Potentiostatic technique

Each of these two procedures can be varied by proceeding from a low to a high current density (or potential) or from a high to a low current density (or potential) the former is referred to as forward polarisation and the latter as reverse polarisation. Furthermore, there are a number of variations of the potentiostatic technique, and in the potentiokinetic method the pwtential of the electrode is made to vary continuously at a predetermined rate, the current being monitored on a recorder in the pulse method the electrode is given a pulse of potential and the current transient is determined by means of an oscilloscope. [Pg.107]

The potentiostatic technique has a number of variations and the potential may be increased or decreased incrementally, changed continuously at a predetermined rate (potential sweep) or applied as pulses of very short duration. The applications of the potentiostatic technique are considered in detail in Sections 1.4, 1.5 and 19.2, and will not be considered here. [Pg.1006]

The potentiostatic technique discussed here involves the polarisation of a metal electrode at a series of predetermined constant potentials. Potentio-stats have been used in analytical chemistry for some time Hickling was the first to describe a mechanically controlled instrument and Roberts was the first to describe an electronically controlled instrument. Greene has discussed manual instruments and basic instrument requirements. [Pg.1107]

The potentiostat is particularly useful in determining the behaviour of metals that show active-passive transition. Knowledge of the nature of passivity and the probable mechanisms involved has accumulated more rapidly since the introduction of the potentiostatic technique. Perhaps of more importance for the subject at hand are the practical implications of this method. We now have a tool which allows an operational definition of passivity and a means of determining the tendency of metals to become passive and resist corrosion under various conditions. [Pg.1110]

Another contribution of the potentiostatic technique to s.c.c. studies has been the report that cracking prevails essentially at two potential levels for metals showing an active-passive transition. These potentials are located near the top and bottom of the passive region. Along the same lines, Uhlig and his co-workers have determined critical ranges of potential for s.c.c. , although their theoretical interpretation differs from that of the other references cited. [Pg.1119]

Controlled-potential (potentiostatic) techniques deal with the study of charge-transfer processes at the electrode-solution interface, and are based on dynamic (no zero current) situations. Here, the electrode potential is being used to derive an electron-transfer reaction and the resultant current is measured. The role of the potential is analogous to that of the wavelength in optical measurements. Such a controllable parameter can be viewed as electron pressure, which forces the chemical species to gain or lose an electron (reduction or oxidation, respectively). [Pg.2]

Accordingly, the resulting current reflects the rate at which electrons move across the electrode-solution interface. Potentiostatic techniques can thus measure any chemical species that is electroactive, in other words, that can be made to reduce or oxidize. Knowledge of the reactivity of functional group in a given compound can be used to predict its electroactivity. Nonelectroactive compounds may also be detected in connection with indirect or derivatization procedures. [Pg.3]

For the individual types of transient measuring techniques, special names exist but their terminology lacks uniformity. The potentiostatic techniques where the time-dependent current variation is determined are often called chronoamperometric, and the galvanostatic techniques where the potential variation is determined are called chronopotentiometric. For the potentiodynamic method involving linear potential scans, the term voltammetry is used, but this term is often used for other transient methods as well. [Pg.200]

Controlled potential methods have been successfully applied to ion-selective electrodes. The term voltammetric ion-selective electrode (VISE) was suggested by Cammann [60], Senda and coworkers called electrodes placed under constant potential conditions amperometric ion-selective electrodes (AISE) [61, 62], Similarly to controlled current methods potentiostatic techniques help to overcome two major drawbacks of classic potentiometry. First, ISEs have a logarithmic response function, which makes them less sensitive to the small change in activity of the detected analyte. Second, an increased charge of the detected ions leads to the reduction of the response slope and, therefore, to the loss of sensitivity, especially in the case of large polyionic molecules. Due to the underlying response mechanism voltammetric ISEs yield a linear response function that is not as sensitive to the charge of the ion. [Pg.118]

Potentiostatic Transient Technique, In the potentiostatic technique the potential of the test electrode is controlled, while the current, the dependent variable, is measured as a function of time. The potential difference between the test electrode and the reference electrode is controlled by a potentiostat (Fig. 6.21). The input function, a constant potential, and the response function, i = f(t), are shown in Figure 6.22. [Pg.105]

