Potential-scanning techniques

On the one hand, the Ru presence helps the oxidation of the last and strongest adsorbed intermediate, the carbon monoxide. Ru helps the bifunctional mechanism because the formation of oxygenated species (Reaction (2.6)) takes place at lower potentials than on Pt [33]. However, Reaction (2.6) has slower kinetics on Ru than on Pt as proven by electrochemical impedance spectroscopy [34]. For this reason, the currents for Pt-Ru in potential scan techniques are larger than for Pt below 0.65 V, but become smaller above 0.65 V [34]. 

The widespread use of large-amplitude relaxation techniques in the investigations of anodic organic oxidations, requires further comment on the value of these methods. Reinmuth divided these techniques into three classes based on the types of applications quantitative kinetic studies, qualitative kinetic studies, and analytical studies. We are not concerned here with the analytical applications. For studies in kinetics, controlled-potential techniques, particularly linear-potential scan, in either single sweep or in cycles, and to some extent chronopotentiometry, have been primarily employed. Chronopotentiometry has been successfully utilized in the study of transient reactions, e.g., the reaction of CO with platinum oxide or the reaction of oxalic acid with platinum oxide, and the study of simple charge-transfer reactions with linear diffusion (cf. Refs. 159-161). However, since the general application of chronopotentiometry is severely limited for the study of anodic organic oxidations, as commented previously, this technique will not be further discussed. The quantitative analysis of data obtained by linear potential scan techniques is complicated because the form of theoretical results even for the simplest cases, requires the use of computers and consequently very little quantitative kinetic information has been obtained. This... 

Sensitivity In many voltammetric experiments, sensitivity can be improved by adjusting the experimental conditions. For example, in stripping voltammetry, sensitivity is improved by increasing the deposition time, by increasing the rate of the linear potential scan, or by using a differential-pulse technique. One reason for the popularity of potential pulse techniques is an increase in current relative to that obtained with a linear potential scan. 

The selection of the pulse amplitude and potential scan rate usually requires a trade-off among sensitivity, resolution, and speed. For example, larger pulse amplitudes result in larger and broader peaks. Pulse amplitudes of 25-50 mV, coupled with a 5 mV s 1 scan rate, are commonly employed. Irreversible redox systems result in lower and broader current peaks (i.e., inferior sensitivity and resolution) compared with those predicted for reversible systems (6). In addition to improvements in sensitivity and resolution, the technique can provide information about the chemical form in which the analyte appears (oxidation states, complexa-tion, etc.). 

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. 

The first version of a polarographic technique was put forward in 1922 by the Czech scientist Jaroslav Heyrovsky. Classsical polarography is the measurement of quasisteady-state polarization curves with linear potential scans applied to the DME sufficiently slowly (v between 1 and 20mV/s), so that within the lifetime, of an individual drop, the potential would not change by more than 3 to 5 mV. With special instruments (polarographs), one can record the resulting 7 vs. E curves (polaro-grams) automatically. 

Rapid-Scan Corrosion Behavior Diagram (CRD) Basically, all the same equipment used in the conductance of an ASTM G5 slow-scan polarization study is used for rapid-scan CBDs (that is, a standard test cell, potentiostat, voltmeters, log converters, X-Y recorders, and electronic potential scanning devices). The differences are in technique the slow scan is run at a potential sweep rate of about 0.6 V/h the rapid-scan CBDs at about 50 V/h. 

Fig. 10. Time dependence of corrosion rate of Co8P and Co films, electrolessly plated and sputter-deposited onto NiP substrates, in a droplet of DI water. The results were obtained by a repeated application of the polarization resistance technique with the potential scanned at 1 mV/sec in a potential range 15 mV above and below the corrosion potential [125]. (Reprinted by permission of The Electrochemical Society). 

In conventional electrochemistry in solution, quantitation of analytes can be obtained by using several techniques. Thus, exhaustive electrolysis provides an absolute quantitation of an electroactive component in the sample. Voltammetric measurements (linear potential scan, cyclic, pulse, and square-wave techniques) can be used for determination of analytes in solution via calibration because peak currents (and peak areas) are usually proportional to the analyte concentration under fixed electrochemical conditions. 

The direct electrochemical measurement of such low corrosion rates is difficult and limited in accuracy. However, electrochemical techniques can be used to establish a database against which to validate rates determined by more conventional methods (such as weight change measurements) applied after long exposure times. Blackwood et al. (29) used a combination of anodic polarization scans and open circuit potential measurements to determine the dissolution rates of passive films on titanium in acidic and alkaline solutions. An oxide film was first grown by applying an anodic potential scan to a preset anodic limit (generally 3.0 V), Fig. 24, curve 1. Subsequently, the electrode was switched to open-circuit and a portion of the oxide allowed to chemically dissolve. Then a second anodic... 

Simultaneous application of spectroscopy in voltammetry — Numerous spectroelectrochemical methods employ spectrometers fast enough to acquire complete spectra within seconds or fractions of a second. Acquisition of spectra during a slow electrode potential scan as employed in -> cyclic voltammetry or during single scan voltammetry can thus be related to a single electrode potential (within a range of a few millivolts or even more narrow). Thus interfacial phenomena as detected with the applied spectroelectrochemical technique can be related to the electrode potential directly even in case of unstable intermediates. 

In-Cell Western (Li-COR Cytoblot) Anti-phospho specific antibody labeled with infrared fluor is used to probe fixed cells on MTP second color can be used for normalization binding detected via laser scanning technique Only requires one antibody has potential for multiplexing to control for total substrate expression in cells Multiple wash steps requires cell fixation lower throughput Chen (2005)... 

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