Reaction mechanisms of high-rate copper electrochemical machining in chloride and sulfate electrolytes

The electrochemical dissolution behavior of copper in sodium chloride and sodium sulfate electrolytes is analyzed mainly by measuring polarization curves. The nature and the influence of the surface film formed at the limiting current density plateau, on the reaction mechanism and etching behavior were examined. For high current densities, novel complexation mechanisms for the dissolution were assumed. These “Solvo-Chlorination” and “Solvo-Sulfatization” mechanisms were similar to the “Solvo-Nitration” mechanism that has recently been postulated for nitrate electrolytes. Differences in the limiting current density and the re-rise voltage (15–35 V in NaCl, 35 V in Na2SO4) were strongly connected to the properties of the surface film and the valence of dissolution. The dissolution mechanism of copper during high-rate electrochemical machining in chloride and sulfate electrolytes is investigated mainly by polarization studies. A similar change in reaction mechanism as postulated for nitrate electrolytes including the formed surface films can be assumed. However, the nature of the surface films differs. Institute Twitter/X account: @Fraunhofer ISE.

Authors

Institutions

Publication Details

Journal
Journal of Applied Electrochemistry
Published
2026-02-01
DOI
https://doi.org/10.1007/s10800-025-02398-8
Primary Topic
Electrodeposition and Electroless Coatings
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Reaction mechanisms of high-rate copper electrochemical machining in chloride and sulfate electrolytes

Ingo Krossing, Lasse Rieck, Leonie Jakob, Jonas Bartsch
Journal of Applied Electrochemistry
Electrodeposition and Electroless Coatings
article

Reaction mechanisms of high-rate copper electrochemical machining in chloride and sulfate electrolytes

Ingo Krossing, Lasse Rieck, Leonie Jakob, Jonas Bartsch
article en

Abstract

The electrochemical dissolution behavior of copper in sodium chloride and sodium sulfate electrolytes is analyzed mainly by measuring polarization curves. The nature and the influence of the surface film formed at the limiting current density plateau, on the reaction mechanism and etching behavior were examined. For high current densities, novel complexation mechanisms for the dissolution were assumed. These “Solvo-Chlorination” and “Solvo-Sulfatization” mechanisms were similar to the “Solvo-Nitration” mechanism that has recently been postulated for nitrate electrolytes. Differences in the limiting current density and the re-rise voltage (15–35 V in NaCl, 35 V in Na2SO4) were strongly connected to the properties of the surface film and the valence of dissolution. The dissolution mechanism of copper during high-rate electrochemical machining in chloride and sulfate electrolytes is investigated mainly by polarization studies. A similar change in reaction mechanism as postulated for nitrate electrolytes including the formed surface films can be assumed. However, the nature of the surface films differs. Institute Twitter/X account: @Fraunhofer ISE.

Journal of Applied ElectrochemistryVol. 56(3)
University of Freiburg (DE), Fraunhofer Institute for Solar Energy Systems (DE)
Clean water and sanitation
Openalex Percentile: Top 70%
Electrodeposition and Electroless Coatings
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Reaction mechanisms of high-rate copper electrochemical machining in chloride and sulfate electrolytes — Ingo Krossing, Lasse Rieck, et al. · Journal of Applied Electrochemistry (2026) | TGRS Research Map | TGRS