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Rotating ring-disk electrode transients

In the non-steady state, changes of stoichiometry in the bulk or at the oxide surface can be detected by comparison of transient total and partial ionic currents [32], Because of the stability of the surface charge at oxide electrodes at a given pH, oxidation of oxide surface cations under applied potential would produce simultaneous injection of protons into the solution or uptake of hydroxide ions by the surface, resulting in ionic transient currents [10]. It has also been observed that, after the applied potential is removed from the oxide electrode, the surface composition equilibrates slowly with the electrolyte, and proton (or hydroxide ion) fluxes across the Helmholtz layer can be detected with the rotating ring disk electrode in the potentiometric-pH mode [47]. This pseudo-capacitive process would also result in a drift of the electrode potential, but its interpretation may be difficult if the relative relaxation of the potential distribution in the oxide space charge and across the Helmholtz double layer is not known [48]. [Pg.256]

Prater KB, Bard AJ (1970) Rotating ring-disk electrodes. 1. Fundamentals of the digital simulation approach. Disk and ring transients and collection efficiencies. J Electrochem Soc 117 207. [Pg.222]

Although a major advantage of rotating disk electrode techniques, compared to stationary electrode methods, is the ability to make measurements at steady state without the need to consider the time of electrolysis, the observation of current transients at the disk or ring following a potential step can sometimes be of use in understanding an electrochemical system. For example the adsorption of a component. [Pg.353]


See other pages where Rotating ring-disk electrode transients is mentioned: [Pg.261]    [Pg.810]    [Pg.121]    [Pg.142]    [Pg.6459]    [Pg.810]    [Pg.224]    [Pg.6458]    [Pg.285]    [Pg.4430]    [Pg.5557]    [Pg.261]    [Pg.66]    [Pg.256]    [Pg.266]    [Pg.92]    [Pg.148]    [Pg.197]    [Pg.238]    [Pg.646]   
See also in sourсe #XX -- [ Pg.355 , Pg.356 ]




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