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Electron extract

Electron donor adsorbates, such as atomic H or alkalis or olefins, decrease in general the work function of the substrate. The dipole formed by the adsorbate has its positive end pointing to the vacuum. This facilitates electron extraction from the metal, thus decreases O. [Pg.280]

Here Zg is the number of tt electrons provided by atom is essentially an ionization potential for an electron extracted from in the presence of the part of the framework associated with atom r alone (a somewhat hypothetical quantity), is a framework resonance integral, and is the coulomb interaction between electrons in orbitals < >, and <(>,. The essential parameters, in the semi-empirical form of the theory, are cug, and and from their definition these quantities are expected to be characteristic of atom r or bond r—s, not of the particular molecule in which they occur (for a discussion see McWeeny, 1964). In the SCF calculation, solution of (95) leads to MO s from which charges and bond orders are calculated using (97) these are used in setting up a revised Hamiltonian according to (98) and (99) and this is put back into (95) which is solved again to get new MO s, the process being continued until self-consistency is achieved. It is now clear that prediction of the variation of the self-consistent E with respect to the parameters is a matter of considerable difficulty. [Pg.132]

Fig. 5. 23 Schematic of a scanning ion microscope codeveloped by the University of Chicago Ion Microscopy Group and GMHE/Hughes Research Laboratories, and also the secondary ion and electron extracting part qf the instrument. (Courtesy of R. Levi-Setti.)... Fig. 5. 23 Schematic of a scanning ion microscope codeveloped by the University of Chicago Ion Microscopy Group and GMHE/Hughes Research Laboratories, and also the secondary ion and electron extracting part qf the instrument. (Courtesy of R. Levi-Setti.)...
Alteration of the silver plasmon band spectrum upon electron and hole injection has been rationalized in terms of changes in the density, Ne, and conductivity, o, of the electron gas in the metal particles as described by Eqs. (16)—(18) [506]. Thus, a decrease in Ne by electron extraction from the metallic silver particles increases Xc (Eq. 16) and thereby shifting the absorption maximum (Eq. 15) of the plasmon band to a longer wavelength (Fig. 83). A decrease in Ne also decreases a (Eq. 18), which leads, in turn, to an increase of w (Eq. 17) that is, to an increase in the bandwidth of the plasmon band absorption (Fig. 83). Similarly, the increase in Ne by electron transfer to the silver colloids is paralleled by a decrease in Xc (Eq. 16) and, hence, by a decrease in Xm (Eq. 15), as seen by the shift of the plasmon absorption band to a shorter wavelength (Fig. 83). Electron donation to the silver particles also causes an increase in cr (Eq. 18)... [Pg.104]

This small current is normally quite steady, and may be about 10 nanoamperes. If, however, certain impurities are added to the gas stream, the impurity molecules may capture some of the free electrons before they can be extracted by the electrode. The drop in the number of electrons extracted causes a drop in the electrode current this drop in current signals the presence of the impurity... [Pg.511]

EtMe2PhPb, Benzene hexane Capillary Electron Extraction from l-20pg... [Pg.351]

The amount of electrons extracted from the microplasma, the ionization rate of the sample gas, and the mean free path length depend on the pressure at the different locations of PIMMS-chip. Therefore, exact knowledge and control of pressure and gas flow rates will be necessary for quantitative analysis. Pressure sensors, valves for gas inlets, and vacuum pumps are the components, which have to be read out and controlled, respectively, by electronic and software to install and stabilize appropriate pressure regimes. [Pg.448]

Instability or noise of any of these sources will lead to loss of resolution and/or sensitivity in the mass-spectra. For example, noise on the electron extraction voltage... [Pg.448]

The A 1A2(m,ji ) or Si state of thiophosgene comes about through the occupation of the ji orbital by an electron extracted from the nonbonding n... [Pg.36]

PSI and PSII. PSII contains the site of water cleavage, and utilizes the electrons extracted from water to reduce plastoquinone to plastoquinol. The latter diffuses through the membrane until it is reoxidized by another membrane protein, the cytochrome bf complex, which transfers the electrons to a water-soluble electron carrier (plastocyanin or cytochrome c6). This carrier in turn is oxidized by PSI, which delivers the electrons via ferredoxin to the enzymes that produce NADPH (Figure 11.6) [12],... [Pg.176]

