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Electrochemical Characterization of a Novel Salen-Type Modified Electrode
Author(s) -
Miguel VilasBoas,
Cristina Freire,
Baltazar de Castro,
A. Robert Hillman
Publication year - 1998
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp982160r
Subject(s) - chronoamperometry , horizontal scan rate , cyclic voltammetry , electrochemistry , materials science , diffusion , counterion , electrode , redox , chemical engineering , analytical chemistry (journal) , inorganic chemistry , chemistry , organic chemistry , thermodynamics , ion , engineering , physics
The nickel(II) complex with H2saltMe, a N2O2 Schiff base ligand derived from salicylaldehyde, was oxidatively electropolymerized on Pt electrodes in CH3CN/0.1 mol dm-3 tetraethylammonium perchlorate (TEAP) to generate polymer films that exhibit reversible oxidative electrochemical behavior in a wide potential range (0.0−1.3 V), high conductivity, and stability/durability. The films of poly[Ni(saltMe)] can be made to exhibit the three regimes of charge transport behavior by manipulation of the film thickness and the experimental time scale. Films prepared by a small number of potential cycles show thin-layer/surface-type cyclic voltammetry behavior in the scan rate range used. Thicker polymers exhibit a changeover from this thin-layer regime to diffusion control at a critical scan rate that depends on film thickness. In chronoamperometry experiments a transition from semiinfinite diffusion to finite diffusion conditions was observed at longer times following the potential step.Values of D1/2C for the secon...

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