Abstract
The deactivation of nickel hydroxide films after prolonged storage times without use was studied. This
study was carried out in the context of the Rotating Disc Electrode Voltammetry (RDEV) and
Electrochemical Impedance Spectroscopy (EIS) when the nickel hydroxide film contacts an electroactive
solution and a redox reaction occurs at the Au-Ni(OH)2|electrolyte interface. Deferasirox (4-(3,5-bis(2-
hydroxyphenyl)-1,2,4-triazol-1-yl) benzoic acid) was employed as redox species in solution. Limiting
currents vs. electrode rotation rate dependences allowed one to obtain variation of the charge transport rate
on the storage time. EIS was employed to obtain a more complete series of charge-transport parameters,
that is, electron and ion diffusion coefficients and different interfacial resistances related to the gold/nickel
hydroxide and nickel hydroxide/solution interfaces.
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