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Conduction hand

The cathodic current of electron transfer is proportional to the concentration of interfadal electrons, n and the anodic current of hole transfer is proportional to the concentration of interfacial holes, p., in semiconductor electrodes as described in Sec. 8.3. Since the concentration of interfacial electrons or holes depends on the quasi-Fermi level of interfacial electrons or holes in the electrode as shown in Eqn. 10-3 or 10—4 (n, = n + dra and p, =p + 4P ), the transfer current of cathodic electrons or anodic holes under the condition of photoexdtation depends on the quasi-Fermi level of interfadal electrons, nCp, or the quasi-Fermi level of interfadal holes, pEp It also follows from Sec. 8.3 that the anodic current of electron transfer (the ipjection of electrons into the conduction hand) or the cathodic current of hole transfer (the ipjection of holes into the valence band) does not depend on the... [Pg.328]

Fig. 15 Simplified schematic representation of the electronic energy levels in a single-layer PLED. CB and VB are the conduction hand and valence hand, respectively, of the semiconducting polymer, which correspond to the ionization potential (IP) and electron affinity (EA) relative to vacuum level (EV). The work functions for anode (and cathode ( Fig. 15 Simplified schematic representation of the electronic energy levels in a single-layer PLED. CB and VB are the conduction hand and valence hand, respectively, of the semiconducting polymer, which correspond to the ionization potential (IP) and electron affinity (EA) relative to vacuum level (EV). The work functions for anode (and cathode (<Pc) and the band gap (EG) are also indicated...
The remaining unfilled orbitals form higher-energy bands, called the conduction hand. Keep in mind that even though the d and / orbitals may not be filled with electrons, they still exist for many of the heavier elements, so they must be included in the molecular orbital diagram. We will see later in Chapter 6 that the conduction band plays a very important role in the electrical, thermal, and optical properties of metals. [Pg.28]

According to the electron-transfer mechanism of spectral sensitization, the transfer of an electron from the excited sensitizer molecule to the silver halide and the injection of pholoeleclrous into die conduction band are the primary processes. Thus, the lowest vacant level of the sensitizer dye is situated higher than the bottom of the conduction hand. The regeneration of the sensitizer is possible by reactions of the positive hole to form radical dications. If the highest filled level of the dye is situated below the top of the valence band, desensitizatinn occurs because of hole production. [Pg.1351]

In a light-emitting diode (LED), which is used in displays on electronic equipment, watches, and clocks, a voltage is imposed across an n-p semiconductor junction. The electrons on the n side combine with the holes on the p side and emit light at the frequency of the hand gap. This process can also be described as the emission of light as electrons fall from levels in the conduction hand to empty levels in the valence band. It is the reverse of the production of electric current by illumination of a semiconductor. [Pg.927]

Xi02 (b) Excitation scheme for two-step photon absorption in the PhS/Ti02 heterostructure, involving excitation from the Xi02 valence hand to Xi02 surface states, to PbS quantum-dot states, to PbS excited states and finally to Xi02 conduction-hand states. [Pg.441]

Figure 12. Effect of surface complexation on absorption spectra of TiOz transparent sols (0.5 g/L) and on the kinetics of electron transfer from the conduction hand of TiOz to methyl viologen. Part a Addition of salicylic acid and catechol (2 X 10 M) produces a red shift of the absorption onset to 500 and 600 nm, respectively. Part b Oscillograms showing the temporal behavior of the 600-nm absorbance after laser excitation of water methanol (90 10, v v) degassed solutions containing colloidal TiOz (0.5 g/L), PVA (0.5 g/L), and 10 M MV2+ (bare Ti02 particles) at pH 3.6. Part c Same solution as in Figure 12b, but with 10 M isophthalic acid (1) and 10 3 M salicylic acid (2) added, respectively. (Reproduced from reference 47. Copyright 1991 American Chemical Society.)... Figure 12. Effect of surface complexation on absorption spectra of TiOz transparent sols (0.5 g/L) and on the kinetics of electron transfer from the conduction hand of TiOz to methyl viologen. Part a Addition of salicylic acid and catechol (2 X 10 M) produces a red shift of the absorption onset to 500 and 600 nm, respectively. Part b Oscillograms showing the temporal behavior of the 600-nm absorbance after laser excitation of water methanol (90 10, v v) degassed solutions containing colloidal TiOz (0.5 g/L), PVA (0.5 g/L), and 10 M MV2+ (bare Ti02 particles) at pH 3.6. Part c Same solution as in Figure 12b, but with 10 M isophthalic acid (1) and 10 3 M salicylic acid (2) added, respectively. (Reproduced from reference 47. Copyright 1991 American Chemical Society.)...
Insulator - A material in which the highest occupied energy hand (valence hand) is completely filled with electrons, while the next higher hand (conduction hand) is empty. Solids with an energy gap of 5 eV or more are generally considered as insulators at room temperature. Their conductivity is less than S/m and increases with temperature. [Pg.101]

The stress optical law is maintained during relaxation of a deformed rubber (Figure 6.17) (Balasubramanian et al., 2005) moreover, the same proportionality to An is maintained for the normal components of the stress. And since orientation of rubber also affects heat conduction (Hands, 1980), there is a corresponding proportionality, known as the stress-thermal rule, between sttess and the anisotropy of the thermal conductivity (Venerus et al., 1999) ... [Pg.309]

