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However, please VERIFY all results on your own, as the level of completion of this item is NOT CONFIRMED.
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This online calculator is currently under heavy development. It may or it may NOT work correctly.
You CAN try to use it. You CAN even get the proper results.
However, please VERIFY all results on your own, as the level of completion of this item is NOT CONFIRMED.
Feel free to send any ideas and comments !
Electrodes overpotential [V]#
Electrode / secreted substance | Al | Zn | Cr | Fe | Cd | Ni | Sn | Pb | Bi | Cu | Ag | Hg | Pt | C |
H2 acid environment | 0.8 | 0.7 | 0.5 | 0.5 | 1.2 | 0.4 | 1 | 1.3 | 0.8 | 0.6 | 0.4 | 1.2 | 0.1 | 0.5 |
H2 alkaline environment | 0.4 | 0.4 | - | 0.2 | - | 0.4 | 0.8 | 0.9 | 0.5 | - | - | 1.3 | 0.1 | - |
O2 | - | - | - | 0.25 | 0.4 | 0.1 | - | 0.3 | - | 0.2 | 0.4 | - | 0.4 | 0.3 |
Zn | - | 0.2 | - | - | 0.55 | - | - | - | - | 0.4 | - | - | 0.5 | - |
Cr | - | - | 0.6 | - | - | - | - | - | - | - | - | - | - | - |
Fe | - | - | - | 0.6 | - | - | - | - | - | - | - | - | - | - |
Cd | - | - | - | - | 0.2 | - | - | 0.35 | - | 0.35 | - | - | 0.35 | - |
Co | - | - | - | - | - | - | - | - | - | - | - | - | 0.3 | - |
Ni | - | - | - | - | - | 0.6 | - | - | - | - | - | 0.6 | - | - |
Sn | - | - | - | - | - | - | 0.2 | 0.3 | - | 0.3 | - | - | - | - |
Pb | - | - | - | - | - | - | - | 0.2 | 0.12 | 0.02 | - | - | - | - |
Bi | - | - | - | - | - | - | - | 0.2 | 0.35 | - | - | - | - | - |
Cu | - | - | - | - | - | - | - | - | 0.2 | - | - | - | 0.3 | - |
Ag | - | - | - | - | - | - | - | - | - | - | 0.2 | - | 0.8 | - |
Some facts#
- Overpotential is a difference between the potential of the electrode polarized by the flow of electric current and its potential in the equilibrium state.where:
- - overpotential of electrode,
- - potential of the electrode in a polarized state,
- - electrode potential in the equilibrium state.
- - overpotential of electrode,
- Overpotential is the polarization measure of the electrode.
- Overpotential is measured in volts (V).
- The author of the overpotential concept is W.A. Caspari. This concept appeared for the first time in 1899.
- The total overvoltage on the electrode consists of partial overvoltages:
where:
- - resistive overvoltage, related to the potential drop across the electrode-solution interface,
- - pseudo-resistance overvoltage, associated with the resistance of the electrolyte layer separating the test electrode and the reference electrode,
- - activation overvoltage, associated with an additional expenditure of electric potential to overcome the activation energy of the electrode reaction,
- - concentration overvoltage, associated with additional electrical work associated with changes in concentrations of electroactive substances in the immediate vicinity of a polarized electrode.
- - resistive overvoltage, related to the potential drop across the electrode-solution interface,
- Concentration overpotential can be calculated using Nernst equation:
where:
- – depolarizer activity at the surface of a polarized electrode,
- – the activity of the depolarizer in a state of equilibrium,
- – number of electrons transferred in the transition reaction,
- – gas constant,
- – absolute temperature in kelvins,
- – Faraday's constant.
- – depolarizer activity at the surface of a polarized electrode,
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