A model of reversible and quasi-reversible electrode reaction of dissolved redox couple is developed for the staircase voltammetry and the twin electrode thin layer cell. It is assumed that the neutral molecule is oxidized to a monovalent cation. The calculations were performed for the absence of supporting electrolyte and for its various concentrations. The influence of migration of cations and of IRΩ drop on the peak currents and peak potentials was investigated. Also, the kinetically controlled electrode reactions were simulated. These reactions can be distinguished from the reactions influenced by the resistance in the solution
Cyclic staircase voltammograms of a simple, reversible oxidation on the rotating disk electrode is a...
The theory of cyclic voltammetry of ion transfer-electron transfer coupled reactions in a thick orga...
Many enzymes that contain quinone moieties or polyvalent metal ions (V, W, Mo, Mn) as redox active c...
A model of reversible and quasi-reversible electrode reaction of dissolved redox couple is developed...
Redox processes in which oxidation and reduction take place from different state are important syste...
The voltammetric response of electrodes coated with a redox-active monolayer is computed by finite e...
A continuum-model approach, analogous to porous electrode theory, was applied to a thin-layer cell o...
When self assembled monolayers (SAMs) containing redox centres behave ideally it is a relatively str...
Redox cycling between two electrodes separated by a narrow gap allows dramatic amplification of the ...
Chronoamperometric transients are recorded in different quantities of supporting electrolyte, from f...
Abstract The performances of reverse electrodialysis depend on several factors, including the nature...
Electrode transformation of many metal ions, drugs, and physiologically relevant compounds from wate...
Thin ion-selective membrane films deposited on solid electrode substrate are useful tools to study i...
Protein-film voltammetry is recognized as a simple but useful technique that can provide access to t...
Extracting quantitative kinetic information from linear-sweep voltammograms (LSV) on porous electrod...
Cyclic staircase voltammograms of a simple, reversible oxidation on the rotating disk electrode is a...
The theory of cyclic voltammetry of ion transfer-electron transfer coupled reactions in a thick orga...
Many enzymes that contain quinone moieties or polyvalent metal ions (V, W, Mo, Mn) as redox active c...
A model of reversible and quasi-reversible electrode reaction of dissolved redox couple is developed...
Redox processes in which oxidation and reduction take place from different state are important syste...
The voltammetric response of electrodes coated with a redox-active monolayer is computed by finite e...
A continuum-model approach, analogous to porous electrode theory, was applied to a thin-layer cell o...
When self assembled monolayers (SAMs) containing redox centres behave ideally it is a relatively str...
Redox cycling between two electrodes separated by a narrow gap allows dramatic amplification of the ...
Chronoamperometric transients are recorded in different quantities of supporting electrolyte, from f...
Abstract The performances of reverse electrodialysis depend on several factors, including the nature...
Electrode transformation of many metal ions, drugs, and physiologically relevant compounds from wate...
Thin ion-selective membrane films deposited on solid electrode substrate are useful tools to study i...
Protein-film voltammetry is recognized as a simple but useful technique that can provide access to t...
Extracting quantitative kinetic information from linear-sweep voltammograms (LSV) on porous electrod...
Cyclic staircase voltammograms of a simple, reversible oxidation on the rotating disk electrode is a...
The theory of cyclic voltammetry of ion transfer-electron transfer coupled reactions in a thick orga...
Many enzymes that contain quinone moieties or polyvalent metal ions (V, W, Mo, Mn) as redox active c...