For clarification of the type of junctions formed at the semiconductor-electrolyte, let us take an example of n-type semiconductor. In addition to possessing free electrons (referred to as the majority carrier), n-type semiconductor also possesses holes (referred to as the minority carrier). The concentration of holes is temperature-dependent and is equivalent to the intrinsic concentration of the carrier (which is related to the concentration of Frankel defects). It can be shown mathematically that the Fermi level of minority carrier hes at almost half the band gap position. On the other hand, the concentration of majority carriers as well as the Fermi level depends on doping concentration. Thus, the Fermi level of the majority carrier can he anywhere between the conduction hand edge and the intrinsic Fermi level that is situated at i g. [Pg.292]

Photocatalytic removal of metals is an important apphcation in its own right. There are three pathways for metal removal, two direct and one indirect. Direct reduction of metal ions hy conduction hand electrons is the simplest way. However, the redox potential of the metallic couple (M +/M ) should he more positive than the conduction band edge (Fig. 14). Experimental results have indicated that... [Pg.552]

In metals, which, of course, are inherently electrically conductive without doping, the valence and conduction hands form a single, overlapping hand. This allows for easy electron mobility through the metal, hence the metallic conductivity. In doped conducting polymers, the conductivity is generally less than, and often considerably less than, that of a metal. There are a few isolated examples of conducting polymers where the conductivity approaches that of a metal like copper. [Pg.440]

In Fig. 4.13, the situation for CaFa is presented however, the presented scheme is qualitatively very similar in other crystals. Especially, it should be emphasized that the lowest state of the 4f 5d electronic configuration for all lanthanides is located near the conduction hand, and its energy with respect to the conduction band is approximately the same for all ions. Thus, different energies of the 4f 5d 4f transitions actually result from different locations of the ground... [Pg.102]

Conduction hand A partially filled band or a band of vacant energy levels just higher in energy than a filled band a band... [Pg.494]

According to the hand theory for elements, the valence electrons are found in a valence hand. If this is only partly filled with electrons, there are occupied and unoccupied levels (with small energy differences) within the valence band. A small electrical po-tenhal difference applied across the crystal excites electrons from the highest (regarding energy) filled levels to unfilled levels immediately above. The unfilled valence band is also a conduction hand, according to Figure 40.11a. This explains the ability of metals to conduct electricity. [Pg.914]

The results showed that the decreased luminescence lifetime ofRu(bpy)3 in Si-Ti oxide xerogels can he mainly attributed to electron transfer from the excited state of Ru(bpy)3+ to the conduction hand of the titania. [Pg.476]

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Lattice parameters of ZnO have been investigated over many decades [22-30]. The lattice parameters of a semiconductor usually depend on the following factors (i) free electron concentration acting via deformation potential of a conduction hand minimum occupied by these electrons, (u) concentration of foreign atoms and defects and their difference of ionic radii with respect to the substituted matrix ion, (iii) external strains (e.g., those induced by substrate), and (iv) temperature. The lattice parameters of any crystalline material are commonly and most accurately measured by high-resolution X-ray diffraction (HRXRD) using the Bond method [31] for a set of symmetrical and asymmetrical reflections. Table 1.2 tabulates measured and calculated lattice parameters, cja ratio, and u parameter reported by several groups for ZnO crystallized in wurtzite, zinc blende, and rocksalt structures for comparison. [Pg.12]

Structureless GL band in ZnO was attributed also to Vzn acceptor [86,118-120], a complex defect involving Zn [121], Oz [122], and Vq [105,106,123-126]. Different authors suggested different types of electron transitions to explain the GL band, for example, from the Vo donor level located near the conduction hand to the valence band (D-h-type recombination) [105], from Vo or another donor level to deep Vzn acceptor level (DAP type) [119,120], from conduction hand to the Vz acceptor (e-A type) [86], and between two states of Vo (intracenter transition) [125]. However, as indicated earlier. Van de Walk [87, 88] predicted that V in ZnO has only the level (2+ /O) at about 2.2 eV above the valence hand. Note also that the D-h-type recomhi-nation is highly improbable in an n-type semiconductor [127]. Moreover, the DAP-type recombination observed in Ref. [120] may not be the same PL hand as others detected because its maximum is at 2.3 eV (shifting to 2.04eV after time delay), which is, in the yellow range. [Pg.187]

In this method, the intermediate states for the first virtual transition in the fourth-order perturbation matrix may correspond to one ion with N electrons and another with N + 1 electrons and one hole in the p-like valence band. The hole may be considered as being created by a valence band electron transferred to the ionic d-shell, as in the case of superexchange. In addition, one ion with N electrons and another with N 1 electrons, and one electron in the conduction hand may also describe the first intermediate state. The electron in question in the conduction band is the one that is transferred from the d-sheD of the ion to the conduction band. The intermediate state after the second transition consists of two ions with N electrons, a hole in the valence band, and an electron in the conduction band. Or it may consist of one ion with N + 1 and the other with N 1 electrons and no holes in the valence band and no electrons in the conduction band. This can pave the way for a ferromagnetic d-d... [Pg.306]


See other pages where Conduction hand is mentioned: [Pg.52]    [Pg.226]    [Pg.409]    [Pg.448]    [Pg.137]    [Pg.38]    [Pg.47]    [Pg.439]    [Pg.440]    [Pg.81]    [Pg.117]    [Pg.157]    [Pg.41]    [Pg.268]    [Pg.290]    [Pg.311]    [Pg.44]    [Pg.501]    [Pg.472]    [Pg.34]    [Pg.168]    [Pg.31]    [Pg.319]    [Pg.57]   
See also in sourсe #XX -- [ Pg.159 , Pg.160 , Pg.172 ]

See also in sourсe #XX -- [ Pg.159 , Pg.160 , Pg.172 ]




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