Dlocik et al. [72] have taken a general approach to the generation collection problem which considers voltage dependent rate constants for electron extraction/injection at the TiO substrate interface. The diffusion controlled limit is obtained by making the rate constant for electron extraction sufficiently large. For illumination from the electrolyte side, the ac photocurrent conversion efficiency d>([Pg.271]

The electric fields at the electrodes are different and can adjust toward equalization of the electron and hole currents (although electron extraction by ITO is not prevented), thus increasing the recombination yield. [Pg.629]

The quantum yield tj of electrons extracted by the laser pulse in the UV highly depends on the material of the photocathode used (Table I),... [Pg.129]

ESD induced by electrons extracted at the tip of a scanning tunnelling microscope (STM) has recently applied to the study of the H-Si and Cl-GaAs(l 10) systems by Shen and Avouris [98]. A feature of the STM is the capability to provide an intense electron density (lO A/cm ) of atomic dimensions directly at the surface atoms. Under these conditions, desorption can also proceed with multiple-vibrational excitation. A combination of ESD and STM holds promise as a tool for atomistic DIET, also as a means to asses the influence of electron irradiation at surfaces [99]. In ESDIAD an interesting aspect is the determination of the trajectory of the ion on leaving the surface, which will be discussed later in relation to the TiOa surface. [Pg.616]

The Nernst equation takes into account the thermodynamics of the two redox reactions (fast in the sense of the kinetics of the heterogeneous electron transfer, but here in the absence of associated chemical reactions). The thermodynamic properties of a redox reaction are described by the standard potentials, E°, and the concentrations of the redox species at the electrode surface. At the anode, we have an electron extraction from the electroactive species, and at the cathode the electron is donated to an electroactive species to effect a reduction. These processes may be represented in the general form as ... [Pg.322]

It is of interest to note that each successive S-state transition becomes slower by a factor of 3.5. This trend is understandable on the basis of electrostatic consideration each S-state advance increases the oxidizing equivalent of the S-state by one unit and thus raises the electrical repulsion between it and the positively-charged secondary donor Z. As an S-state oxidation is due to an electron extraction by the oxidized secondary donor Z , it is expected that the rates of formation of the S-states listed above to be the same as those for reduction of Z . This is indeed the case as indicated by the decay of the SIl signals determined by EPR spectroscopy (see Chapter 22). [Pg.363]

Two major effects were proposed as causes for improved electron extraction (a) upon sublimation of the subsequent aluminum layer the liF dissociates, whereby metallic Li atoms may be formed that consequently n-dope the organic semiconductor (fullerene or polymer) under formation of li" and, e.g., AIF3 [86,94,96] or (b) the liF layer could result in an interfacial dipole layer shifting the work function of the electrode [82,90,91]. Both of these viewpoints have been shown to hold merit, as it was demonstrated by photoelectron spectroscopy that for very thin (sub-nanometer) layers of LiF dissociation and consequent n-type doping occurred, whereas for thicker layers (a few nanometers) the formation of a dipole was evidenced [97]. [Pg.14]

This vertical phase segregation led to largely improved device characteristics (EQEs of 10-20%), which were accounted for by an optimized charge transport due to the F8BT being solely in contact with the electron-extracting alumimun electrode [241]. [Pg.50]


See other pages where Electron extract is mentioned: [Pg.361]    [Pg.161]    [Pg.162]    [Pg.257]    [Pg.188]    [Pg.367]    [Pg.263]    [Pg.428]    [Pg.449]    [Pg.156]    [Pg.263]    [Pg.229]    [Pg.232]    [Pg.181]    [Pg.422]    [Pg.423]    [Pg.792]    [Pg.4120]    [Pg.195]    [Pg.545]    [Pg.132]    [Pg.213]    [Pg.25]    [Pg.136]    [Pg.275]    [Pg.302]    [Pg.229]    [Pg.232]    [Pg.163]    [Pg.111]    [Pg.143]    [Pg.152]    [Pg.385]   
See also in sourсe #XX -- [ Pg.236 ]




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Extraction of Electron Transfer Kinetics from Cyclic Voltammetric Signals. Comparison with Other Techniques

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