Structural modified electrodes

Measurements of the double-layer capacitance provide valuable insights into adsorption and desorption processes, as well as into the structure of film-modified electrodes (6). 

Some porous ceramic structures of oxides on titanium (CT2O3, RuOj, MnOj, VOJ obtained by baking films of metal complexes like acetylacetonates on titanium surfaces can also be regarded as chemically modified electrodes Applications... 

SETM) give hope that the full structural characterization of modified electrodes will be achieved in the near future. 

Chemical and electrochemical techniques have been applied for the dimensionally controlled fabrication of a wide variety of materials, such as metals, semiconductors, and conductive polymers, within glass, oxide, and polymer matrices (e.g., [135-137]). Topologically complex structures like zeolites have been used also as 3D matrices [138, 139]. Quantum dots/wires of metals and semiconductors can be grown electrochemically in matrices bound on an electrode surface or being modified electrodes themselves. In these processes, the chemical stability of the template in the working environment, its electronic properties, the uniformity and minimal diameter of the pores, and the pore density are critical factors. Typical templates used in electrochemical synthesis are as follows ... 

The indicated formal potential E° n of the corresponding monomer (-1.17V) in solution is very near that of the surface film (-1.13V vs. SSCE). That formal potentials of surface films on chemically modified electrodes are near those of their corresponding dissolved monomers (13,18) is actually a common, and quite useful, observation. In the present case, it demonstrates that the electronic structures of the porphyrin rings embedded in the polymer film are not seriously perturbed from that of the monomer. 

The analytical performance of Prussian blue-modified electrodes in hydrogen peroxide detection were investigated in a flow-injection system equipped with a wall-jet cell. Nano-structured Prussian blue-modified electrodes demonstrate a significantly decreased background, which results in improved signal-to-noise ratio. 

Surfactant has a similar amphoteric structure as lipid, which makes it possible to form a stable membrane the same as a lipid membrane and can be used to embed proteins. A surfactant membrane has many characteristics similar to those of a biomembrane, so that it can retain the bioactivities of proteins well. The process of preparing a sur-factant/protein-modified electrode is simple and viable. There are usually two methods... 

In Situ Surface Extended X-ray Absorption Fine Structure at Chemically Modified Electrodes... 

While the structure of nonredox polymer and polyelectrolytes thin layers has received much attention in the past [116, 117], only recently has a molecular theory able to treat, from a molecular point of view, redox polyelectrolytes adsorbed on electrodes, been presented [118-120]. The formulation of the theory, its scope, advantages and limitations will be discussed in detail in Section 2.5.2, and therefore we will limit ourselves to show here some predictions that are relevant for the understanding of the structure of polyelectrolyte-modified electrodes. The theory was applied to study the particular system depicted in Figure 2.5, which consists of a single layer of PAH-Os adsorbed on a gold surface thiolated with negatively charged mercapto... 

From a survey of the literature in chemically modified electrodes [13], one can identify simple phenomenological models that have been very successful for the analysis of a particular aspect of the experimental data. Such models are, for instance, the Dorman partition model [24, 122], the Laviron [158], Albery [159] and Anson models [127] to account for the nonideal peak width, the Smith and White model for the interfacial potential distribution [129], and so on. Most of these models contain one or more adjustable parameters that give some partial information about the system. For example, the lateral interaction model proposed by Anson [127] provides a value for the lateral interactions between oxidized and reduced sites, but does not explain the origin of the interactions, neither does it predict how they depend on the experimental conditions or the polymer structure. In addition, none of these models provide information on the interfacial structure. 

In general, the electrochemical performance of carbon materials is basically determined by the electronic properties, and given its interfacial character, by the surface structure and surface chemistry (i.e. surface terminal functional groups or adsorption processes) [1,2]. Such features will affect the electrode kinetics, potential limits, background currents and the interaction with molecules in solution [2]. From the point of view of electroanalysis, the remarkable benefits of CNT-modified electrodes have been widely praised, including low detection limits, increased sensitivity, decreased overpotentials and resistance to surface fouling [5, 9, 11, 17]. 

Figure 5.12 Possibilities to deposit metal onto a SAM-modified electrode, (a) intercalation of metal at the SAM/substrate interface, (b) deposition originating at the substrate with subsequent mushroom-like growth, (c) deposition on top of a SAM resulting in a metal-SAM-metal sandwich structure.

Figure 5.17 Illustration of different pathways for growth of a U PD layer on a SAM-modified electrode, (a) Uniform penetration across the whole SAM area, (b) deposition starting at a major defect with subsequent penetration at edge ofUPD island (1), penetration through SAM across the whole U PD area due to the distortion of SAM structure by UPD (2) and growth of UPD island through initial defect only (3).

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