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Charge layers

A quantitative treatment for the depletive adsorption of iogenic species on semiconductors is that known as the boundary layer theory [84,184], in which it is assumed that, as a result of adsorption, a charged layer is formed. Doublelayer theory is applied, and it turns out that the change in surface potential due to adsorption of such a species is proportional to the square of the amount adsorbed. The important point is that very little adsorption, e.g., a 0 of about 0.003, can produce a volt or more potential change. See Ref. 185 for a review. [Pg.718]

As we have discussed earlier in the context of surfaces and interfaces, the breaking of the inversion synnnetry strongly alters the SFIG from a centrosynnnetric medium. Surfaces and interfaces are not the only means of breaking the inversion synnnetry of a centrosynnnetric material. Another important perturbation is diat induced by (static) electric fields. Such electric fields may be applied externally or may arise internally from a depletion layer at the interface of a semiconductor or from a double-charge layer at the interface of a liquid. [Pg.1279]

Figure Bl.28.9. Energetic sitiration for an n-type semiconductor (a) before and (b) after contact with an electrolyte solution. The electrochemical potentials of the two systems reach equilibrium by electron exchange at the interface. Transfer of electrons from the semiconductor to the electrolyte leads to a positive space charge layer, W. is the potential drop in the space-charge layer. Figure Bl.28.9. Energetic sitiration for an n-type semiconductor (a) before and (b) after contact with an electrolyte solution. The electrochemical potentials of the two systems reach equilibrium by electron exchange at the interface. Transfer of electrons from the semiconductor to the electrolyte leads to a positive space charge layer, W. is the potential drop in the space-charge layer.
The interface between a positively or negatively charged electrode and the negatively or positively charged layer of solution in contact with the electrode. [Pg.513]

The potential difference across the mobile part of the diffuse-charge layer is frequently called the zeta potential, = E(0) — E(oo). Its value depends on the composition of the electrolytic solution as well as on the nature of the particle-hquid interface. [Pg.2006]

For many particles, the diffuse-charge layer can be characterized adequately by the value of the zeta potential. For a spherical particle of radius / o which is large compared with the thickness of the diffuse-charge layer, an electric field uniform at a distance from the particle will produce a tangential electric field which varies with position on the particle. Laplace s equation [Eq. (22-22)] governs the distribution... [Pg.2006]

PLATE 5. Propagating brush discharge (PBD) on charged layer initiated by grounded electrode. [Pg.40]

The layer thickness must be less than about 8 mm or air breakdown will occur above the charged layer before the critical surface charge density of 2.5 x 10-" C/m can be attained. [Pg.41]

The breakdown strength of the charged layer must be adequate to attain the critical charge density, implying a certain minimum layer thickness as shown schematically in Figure 2-6.5. [Pg.41]

Although the observations for PPV photodiodes of different groups are quite similar, there are still discussions on the nature of the polymer-metal contacts and especially on the formation of space charge layers on the Al interface. According to Nguyen et al. [70, 711 band bending in melal/PPV interfaces is either caused by surface states or by chemical reactions between the polymer and the metal and... [Pg.590]

Dispersing a dielectric substance such as A1203 in Lil [34] enhances the ionic conductivity of Lil about two orders of magnitude. The smaller the particle size of the dielectrics, the larger is the effect. This phenomenon is explained on the basis that the space-charge layer consists of or Li, generated at the interface between the ionic conductor (Lil) and the dielectric material (A1203) [35],... [Pg.542]

Equations 5.37, 5.38 and 5.39 for solid velocity and pressure drop ate applicable only in the absence of electrostatic charging of the particles. Many materials, including sand, become charged during transport and cause the deposition of a charged layer on the surface of the pipe. The charge remains on the earthed pipeline for long periods but can... [Pg.221]

