Calculation approach for current–potential behaviour during pulse electrodeposition based on double-layer characteristics

Abstract

This paper introduces a phenomenological calculation approach for the electrolytic pulse deposition of nickel under high polarisation based on an equivalent electrical circuit. In a quasistationary state of the deposition, the electrolyte resistance and double layer parameters are identified by electrochemical impedance spectroscopy and galvanostatic polarisation. The charge-transfer resistance of both the anodic and cathodic electrode double layer is inversely proportional to the current density. This means the overpotentials over the electrode double layers are independent of the current density. For short pulse on-times and off-times (up to 10 ms), the behaviour of the electrolytic cell is mainly determined by the double layer characteristics and the calculation approach therefore allows the prediction of the current-potential behaviour during pulse deposition under high polarisation. For larger pulse widths, the time-dependent evolution of the overpotentials occurring at the electrode/electrolyte interface becomes a determining factor for the cell potential.

Co-deposition behavior of alumina nanoparticles and properties of Ni-Al2 O3 nanocomposite coatings

“…, the increase in current density leads to a decline in charge transfer resistance, which behaves reciprocally to the current density. The charge transfer resistance and the cathode double layer are inversely proportional to the current density as explained in detail in . This inverse proportional relation between current density and charge transfer resistance, which was also found for high polarization in for a nickel sulfate electrolyte, leads to an interesting prediction concerning the system's behavior under high polarization.…”