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Electroactive Promoters

There are many electrode geometries. Particulate electrodes are discussed in Chapter 5, but there is also the single electrode that has [Pg.50]


What is the relationship between changes in catalyst potential and the associated changes in its work function induced by spillover of the electroactive promoter species to or from the solid electrolyte ... [Pg.610]

The combination of electrochemistry and photochemistry is a fonn of dual-activation process. Evidence for a photochemical effect in addition to an electrochemical one is nonnally seen m the fonn of photocurrent, which is extra current that flows in the presence of light [, 89 and 90]. In photoelectrochemistry, light is absorbed into the electrode (typically a semiconductor) and this can induce changes in the electrode s conduction properties, thus altering its electrochemical activity. Alternatively, the light is absorbed in solution by electroactive molecules or their reduced/oxidized products inducing photochemical reactions or modifications of the electrode reaction. In the latter case electrochemical cells (RDE or chaimel-flow cells) are constmcted to allow irradiation of the electrode area with UV/VIS light to excite species involved in electrochemical processes and thus promote fiirther reactions. [Pg.1945]

In amperometry, the current produced by the oxidation or reduction of an electroactive analyte species at an electrode surface is monitored under controlled potential conditions. The magnitude of the current is then related to the quantity of analyte present. However, as both antibody and antigen are not intrinsically electroactive, a suitable label must be introduced to the immunocomplex to promote an electrochemical reaction at the immunosensors. In this respect, enzyme labels including the... [Pg.154]

It is important to note that not all cations promote Prussian blue/Prussian white electroactivity. Except for potassium, only ammonium (NH4+), cesium (Cs+), and rubidium (Rb+) were found able to penetrate the Prussian blue lattice. Other mono-and divalent cations are considered as blocking ones. [Pg.438]

Some monovalent ions promote the electroactivity of metal hexacyanoferrates rather similarly, which affects selectivity of the corresponding sensors. In particular, it... [Pg.439]

The occurrence of an electron-transfer reaction ensures that an electroactive species has a different number of electrons before and after reaction, so different redox states must of necessity display different spectroscopic transitions, and hence will require different energies E for electron promotion. Accordingly, the colours of electroactive species before and after electron transfer will differ. It follows that all materials will change their spectra following a redox change. [Pg.241]

Even in the solutions of highest resistance given in Table 12.1, the ohmic drop can be calculated to be less than 1 mV for a millimolar solution of electroactive species. In a solvent that does not promote ion pairing, the value of p is, to a first approximation, inversely proportional to the supporting electrolyte concentration. Thus, the ohmic drop in steady-state voltammograms can be adjusted by changing either the concentration of the electrolyte or the electroactive species. [Pg.388]

The Aberystwyth group acknowledge support from the SERC (Electroactive Polymers Specially-Promoted Programme) and from the Treaty of Windsor Anglo-Portuguese Exchange Scheme of the British Council. The USM research was sponsored by the Air Force Office of Scientific Research, Air Force Systems Command, USAF, under Grant Number AFOSR 84-0249. [Pg.264]

Mass transport by diffusion can be regarded as the last resort. When movement of the electroactive species is not promoted by the input of external energy, either electrical (migration) or mechanical (convection), diffusion takes over. The driving force in this case is the... [Pg.351]

This applies when catalytic centers are incorporated as dopants to the lattice of the base porous material. In fact, site isolation of electroactive centers immobilized in microporous materials and doping units in inorganic supports appears to promote efficient electrocatalysis for a variety of analytically significant processes. Some remarks can be made ... [Pg.137]


See other pages where Electroactive Promoters is mentioned: [Pg.50]    [Pg.50]    [Pg.2422]    [Pg.1002]    [Pg.324]    [Pg.325]    [Pg.325]    [Pg.330]    [Pg.301]    [Pg.122]    [Pg.363]    [Pg.366]    [Pg.368]    [Pg.60]    [Pg.158]    [Pg.197]    [Pg.560]    [Pg.564]    [Pg.166]    [Pg.189]    [Pg.572]    [Pg.364]    [Pg.369]    [Pg.99]    [Pg.267]    [Pg.316]    [Pg.163]    [Pg.108]    [Pg.148]    [Pg.246]    [Pg.148]    [Pg.450]    [Pg.39]    [Pg.286]    [Pg.209]    [Pg.366]    [Pg.139]    [Pg.139]    [Pg.186]    [Pg.217]    [Pg.166]   


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Electroactive

Electroactivity

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