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Current density, polymers deposited

The same authors also demonstrated the feasibility of synthesizing ozone and hydrogen peroxide simultaneously using pure water and oxygen as the reactants [71]. Commercially available yS lead dioxide and graphite powders were used as the anode and cathode, respectively. While the lead dioxide was deposited directly onto a solid polymer electrolyte (Nafion 117), the graphite powder was deposited onto a carbon fiber paper and pressed against the membrane. At an applied potential of 4.5 V, with a current density of 2 A/cm, a 4.5% current efficiency was obtained for ozone evolution while the current efficiency for peroxide production was 0.8%. [Pg.392]

The deposition rate of plasma polymerization depends on many experimental factors of glow discharge. A large number of attempts have been made to correlate the polymer deposition rate with such operational variables as flow rate, discharge power, current density, and system pressure. Although reasonable agreement is found... [Pg.71]

The necessary porosity for thicker layers was introduced by appropriate current densities [321-323], by co-deposition of composites with carbon black [28, 324] (cf. Fig. 27), by electrodeposition into carbon felt [28], and by fabrication of pellets from chemically synthesized PPy powders with added carbon black [325]. Practical capacities of 90-100 Ah/kg could be achieved in this way even for thicker layers. Self-discharge of PPy was low, as mentioned. However, in lithium cells with solid polymer electrolytes (PEO), high values were reported also [326]. This was attributed to reduction products at the negative electrode to yield a shuttle transport to the positive electrode. The kinetics of the doping/undoping process based on Eq. (59) is normally fast, but complications due to the combined insertion/release of both ions [327-330] or the presence of a large and a small anion [331] may arise. Techniques such as QMB/CV(Quartz Micro Balance/Cyclic Voltammetry) [331] or resistometry [332] have been employed to elucidate the various mechanisms. [Pg.357]

A third category comprises conducting polymers. The film-forming anodic polymerization of monomers, e.g., pyrrole, leads in the majority of cases to porous or even biporous [28] polymer layers, adhering to the substrate. The porosity can be improv at higher current densities, but the overoxidation limit must be considered. Another improvement is possible in terms of the application of graphite felt as a substrate [28, 58, 455]. Last but not least, the co-deposition of dispersed c.b.s in the electrolyte leads to composites with up to 65 wt% c.b. in the polymer layer for... [Pg.370]

These conducting polymers are sometimes termed organic metals, and their formation as thin-film coatings on an electrode involves nucleation phenomena so perhaps by analogy with metal electrodeposition under ultrasound there have been studies to improve the quality of the deposited materials. Polypyrrole readily forms acceptable films under a wide variety of conditions [174], although there are subtle distinctions in behavior as a result of exact preparation procedure [175], Ultrasound from 38 or 500 kHz baths does not appear to appreciably improve polypyrrole film formation, at least from MeCN electrolyte at the normal current density of 1 mAmp... [Pg.254]

Plasma polymerizations were carried out in an apparatus described previously [4]. This apparatus incorporates a vacuum bell jar containing two parallel circular electrodes spaced 3 cm apart, each having a surface area of 40 cm. Polymer films were deposited in a 20 kHz glow discharge on 0.1 mm thick stainless steel tape placed on the lower electrode. Polymer depositions were performed under the following constant conditions current density, j = 1 mA/cm monomer vapour pressure, p = 0.3 Torr and discharge duration, t = 20 s. ... [Pg.237]

A modification of SPE was reported, using a porous membrane made of polyvinylidene fluoride polymer deposited with thin porous Au filin. CO2 was reduced to CO with the faradaic efficiency 75% at the partial current density 20 mA cm as estimated from the difference of the two currents measured under argon and CO2 atmospheres separately. [Pg.179]

An important one is that deposition occurs on the anode, and it is known (5J that some metal is incorporated into the polymer film, presumably because oxidation of the substrate can compete with polymer deposition. Because of this problem of anodic metal dissolution, cathodic deposition of epoxy resins (9-10) was developed. A second disadvantage in using the polyamic acid is that the formulations used do not deposit an insulating film, and thus the film thickness is not self-limiting. Although this fact may allow quite thick films to be deposited, it also means that the film thickness is not uniform as it will depend on distance from the counter-electrode and other current density effects. [Pg.156]

An alternative is to apply a constant current to drive the reaction. This usually results in more even film growth although local variations in current density will produce a heterogeneous polymer. The rate of polymerization is dictated by the current density applied. Again, if the rate is too low, oxidation without deposition may occur. However, if the rate is too high, the potential may stray into the region where overoxidation of the polymer occurs. [Pg.67]

Table 1. Spin-coated CPB thin film (<20 nm) deposition condition and pentacene-based TFT device performance (mobility and on/off ratio) - polymer/crosslinker concentration ratio (mg/ml mg/ml), solvent, film thickness (D, nm), RMS roughness (p, nm), leakage current density at an electric field of 2 MV/cm (J, A/cm2), mobility (ji, cm2/Vs), and Current On/off Ratio (/<, /< ) ... Table 1. Spin-coated CPB thin film (<20 nm) deposition condition and pentacene-based TFT device performance (mobility and on/off ratio) - polymer/crosslinker concentration ratio (mg/ml mg/ml), solvent, film thickness (D, nm), RMS roughness (p, nm), leakage current density at an electric field of 2 MV/cm (J, A/cm2), mobility (ji, cm2/Vs), and Current On/off Ratio (/<, /< ) ...
To improve the limit-of-detection, we replaced the 16 mm vacuum deposited CuPc/Cgg bilayer devices with 1 mm solution-processed polymer devices based on 1 1 blends by weight of poly(3-hexylthiophene) [P3HT] and [6, 6]-phenyl-C61-butyric acid-methylester [PCBM] - a soluble derivative of Ceo- The P3HT PCBM devices fabricated in our laboratory typically have very low short-circuit dark current densities of <10 mA cm , and are consequently a good choice for high sensitivity detection [21]. The... [Pg.120]


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Current density deposits

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