Redox couple surface

The diffusion length of photogenerated charge carriers is one of the important parameters governing the efficiency of a solar cell. In conventional cells, this is an intrinsic property of the semiconductor and its purity [34]. However, in DSSCs, the diffusion length is a function of the rate of reaction (4) and, thus, varies with different redox couples, surface treatments, and so forth. When the oxidation of R [reaction (2)] is chemically irreversible, the diffusion length of electrons is effectively infinite, whereas with kinetically fast, reversible redox couples (see Section VI), it approaches zero with unpassivated interfaces. 

Electrode type Boron Redox couple Surface Surface Surface... 

The active site on the surface of selective propylene ammoxidation catalyst contains three critical functionalities associated with the specific metal components of the catalyst (37—39) an a-H abstraction component such as Sb ", or Te" " an olefin chemisorption and oxygen or nitrogen insertion component such as Mo " or and a redox couple such as Fe " /Fe " or Ce " /Ce" " to enhance transfer of lattice oxygen between the bulk and surface... 

FIGURE 2-3 Concentration distribution of the oxidized and reduced forms of the redox couple at different times during a cyclic voltammetric experiment corresponding to the initial potential (a), to the formal potential of the couple during the forward and reversed scans (b, d), and to the achievement of a zero reactant surface concentration (c). 

The oxidation or reduction of a substrate suffering from sluggish electron transfer kinetics at the electrode surface is mediated by a redox system that can exchange electrons rapidly with the electrode and the substrate. The situation is clear when the half-wave potential of the mediator is equal to or more positive than that of the substrate (for oxidations, and vice versa for reductions). The mediated reaction path is favored over direct electrochemistry of the substrate at the electrode because, by the diffusion/reaction layer of the redox mediator, the electron transfer step takes place in a three-dimensional reaction zone rather than at the surface Mediation can also occur when the half-wave potential of the mediator is on the thermodynamically less favorable side, in cases where the redox equilibrium between mediator and substrate is disturbed by an irreversible follow-up reaction of the latter. The requirement of sufficiently fast electron transfer reactions of the mediator is usually fulfilled by such revemible redox couples PjQ in which bond and solvate... 

Fig. 5.13 Energy level diagram comparing the surface band edge positions of SnS and the energies corresponding to selected redox couples and corrosion reactions involving the semiconductor. (Reproduced from [198])...

Singh P, Singh R, Gale R, Rajeshwar K, DuBow J (1980) Surface charge and specific ion adsorption effects in photoelectrochemical devices. J Appl Phys 51 6286-6291 Bard AJ, Bocarsly AB, Pan ERF, Walton EG, Wrighton MS (1980) The concept of Fermi level pinning at semiconductor/liquid junctions. Consequences for energy conversion efficiency and selection of useful solution redox couples in solar devices. J Am Chem Soc 102 3671-3677... 

A typical result for DPV In Fig. 4a shows the presence of two redox couples with peak potentials of 0.25 V and 0.19 V ( lOmV). Similar results have also been obtained with SWV. The relative Intensities of the two peaks vary from sample to sample but are always present with activated electrodes. The similarities between the potentials found for the surface species and for the oxidation of ascorbic acid suggest that an ec catalytic mechanism may be operative. The surface coverage of the o-qulnone Is estimated to be the order of 10 mol cm . It Is currently not possible to control the surface concentration of the o-qulnone-llke species or the oxygen content of the GCE surface. 

The additivity principle was well obeyed on adding the voltammograms of the two redox couples involved even though the initially reduced platinum surface had become covered by a small number of underpotential-deposited mercury monolayers. With an initially anodized platinum disk the catalytic rates were much smaller, although the decrease was less if the Hg(I) solution had been added to the reaction vessel before the Ce(lV) solution. The reason was partial reduction by Hg(l) of the ox-ide/hydroxide layer, so partly converting the surface to the reduced state on which catalysis was greater. 

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