Potential step methods continued electrode

For measurement of R/Rq t, the potential step method is frequendy used the electrode potential is first set at a potential where no adsorption of the sample occurs and then stepped up to the second potential where adsorption does occur. The R/Rq t curve continues to be recorded until no further change in R/Rq takes place. 

As was mentioned in Sects. 2.8.1 and 2.8.2, application of the Laplace transform to the transient potential and current permits determination of the operational impedance. Such a method was initially introduced by Pilla [90-93] and applied to studies using mercury electrodes. Using a fast potentiostat a small potential step was applied, and both voltage and current transients were measured. Of course, because of the nonideal potentiostat response, the potential increase was not a rectangular step but occiured more slowly. Examples of the measured potential and current transients are shown in Fig. 3.6. Such data acquisition was extended to longer times and then extrapolated as the integration had to be continued to inlinity. 

Fig. 5.18 Potentiostatic methods (A) single-pulse method, (B), (C) double-pulse methods (B for an electrocrystallization study and C for the study of products of electrolysis during the first pulse), (D) potential-sweep voltammetry, (E) triangular pulse voltammetry, (F) a series of pulses for electrode preparation, (G) cyclic voltammetry (the last pulse is recorded), (H) d.c. polarography (the electrode potential during the drop-time is considered constant this fact is expressed by the step function of time—actually the potential increases continuously), (I) a.c. polarography and (J) pulse polarography...

Nanocarbons can also be deposited onto surfaces via electrochemistry, such as electrophoretic deposition described earlier. A method for one-step electrochemical layer-by-layer deposition of GO and PANI has been reported by Chen et al. [199]. A solution of GO and aniline was prepared and deposited onto a working electrode via cyclic voltammetry. GO was reduced on the surface when a potential of approx. -1 V (vs. SCE) was applied compared to the polymerization of aniline which occurred at approx. 0.7 V (vs. SCE). Repeated continuous scans between -1.4 to 9 V (vs. SCE) resulted in layer by layer deposition [199]. A slightly modified method has been reported by Li et al. who demonstrated a general method for electrochemical RGO hybridization by first reducing GO onto glassy carbon, copper, Ni foam, or graphene paper to form a porous RGO coating [223]. The porous RGO coated electrode could then be transferred to another electrolyte solution for electrochemical deposition, PANI hybridization was shown as an example [223]. 

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