Before constructing an electrode for microwave electrochemical studies, the question of microwave penetration in relation to the geometry of the sample has to be evaluated carefully. Typically only moderately doped semiconductors can be well investigated by microwave electrochemical techniques. On the other hand, if the microwaves are interacting with thin layers of materials or liquids also highly doped or even metallic films can be used, provided an appropriate geometry is selected to allow interaction of the microwaves with a thin oxide-, Helmholtz-, or space-charge layer of the materials. [Pg.443]

Figure 4a. Electrochemical cells for microwave conductivity measurements. Cell above microwave conduit (1) electrochemical cell (plastic tube, placed on working electrode material), (2) counter-electrode, (3) reference electrode, (4) electrolyte, (5) space charge layer, (6) diffusion layer, (7) contact to working electrode, (8) waveguide. Figure 4a. Electrochemical cells for microwave conductivity measurements. Cell above microwave conduit (1) electrochemical cell (plastic tube, placed on working electrode material), (2) counter-electrode, (3) reference electrode, (4) electrolyte, (5) space charge layer, (6) diffusion layer, (7) contact to working electrode, (8) waveguide.
Another technique consists of MC measurements during potential modulation. In this case the MC change is measured synchronously with the potential change at an electrode/electrolyte interface and recorded. To a first approximation this information is equivalent to a first derivative of the just-explained MC-potential curve. However, the signals obtained will depend on the frequency of modulation, since it will influence the charge carrier profiles in the space charge layer of the semiconductor. [Pg.455]

Relation (18) for the potential-dependent PMC signal is a reasonably good approximation only for the depletion region, where the space charge layer is controlled by the presence of fixed electron donors (Afo). It would become even more complicated if bimolecular or even more complicated kinetic reaction steps were considered. [Pg.463]

The Gartner model simulates charge collection by a potential-dependent space charge layer and considers diffusion into the space charge layer of charge carriers generated deep inside the semiconductor. The well-known Gartner formula for the photocurrent /ph is... [Pg.467]

The decrease of the PMC signal toward increasing depletion therefore reflects the increasing dynamics of minority carriers passing the space charge layer. No classical electrochemical technique has up to now permitted observation of this phenomenon with such clarity. [Pg.483]

Figure 28. Semiconductor interfaces with increasing electric fields in the space charge layer (from top to bottom) compared with tubes of different diameters through which an equivalent amount of water is pressed per unit time (equivalent to limiting current). Figure 28. Semiconductor interfaces with increasing electric fields in the space charge layer (from top to bottom) compared with tubes of different diameters through which an equivalent amount of water is pressed per unit time (equivalent to limiting current).
Interesting results have also been obtained with light-induced oscillations of silicon in contact with ammonium fluoride solutions. The quantum efficiency was found to oscillate complementarity with the PMC signal. The calculated surface recombination rate also oscillated comple-mentarily with the charge transfer rate.27,28 The explanation was a periodically oscillating silicon oxide surface layer. Because of a periodically changing space charge layer, the situation turned out to be nevertheless relatively complicated. [Pg.487]


See other pages where Charge layers is mentioned: [Pg.1946]    [Pg.771]    [Pg.425]    [Pg.495]    [Pg.361]    [Pg.178]    [Pg.2007]    [Pg.27]    [Pg.28]    [Pg.28]    [Pg.30]    [Pg.124]    [Pg.204]    [Pg.352]    [Pg.1168]    [Pg.216]    [Pg.562]    [Pg.459]    [Pg.461]    [Pg.462]    [Pg.462]    [Pg.467]    [Pg.469]    [Pg.472]    [Pg.475]    [Pg.477]    [Pg.481]    [Pg.483]    [Pg.483]    [Pg.483]    [Pg.495]   
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See also in sourсe #XX -- [ Pg.77 ]

See also in sourсe #XX -- [ Pg.398 , Pg.399 , Pg.400 ]

See also in sourсe #XX -- [ Pg.383 , Pg.384 , Pg.429 , Pg.433 ]




