Metal electrode, role

An interesting idea has been to prepare the photosensitive electrode on site having the liquid play the dual role of a medium for anodic film growth on a metal electrode and a potential-determining redox electrolyte in the electrochemical solar cell. Such integration of the preparation process with PEC realization was demonstrated initially by Miller and Heller [86], who showed that photosensitive sulfide layers could be grown on bismuth and cadmium electrodes in solutions of sodium polysulfide and then used in situ as photoanodes driving the... 

Let us consider a cathode electron transfer process at metal electrode. The role of the electron donor is played here by the metal electrode. The specific feature of this donor consists of the fact that its electron energy spectrum is practically continuous... 

Interfacial water molecules play important roles in many physical, chemical and biological processes. A molecular-level understanding of the structural arrangement of water molecules at electrode/electrolyte solution interfaces is one of the most important issues in electrochemistry. The presence of oriented water molecules, induced by interactions between water dipoles and electrode and by the strong electric field within the double layer has been proposed [39-41]. It has also been proposed that water molecules are present at electrode surfaces in the form of clusters [42, 43]. Despite the numerous studies on the structure of water at metal electrode surfaces using various techniques such as surface enhanced Raman spectroscopy [44, 45], surface infrared spectroscopy [46, 47[, surface enhanced infrared spectroscopy [7, 8] and X-ray diffraction [48, 49[, the exact nature of the structure of water at an electrode/solution interface is still not fully understood. 

Polymers have served roles in PEM fuel cell cathodes such as modifiers to macrocycle-based electrodes to improve conductivity and stability,165 composite materials with heteropolyacids,166 and as precursors to pyrolyzed catalysts.38,112,132,133 However, as discussed in the previous section, the activity of nitrogen-containing carbon raises the possibility of non-metal electrodes functioning in a cathode environment. Likewise, researchers have noted ORR activity for various conducting polymers containing nitrogen, and recently studies on their potential use in PEM fuel cell cathodes have been reported. 

While considering trends in further investigations, one has to pay special attention to the effect of electroreflection. So far, this effect has been used to obtain information on the structure of the near-the-surface region of a semiconductor, but the electroreflection method makes it possible, in principle, to study electrode reactions, adsorption, and the properties of thin surface layers. Let us note in this respect an important role of objects with semiconducting properties for electrochemistry and photoelectrochemistry as a whole. Here we mean oxide and other films, polylayers of adsorbed organic substances, and other materials on the surface of metallic electrodes. Anomalies in the electrochemical behavior of such systems are frequently explained by their semiconductor nature. Yet, there is a barrier between electrochemistry and photoelectrochemistry of crystalline semiconductors with electronic conductivity, on the one hand, and electrochemistry of oxide films, which usually are amorphous and have appreciable ionic conductivity, on the other hand. To overcome this barrier is the task of further investigations. 

In this chapter, the application of polarography in the determination of benzodiazepines is emphasized in which this method has played an outstanding role but it can be also useful with some other psychotherapeutics such as fluorine-substituted butyrophenones [240] or those with seven-membered, possibly heterocyclic rings [241] such as in imipramine. In the latter case, anodic oxidation waves are obtained with rotated noble metal electrodes. 

The theoretical treatment of electron transfer at metal electrodes has much in common with that for homogeneous electron transfer described in 12.2.3. The role of one of the reactants is taken by the electrode surface, which provides a rigid two-dimensional environment where reaction occurs. In some respects, electrode reactions represent a particularly simple class of electron-transfer reactions because only one redox center is required to be activated prior to electron transfer, and the proximity of the electrode surface often may yield only a weak, nonspecific influence on the activation energetics of the isolated reactant. As with homogeneous electron transfer, it is useful to consider that simple electrochemical reactions occur in two steps (1) formation from the bulk reactant of a precursor state with the reacting species located at a suitable site within the interphasial region where electron transfer can occur (2) thermal activation of the precursor species leading to electron transfer and subsequent deactivation to form the product successor state. 

The most recent experimental work has involved studies of organic adsorption at the single crystal faces of polarizable solid metal electrodes [57]. These experiments provide details of the role of the metal in organic adsorption. By examining these data within the context of the new molecular descriptions of interfacial adsorption the theory of this important process will be greatly advanced. 

Light energy may be used to reduce the necessary electrical potential in photoelectrochemical reactions. The overpotential is decreased by 700 mV for the photoelectrochemical reduction of CO on p-CdTe, compared to that on indium - the best metal electrode for CO2 reduction. For these semiconductors which involve a high concentration of surface states, the double layer at the semiconductor-electrolyte interface plays an important role in the kinetics of photoelectrochemical reactions. In this paper, we report spectroscopic and impedance aspects of the electrode-electrolyte interface as affected by reactants and radicals involved in CO reduction. 

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