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Galvanostatic characteristic

Recent studies of the processes of activation and deactivation111 have shown, as seen in Fig. 20, that the time dependences of the potential, upon the application of current steps, resemble those characteristic of porous film formation and that the differences are of a quantitative nature. The initial part, representing a typical galvanostatic charging curve (with the initial jump due to the... [Pg.436]

Figure 3. Galvanostatic charge/discharge characteristics of a capacitor built from KOH activated carbon A-PM (mass of electrodes 12.2 mg/12.8 mg) 1=2 mA. Electrolytic solution ... Figure 3. Galvanostatic charge/discharge characteristics of a capacitor built from KOH activated carbon A-PM (mass of electrodes 12.2 mg/12.8 mg) 1=2 mA. Electrolytic solution ...
Said subjects are being analyzed in this work. Also, the authors have attempted to show that in order to be suitable for lithium-ion applications, a carbon-based active material has to meet a complex number of physicochemical and electrochemical characteristics. A simple check of galvanostatic behavior, which is often used today to conclude about carbon s suitability for lithium-ion battery technology, is rarely enough for making an accurate assessment. [Pg.231]

The capacity and profile of the galvanostatic cycling curves are among the first key characteristics of the active material. [Pg.233]

An EG G PARC 273 Potentiostat/Galvanostat was used in both the electrolysis and the CV experiments, coupled with an HP 7044B X/Y recorder. A Solartron 1255 HF Frequency Response Analyzer and a Solartron 1286 Electrochemical Interface were employed for the a.c. impedance measurements, using frequencies from 0.1 to 65 kHz and a 10 mV a.c. amplitude (effective) at either the open circuit potential (OCP) or at various applied potentials. As the RE can introduce a time delay at high frequencies, observed as a phase shift owing to its resistance and capacitance characteristics, an additional Pt wire electrode was placed in the cell and was connected via a 6.8 pF capacitor to the RE lead [32-34]. [Pg.74]

Fig. 73. Dynamic behavior in S-NDR systems with high conductivity under galvanostatic conditions [22]. (a) Stable stationary domains for two values of the imposed current density, (b) 7/(4 DL plot showing stable and unstable states. The thin lines denote the homogeneous solutions, the thick ones domain solutions. Solid line stable state dashed line unstable state. The arrows indicate the transitions between homogeneous and domain states that would be observed in a galvanodynamic experiment, (c) Chaotically breathing domains that exist in small parameter regions if the characteristic time of the autocatalytic chemical variable is much faster than that of the double layer potential. Fig. 73. Dynamic behavior in S-NDR systems with high conductivity under galvanostatic conditions [22]. (a) Stable stationary domains for two values of the imposed current density, (b) 7/(4 DL plot showing stable and unstable states. The thin lines denote the homogeneous solutions, the thick ones domain solutions. Solid line stable state dashed line unstable state. The arrows indicate the transitions between homogeneous and domain states that would be observed in a galvanodynamic experiment, (c) Chaotically breathing domains that exist in small parameter regions if the characteristic time of the autocatalytic chemical variable is much faster than that of the double layer potential.
Another important parameter in electrochemical promotion studies is the characteristic rate relaxation time, t, needed for the catalytic rate to reach steady state upon imposition of a constant current (galvanostatic transient). As one would expect and as experiment has clearly shown [13,14], t is always of the order of 2FNg/I (Figure 2) ... [Pg.690]

Russian workers have looked at acoustic waves produced during the electrochemical oxidation of antimony [ 147], almost a reverse application of sonoelectrochemistry. Antimony was anodized in aqueous H3B03 solutions galvanostatically (2.2 x 1(T3 A/cm2) and isothermally (292 K). The formation voltage increased to >200 V with time, which is characteristic of the valve metals. Acoustic waves were observed in this electrochemical oxidation with amplitudes that did not differ essentially from the very beginning of the oxidation. The energy of the acoustic wave had only one sharply distinct peak which coincided in time with the appearance of the electrochemical breakdown products. [Pg.247]

A theoretical analysis has been carried out for galvanostatic and potentiostatic pulse regimes [27]. The idea that developed is a bit the same as backflushing with pressure driven-membrane operation such as microfiltration or ultrafiltration. The time dependencies of the extent of the concentration polarization near the membrane surface during the pulse are described theoretically for both pulse regimes and a qualitative discussion of the pause duration is presented. The main characteristic of the non-stationary process is the transition time between the state without polarization and the state with stationary polarization. [Pg.272]


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See also in sourсe #XX -- [ Pg.79 , Pg.82 , Pg.90 ]




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