Potentiodynamic Technique. Adsorption of methanol on Pt in acid solution was studied by Breiter and Gilman (3) using a potentiostatic technique. The anodic sweep, with a sweep rate of 800 V/s, was started at rest potential and extended to 2.0 V with respect to a hydrogen reference electrode in the same solution. As shown in Figure 10.8, the current was recorded as a function of potential (time) in the absence (curve A) and in the presence (curve B) of methanol. The increase in current in curve B is due to oxidation of the adsorbed methanol on the platinum electrode. Thus, shaded area 2 minus shaded area 1 (Fig. 10.8) yields the change 2m (C/cm ) required for oxidation of the adsorbed methanol ... [Pg.184]

The homogeneous catalysis method is suitable to measure rate constants over a very wide range, up to the diffusion limit. The lower limit is determined by interferences, such as convection, which occur at very slow scan rates. It is our experience that, unless special precautions are taken, scan rates below lOOmV/s result in significant deviations from a purely diffusion-controlled voltammetric wave. For small values of rate constants (down to 10 s ), other potentiostatic techniques are best suited, such as chronoamperometry at a rotating disk electrode UV dip probe and stopped-flow UV-vis techniques. ... [Pg.97]

Whereas in earlier work it was usual to conduct synthetic reactions of this nature under constant current conditions, in recent years greater control and understanding of the systems have been achieved by employing potentiostatic techniques in which the potential of the working electrode (anode) is regulated precisely with respect to a third, reference electrode (e.g., Ag/Ag+ or saturated calomel, SCE). [Pg.199]

Potentiostatic techniques, 787, 1115, 1118 and impurities on electrodes. 1120 potential interval measurements, 1121 p-polarized light, 802 Potentiodynamic techniques, 1423, 1438 vs. potentiostatic techniques, 1426 Potentiostatic transients, 1414 difficulties in, 1415 double layer charging, 1416 radicals in, 1416 IR drop in, 1416 Prandtl layer, 1228... [Pg.47]

In terms of the earlier material, this technique is nearest to the potentiostatic technique, but because here the potential is made to vary linearly with time (i.e., it is not static), the more appropriate name ispotentiodynaniic. As far as the electrode, cell, etc., are concerned, one has the same setup as with potentiostatic transients the difference is that instead of being fixed at a given value while the ip is observed, the potential is made to change at a constant rate over a chosen potential range. The range of acceptable values for the sweep rate is something to be discussed in detail later, but it may be stated now that a typical value is 10 mV s ... [Pg.706]

A. A. Pilla, Influence of the Faradaic Process on Nonfaradaic Resistance Compensation in Potentiostatic Techniques, J. Electrochem. Soc. 118 102 (1971). [Pg.234]

Figure 3 The experimental setup window showing the potentiostatic technique option.

Using the POTENTIOSTATIC technique, you will sequence through a series of increasing applied potentials while monitoring the current. [Pg.379]

Figure 31 PARC 352 SoftCorr HI Potentiostatic technique combo box.

Potentiostatic techniques — In the strict sense, techniques in which the -> electrode potential is kept constant with the help of a potentiostat. The term, however, is also used for techniques in which the electrode potential is linearly or stepwise changed using a potentiostat. [Pg.545]

Linear potential sweep is a potentiostatic technique, in the sense that the potential is the externally controlled parameter. The potential is changed at a constant rate... [Pg.522]

Potentiostatic techniques developed later gave more Intelligible results. The simplest potential-pulse technique, first used by Kaischew, Scheludko, and Bliznakov... [Pg.174]

For the detection of dopamine, controlled-potential (potentiostatic) techniques, which are concerned with the study of charge transfer processes at the electrode-solution interface, are favored due to a number of advantages. These include high sensitivity, selectivity towards electroactive species, wide linear range, portability and low cost of instrumentation, speciation capability and a wide range of electrodes which allow assays of unusual environments [29]. [Pg.321]

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