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Accumulation electron

The plus and minus signs imply that electrons accumulate in the overlap region when the orbitals are combined in phase and out of phase, respectively. The cyclic orbital interaction gives rise to stabilization when the orbitals between a and b, between b and c, and between b and c are combined in phase and when a and b are combined out of phase. These are the orbital phase conditions for the A—>C delocalization in the trienes. When all the phase conditions are simultaneously satisfied, the orbital phase is continuous. [Pg.88]

When a zinc strip is dipped into the solution, the initial rates of these two processes are different. The different rates of reaction lead to a charge imbalance across the metal-solution interface. If the concentration of zinc ions in solution is low enough, the initial rate of oxidation is more rapid than the initial rate of reduction. Under these conditions, excess electrons accumulate in the metal, and excess cationic charges accumulate in the solution. As excess charge builds, however, the rates of reaction change until the rate of reduction is balanced by the rate of oxidation. When this balance is reached, the system is at dynamic equilibrium. Oxidation and reduction continue, but the net rate of exchange is zero Zn (.S ) Zn (aq) + 2 e (me t a i)... [Pg.1379]

At the interface of the nitride (Ef, = 5.3 eV) and the a-Si H the conduction and valence band line up. This results in band offsets. These offsets have been determined experimentally the conduction band offset is 2.2 eV, and the valence band offset 1.2 eV [620]. At the interface a small electron accumulation layer is present under zero gate voltage, due to the presence of interface states. As a result, band bending occurs. The voltage at which the bands are flat (the flat-band voltage Vfb) is slightly negative. [Pg.178]

The rate of electron accumulation at ionized traps in the depletion zone of the Schottky barrier in the Au/ZnO contact is in proportion to the concentration of unoccupied traps, frequency of metal parti-cle/metastable atom interaction events, and to the probability of electron capture per a trap in a single event of interaction between metastable atoms and metal particle. [Pg.336]

ToF-MS does not scan, the ions are pulsed into the analyser and the electronics accumulate 40 000 spectra per second, which are averaged and saved up to 500 times per second. GC-oaToFMS instruments are... [Pg.459]

The first order term in A/p comes from the difference of the potential energy and the higher order terms should be included when AIP/UP is not small enough. The phases, which the freed electrons accumulate during their different quantum paths, are transferred to the harmonics through the coherent process of HHG and lead to the interferences (Fig. 4.1). [Pg.68]

The extreme strength of the covalent bond derives from the way electrons accumulate between the two atoms. The space occupied by the electrons as they accumulate is not random rather, the two electrons occupy a molecular orbital that is orientated spatially in such a way that the highest probability of finding the electronic charges is directly between the two atomic nuclei. [Pg.64]

In a pericyclic reaction, the electron density is spread among the bonds involved in the rearrangement (the reason for aromatic TSs). On the other hand, pseudopericyclic reactions are characterized by electron accumulations and depletions on different atoms. Hence, the electron distributions in the TSs are not uniform for the bonds involved in the rearrangement. Recently some of us [121,122] showed that since the electron localization function (ELF), which measures the excess of kinetic energy density due to the Pauli repulsion, accounts for the electron distribution, we could expect connected (delocalized) pictures of bonds in pericyclic reactions, while pseudopericyclic reactions would give rise to disconnected (localized) pictures. Thus, ELF proves to be a valuable tool to differentiate between both reaction mechanisms. [Pg.431]

When a difference of potential AE is applied to the two plates, an excess q of electrons accumulates on one of them (which is equal to the... [Pg.43]

The rate of flow of electrons from such a charged particle depends on the availability of an accessible site for this transfer. Although it is known that lattice defects provide such sites and that conduction band electrons can trickle down through solid dislocation levels reduction sites for electron accumulation are usually provided by metallization of the semiconductor particle. This can be achieved through photo-platinization or by a number of vapor transfer techniques and the principles relevant to hydrogen evolution on such platinized surfaces have been delineated by Heller The existence of such sites will thus control whether single or multiple electron transfer events can actually take place under steady state illumination. [Pg.81]

