0000000000429347
AUTHOR
A. Roig
Identification of electroactive sites in Prussian Yellow films
Abstract Prussian Blue films were electrogenerated on the surface of the transparent ITO electrodes. The electrochemical oxidation to the Prussian Yellow form was investigated by means of in situ voltammetry and vis–NIR spectroscopic techniques. Changes of the whole spectra between 400 and 950 nm were analyzed and three characteristic wavelengths were selected to in situ follow the electrochemical changes of the films. Voltammetric peaks and absorbance derivative curves at these three wavelengths were deconvoluted and were interpreted such as the overlapping of different electrochemical processes. The correlation between these overlapped processes has allowed proposing three different elect…
Voltammetric behavior of berenil.
Abstract Berenil is reduced on mercury drops electrode in buffered aqueous media. The reduction of —N=N— group is controlled by diffusion. Polarographie waves are of analytical usefulness. The hydrogen discharge is favored by the basic centers of the molecule in Co(ll)/ammonia-buffered media.
Apparent activation energies and apparent frequency factor in polarographic waves of paludrine-Zn(II)
Abstract Arrhenius and Vlcek plots of ac 1 and dp polarograms of paludrine-Zn complexes are tested in order to understand the apparent activation energies and pre-exponential factor, and their dependence on the potential. These empirical treatments are useful for obtaining information about the energetic contributions of the elemental processes associated with the Zn(II) and paludrine ligands in the overall mechanism of reduction of the complex 2:1 on the mercury interface.
Anodic Dissolution of Nickel across Two Consecutive Electron Transfers
The analysis of the electrochemical quartz crystal microbalance and electrochemical impedance spectroscopy results are consistent with a nickel electrodissolution process limited by the passage of Ni(I) to Ni(II), when chloride ions are present in the acid sulfate medium, or by the passage of Ni(II) to Ni 2+ in solution, in absence of chloride. This interpretation allows an explanation of the potential evolution of Fdm/dQ values in both experimental conditions by assuming the formation of a new phase on the electrode surface with a gel-like structure placed between the metal and the solution. Ni(I) surface concentration is calculated from the instantaneous mass/charge Fdm/dQ values.