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A Charged Surface and Its Double Layer

Adsorbed layer charged surfactants

Also Double layer interaction constant surface charge

Capacitance space charge layer

Catalyst layer charge-transfer resistivity

Celadonite layer charge

Charge Preservation in Negative Electrodes by a PbO Layer

Charge balances, triple-layer model

Charge balances, triple-layer model surface complexes

Charge density wave layered materials

Charge density: diffuse layer

Charge density: diffuse layer metal

Charge density: diffuse layer solution

Charge generation layer

Charge of the double layer

Charge transfer layers

Charge transport layer

Charge transporting layer

Charge-potential relationships electric double layer

Charged Interfaces, Double Layers, and Debye Lengths

Charging of double layers

Charging the Double Layer

Charging voltage, double-layer capacitance

Charging voltage, double-layer capacitance characteristics

Chlorite layer charge

Chronopotentiometry double layer charging

Crystal Structure and Layer Charge of Montmorillonite

Current double-layer charging

Cyclic voltammetry double layer charging effects

Differential electric capacity of space charge layers

Diffuse charge layer

Diffuse double layer charge

Diffuse double layer charge distribution

Double electric charge layer

Double electrical layer diffuse charge density

Double layer capacitance Charging

Double layer charge distribution

Double layer charge transfer

Double layer charge—transfer reaction

Double layer charging cyclic voltammetry

Double layer charging effects

Double layer charging potential-step chronoamperometry

Double layer space-charge regions

Double layer surface charge

Double layer, capacitance/capacitor charging

Double layer, charge

Double-electric layer charge density

Double-layer charging

Double-layer charging time constant

Double-layer charging/discharging

Dual charge generation layer

Dual charge transport layer

Electrical double layer charge density

Electrical double layer charge distribution

Electrical double layer, surface charge

Electrochemical double layer charge neutrality

Electron tunneling through the space charge layer

Electronic properties, passive layers charge transfer

Field space charge layer

Fuel cell double layer charging

Glauconite layer charge

Gouy-Chapman charge layer

Gouy-Chapmen space charge layer

Helmholtz charge layer

INDEX layer charge

Layer charge density

Layer charging

Layer-charge distribution

Layered Heterometallic Vanadates Charge Density Matching

Linear double-layer-charging currents

Montmorillonite layer charge

Multilayer Devices The Incorporation of Charge-Transporting Layers

Neglect of double-layer charging chronopotentiometry

Nonuniformly Charged Surface Layer Isoelectric Point

Permselectivity charged layer

Phyllosilicates layer charge

Potential across the space charge layer

Potential distribution across a surface charge layer

Quantized double layer charging

Range of layer charges

Recombination in the space charge layer

Replacement of cations to form charged layers

Schottky layers, charge carrier density

Schottky surface charge layer

Semiconductor electrode space-charge layer

Silicate clays layer charge

Space Charge Layer and Band Banding

Space Charge Layers in Semiconducting Ceramic Materials

Space charge boundary layer

Space charge layer

Space charge layer Subject

Space charge layer band bending

Space charge layer definition

Space charge layer doping

Space charge layer formation

Space charge layer formation interface

Space charge layer metal deposit

Space charge layer potential distribution

Space charge layer potential drop

Space charge layer semiconductor

Space charge layer thickness

Space charge layer width

Space charge layers, schematic diagram

Space-charge layers chemisorption

Space-charge layers oxide layer

Surface Charge and Debye Layer Capacitance

Surface Charge and the Electric Double Layer

Surface Charges and Electrical Double Layer Background

Surface charge density diffuse double layer

Surface charge layer

The Charge Double Layer

The Space Charge Layer

The electrolyte double layer surface tension, charge density, and capacity

The space charge layer within semiconductor particles

Theory of Space-Charge Layers

Thick Surface Charge Layer and Donnan Potential

Thickness of the space charge layer

Vermiculite layer charge

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