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Conducting excitations

Conductances" Excit TCation Excit iKtot Inhib Tks Excit T IH Inhib T KV3 Excit i Iko, Reduced cell firing by inhibition of high-voltage-activated Ca channels Unknown but likely to be similar to H3... [Pg.255]

Fig. 11.3. Raman spectrum of boron-dopedpotycrystaUine diamond showing metallic conductivity. Excitation line ro aser was 514.51... Fig. 11.3. Raman spectrum of boron-dopedpotycrystaUine diamond showing metallic conductivity. Excitation line ro aser was 514.51...
Structure defects decrease conductivity of the studied material, and then the intensity of the induced magnetic field is small and the signal received by the probe Hp is big (Fig.2). Low conductivity of austenite is a defects of the structure in case of residual austenite in the martensite structure, which with regard to the magnesite structure is as 1 5. Eddy currents produced in the studied area are subject to excitation in effect of small conductivity of austenite grains in the structure of the studied material. [Pg.20]

In order to realise such a high dynamic range, either a local compensation coil at the location of the SQUID [9] or a gradiometric excitation coil like the double-D coil have to be used. In case of the electronic compensation, the excitation field and the response of the conducting sample is compensated by a phase shifted current in an additional coil situated close to the SQUID-sensor. Due to the small size of this compensation coil (in our case, the diameter of the coil is about 1 mm), the test object is not affected by it. [Pg.259]

The accuracy of the calculated solution is highly depending of realistic values for conductivity and permeability of the tube material. While the conductivity can be found in the literature for most materials, the right permeability is harder to determine. In the RFEC technique the exciter current and thus the exciter field strength is often to high to assume a... [Pg.313]

These equations are the coupled system of discrete equations that define the rigorous forward problem. Note that we can take advantage of the convolution form for indices (i — I) and (j — J). Then, by exciting the conductive media with a number N/ oi frequencies, one can obtain the multifrequency model. The kernels of the integral equations are described in [13] and [3j. [Pg.328]

The sensitive layer of the systems under investigation eonsists of a mixture of BaFBr with Eu dotation. Other systems are available in the mean time too. X-ray- or y-quants initiate transitions of electrons in the crystal lattice. Electrons are excited from the valence band to the conduction band [2]. Electrons from the conduction band are trapped in empty Br -lattice places. They can return to the valence band via the conduction band after an excitation by... [Pg.468]

Electronic and optical excitations usually occur between the upper valence bands and lowest conduction band. In optical excitations, electrons are transferred from the valence band to the conduction band. This process leaves an empty state in the valence band. These empty states are called holes. Conservation of wavevectors must be obeyed in these transitions + k = k where is the wavevector of the photon, k is the... [Pg.114]

Semiconductors are poor conductors of electricity at low temperatures. Since the valence band is completely occupied, an applied electric field caimot change the total momentum of the valence electrons. This is a reflection of the Pauli principle. This would not be true for an electron that is excited into the conduction band. However, for a band gap of 1 eV or more, few electrons can be themially excited into the conduction band at ambient temperatures. Conversely, the electronic properties of semiconductors at ambient temperatures can be profoundly altered by the... [Pg.114]

Metals are fiindamentally different from insulators as they possess no gap in the excitation spectra. Under the influence of an external field, electrons can respond by readily changing from one k state to another. The ease by which the ground-state configuration is changed accounts for the high conductivity of metals. [Pg.127]

The combination of electrochemistry and photochemistry is a fonn of dual-activation process. Evidence for a photochemical effect in addition to an electrochemical one is nonnally seen m the fonn of photocurrent, which is extra current that flows in the presence of light [, 89 and 90]. In photoelectrochemistry, light is absorbed into the electrode (typically a semiconductor) and this can induce changes in the electrode s conduction properties, thus altering its electrochemical activity. Alternatively, the light is absorbed in solution by electroactive molecules or their reduced/oxidized products inducing photochemical reactions or modifications of the electrode reaction. In the latter case electrochemical cells (RDE or chaimel-flow cells) are constmcted to allow irradiation of the electrode area with UV/VIS light to excite species involved in electrochemical processes and thus promote fiirther reactions. [Pg.1945]

Figure C1.5.12.(A) Fluorescence decay of a single molecule of cresyl violet on an indium tin oxide (ITO) surface measured by time-correlated single photon counting. The solid line is tire fitted decay, a single exponential of 480 5 ps convolved witli tire instmment response function of 160 ps fwiim. The decay, which is considerably faster tlian tire natural fluorescence lifetime of cresyl violet, is due to electron transfer from tire excited cresyl violet (D ) to tire conduction band or energetically accessible surface electronic states of ITO. (B) Distribution of lifetimes for 40 different single molecules showing a broad distribution of electron transfer rates. Reprinted witli pennission from Lu andXie [1381. Copyright 1997 American Chemical Society. Figure C1.5.12.(A) Fluorescence decay of a single molecule of cresyl violet on an indium tin oxide (ITO) surface measured by time-correlated single photon counting. The solid line is tire fitted decay, a single exponential of 480 5 ps convolved witli tire instmment response function of 160 ps fwiim. The decay, which is considerably faster tlian tire natural fluorescence lifetime of cresyl violet, is due to electron transfer from tire excited cresyl violet (D ) to tire conduction band or energetically accessible surface electronic states of ITO. (B) Distribution of lifetimes for 40 different single molecules showing a broad distribution of electron transfer rates. Reprinted witli pennission from Lu andXie [1381. Copyright 1997 American Chemical Society.
In an intrinsic semiconductor, tlie conductivity is limited by tlie tlieniial excitation of electrons from a filled valence band (VB) into an empty conduction band (CB), across a forbidden energy gap of widtli E. The process... [Pg.2877]

In a defect-free, undoped, semiconductor, tliere are no energy states witliin tire gap. At 7"= 0 K, all of tire VB states are occupied by electrons and all of the CB states are empty, resulting in zero conductivity. The tliennal excitation of electrons across tire gap becomes possible at T > 0 and a net electron concentration in tire CB is established. The electrons excited into tire CB leave empty states in tire VB. These holes behave like positively charged electrons. Botli tire electrons in the CB and holes in tire VB participate in tire electrical conductivity. [Pg.2881]


See other pages where Conducting excitations is mentioned: [Pg.41]    [Pg.858]    [Pg.59]    [Pg.2725]    [Pg.332]    [Pg.73]    [Pg.414]    [Pg.2724]    [Pg.231]    [Pg.573]    [Pg.42]    [Pg.219]    [Pg.618]    [Pg.1471]    [Pg.608]    [Pg.1470]    [Pg.41]    [Pg.858]    [Pg.59]    [Pg.2725]    [Pg.332]    [Pg.73]    [Pg.414]    [Pg.2724]    [Pg.231]    [Pg.573]    [Pg.42]    [Pg.219]    [Pg.618]    [Pg.1471]    [Pg.608]    [Pg.1470]    [Pg.64]    [Pg.76]    [Pg.255]    [Pg.272]    [Pg.298]    [Pg.368]    [Pg.506]    [Pg.717]    [Pg.419]    [Pg.114]    [Pg.115]    [Pg.125]    [Pg.134]    [Pg.1063]    [Pg.1249]    [Pg.1946]    [Pg.1982]    [Pg.2208]    [Pg.2216]    [Pg.2221]    [Pg.2873]   


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