
| Cathode overpotential | 0.20 V | Kinetic loss at the cathode. |
| Current | 10 A | Operating current. |
| Resistance | 0.08 Ω | Cell ohmic resistance. |
| Time | 2 h | Runtime for charge and energy estimates. |
| Faradaic efficiency | 95% | Useful current fraction. |
| Expected applied voltage | 2.58 V | 1.23 + 0.35 + 0.20 + 0.80. |
E = E° - (RT / nF) ln(Q)Vrev = Eanode,actual - Ecathode,actualVapplied = Vrev + ηanode + ηcathode + IR
Qcharge = I × tP = Vapplied × IEnergy = P × time
moles = (Q × FE) / (nF)mass = moles × molar mass.
Electrolysis voltage is the external cell voltage needed to force a nonspontaneous reaction. It includes the reversible thermodynamic requirement plus kinetic losses and resistive losses inside the cell.
Real cells need extra voltage to overcome activation barriers at electrodes and ohmic resistance in electrolyte, separator, contacts, and wiring. Those added terms are overpotential and IR drop.
Electrode tables usually list standard reduction potentials. Using the reverse-pair reduction value keeps the input consistent and lets the calculator build the required electrolysis voltage directly.
The reaction quotient adjusts each half-cell potential away from standard conditions through the Nernst equation. It captures concentration, pressure, and activity effects on the reversible voltage.
Overpotential is extra voltage lost at an electrode because reaction kinetics are not infinitely fast. Different materials, catalysts, surfaces, and current densities change its size.
IR drop is the voltage loss caused by current flowing through resistance. It rises with current and includes electrolyte, membrane, electrode, and connector resistance.
Yes. It uses Faraday’s law with your current, time, electron count, and Faradaic efficiency. Optional molar mass inputs convert theoretical moles into product mass.
Use Q = 1 when you want standard-state behavior or when you intentionally ignore concentration and pressure shifts. That makes the Nernst correction equal to zero.
Important Note: All the Calculators listed in this site are for educational purpose only and we do not guarentee the accuracy of results. Please do consult with other sources as well.