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Charge transfer indicator variables

Fig. 1.20 Cell consisting of two reversible Ag /Ag electrodes (Ag in AgN03 solution). The rate and direction of charge transfer is indicated by the length and arrow-head as follows gain of electrons by Ag -he- Ag—> loss of electrons by Ag - Ag + e- —. (o) Both electrodes at equilibrium and (f>) electrodes polarised by an external source of e.m.f. the position of the electrodes in the vertical direction indicates the potential change. (K, high-impedance voltmeter A, ammeter R, variable resistance)... Fig. 1.20 Cell consisting of two reversible Ag /Ag electrodes (Ag in AgN03 solution). The rate and direction of charge transfer is indicated by the length and arrow-head as follows gain of electrons by Ag -he- Ag—> loss of electrons by Ag - Ag + e- —. (o) Both electrodes at equilibrium and (f>) electrodes polarised by an external source of e.m.f. the position of the electrodes in the vertical direction indicates the potential change. (K, high-impedance voltmeter A, ammeter R, variable resistance)...
Films have been deposited using selenourea and an ammonia-complexed solution at 65°C [96]. Zincblende CdSe was obtained with an optical spectrum corresponding to a bandgap of 1.84 eV (the bulk room-temperature bandgap of zincblende CdSe is ca. 1.8 eV). Analysis of electrical conductivity measurements indicated charge transfer occurred via a variable hopping mechanism through fairly deep states (a level 0.29 eV below the conduction band was found from these measurements). [Pg.176]

Although the kinetic variable in electrode reactions in the current density, extensive use of the overpotential concept has been made in the electrochemical literature to indicate the departure from equilibrium [7]. Depending on the particular rate-determining process, in the overall electrode kinetics ohmic, charge transfer, reaction, concentration or mass transport, and crystallization overpotentials are described in the literature. Vetter [7] distinguished the concept of overpotential from that of polarization in the case of mixed potentials when the zero current condition does not correspond to an equilibrium potential as will be discussed in Sect. 8. [Pg.7]

Surface condition (3.9) indicates that the surface concentrations of species O and R, Cq and cj(, are not only functions of variable, v[> (i O, R), as in the case of Nemstian charge transfer processes, but also time dependent, since their corresponding derivatives at s = 0 are too. [Pg.136]

Figure 34. 7K absorption and 5K variable-field (0-6.57) MCD spectra of 1.7% Co2+ ZnO nanocrystals. The inset shows the S = saturation magnetization of the LF(o) and BG(a) MCD intensities. Ligand-field (LF), charge-transfer (CT), and band gap (BG) transitions are indicated. [Adapted from (52).]... [Pg.107]

These interactions can be roughly parameterized by the indicator variables and takes the value 1 when X is a charge transfer acceptor and 0 when it is not, while takes... [Pg.423]

Noteworthy, Cq and Cr not only depend on the distance from the electrode, x, which is the source of the perturbation possibly inducing a charge transfer, but also on time, t, indicating the time elapsed from the start of the electrode polarization. Co and Cr will be explicitly considered as functions of both x and f variables from here onwards. [Pg.251]


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