Once the dye molecules are stoichiometrically reduced, the photogenerated electrons accumulate within the colloidal particles. This is evident from the broad absorption band in the near-IR region of the spectrum d (Fig. 2A) which was recorded 20 min after photolysis. [Pg.313]

Figure 12 Principle of charge separation in semiconductor heterostructures (a) capped (or Core-Shell) geometry and (b) coupled geometry. Electrons accumulate at the conduction band (CB) of Sn02 while holes accumulate at the valence band (VB) of Ti02. Figure 12 Principle of charge separation in semiconductor heterostructures (a) capped (or Core-Shell) geometry and (b) coupled geometry. Electrons accumulate at the conduction band (CB) of Sn02 while holes accumulate at the valence band (VB) of Ti02.
Wang, C. M. Heller, A. Gerischer, H. Palladium catalysis of 02 reduction by electrons accumulated on Ti02 particles during photoassisted oxidation of organic compounds, J. Am Chem Soc. 1992, 114, 5230. [Pg.340]

Boschloo G., Fitzmaurice M. (1999) Electron Accumulation in Nanostructured Ti02 (Anatase) Electrodes, J. Phys. Chem. B. 103(37), 7860-7868. [Pg.598]

Electrons accumulate in the space-charge layer by injection, giving rise to an accumulation layer. [Pg.63]

Fig. 1. (a and b) Specimen geometries used in the field-effect experiments. S, D, and G represent the source, drain, and gate electrodes Q is a thin quartz dielectric, (c) Band diagram showing the formation of an electron accumulation layer near the surface between x = 0 and x — X. The electric field e from the positive gate electrode induces a charge —qin the a-Si H. The tail-state distribution TS between Ec and EA is likely to limit the band bending at the surface. [Pg.91]

Typical ON-OFF drain current ratio in the best reported FETs can be as high as 10s or better. The remarkable rise in 7d is caused by an electron accumulation layer formed at the a-Si H insulator interface, which creates an efficient path between the source and drain electrodes. [Pg.231]

Fig. 16.20 Electron accumulation in Ag/Ti02 core-shell particles [Reprinted with permission from Hirakawa and Kamat (2004). Copyright (2004) American Chemical Society]... Fig. 16.20 Electron accumulation in Ag/Ti02 core-shell particles [Reprinted with permission from Hirakawa and Kamat (2004). Copyright (2004) American Chemical Society]...
Figure SI. Radial charge density plot for the resonant FD amplitude in e-Ca scattering. The number of radial nodes for the resonant FD amplitude identifies it as a Sp-iype orbital with a predominantly dp-type character. The role of optimal theta (9opt = 0.S9 radians) in accumulation of electron density near the nucleus is evident. The electron density for the temporarily captured electron accumulates at rmat = IS a.u. indicating that the impinging electron stays far away even from the outermost valence electrons of the target. Figure SI. Radial charge density plot for the resonant FD amplitude in e-Ca scattering. The number of radial nodes for the resonant FD amplitude identifies it as a Sp-iype orbital with a predominantly dp-type character. The role of optimal theta (9opt = 0.S9 radians) in accumulation of electron density near the nucleus is evident. The electron density for the temporarily captured electron accumulates at rmat = IS a.u. indicating that the impinging electron stays far away even from the outermost valence electrons of the target.
Electronic accumulation represents probe interaction within electric fields. Small electrodes are arranged in an array and are addressed by electric circuits. Thus, charged capture probes are mutually attached or appealed in the discharged flow-through cell [50]. The capture probe concentration is enhanced on positive or negative electrodes. Nanogen uses Streptavidin coated gold electrodes to couple biotinylated capture probes after electronic accumulation (Fig. 18). [Pg.21]

Fig. 18 Scheme showing electronic accumulation of negatively charged biotinylated capture probes coupling on positive Streptavidin coated electrodes. With negative switched phase electrodes the negatively charged will be repealed... [Pg.22]


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