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Semiconductors electronic excitation

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]

Semiconductor materials are rather unique and exceptional substances (see Semiconductors). The entire semiconductor crystal is one giant covalent molecule. In benzene molecules, the electron wave functions that describe probabiUty density ate spread over the six ting-carbon atoms in a large dye molecule, an electron might be delocalized over a series of rings, but in semiconductors, the electron wave-functions are delocalized, in principle, over an entire macroscopic crystal. Because of the size of these wave functions, no single atom can have much effect on the electron energies, ie, the electronic excitations in semiconductors are delocalized. [Pg.115]

Preliminary activation may be performed not only by means of dissociation of the components being analyzed, but also by electronic and vibrational excitation, either in the gaseous phase, or even better, directly on the film of semiconductor sensor. It should be also noted that this method is applicable to dissociation in the adsorbed layer. Excitation of the molecules in adsorbed layer (we are referring to physically adsorbed particles) can be performed optically, by an electron (ion) beam, or by an electronically excited atom beam, by Hg, for example [10, 11]. [Pg.177]

From the above-made review of literature, one may infer that the interaction of metastable atoms of rare gases with a surface of semiconductors and dielectrics is studied, but little. The study of the mechanism of transferring energy of electron-excited particles to a solid body during the processes under discussion is urgent. The method of sensor detection of rare gas metastable atoms makes it possible to obtain new information about the heterogeneous de-excitation of metastable atoms inasmuch as it combines high sensitivity with the possibility to conduct measurements under different conditions. [Pg.326]

Variation of the Au/ZnO - sensor electrical conductivity under the action of RGMAs is a complicated process including a stage of restructuring the semiconductor electron subsystem due to the excitation en-... [Pg.329]

The adsorbed sensitizers in the excited state inject an electron into the conduction band of the semiconductor substrate, provided that the excited state oxidation potential is above that of the conduction band. The excitation of the sensitizer involves transfer of an electron from the metal t2g orbital to the 7r orbital of the ligand, and the photo-excited sensitizer can inject an electron from a singlet or a triplet electronically excited state, or from a vibrationally hot excited state. The electrochemical and photophysical properties of both the ground and the excited states of the dye play an important role in the CT dynamics at the semiconductor interface. [Pg.746]

No naked semiconductor photocathode has been demonstrated to have good kinetics for the evolution of H2, despite the fact that the position of Eqb in many cases has been demonstrated to be more negative than E° (H2O/H2). This means that electrons excited to the conduction band have the reducing power to effect H2 evolution, but the kinetics are too poor to compete with e - h+ recombination. The demonstration that N,N -dimethyl-4,4 -bipyridinium, MV2+, could be efficiently photoreduced at illuminated p-type Si to form MV+ in aqueous solution under conditions where E° (MV2+/+) = E° (H20/H2) when no H2 evolution occurs establishes directly that the thermodynamics are good, but the kinetics are poor, for H2 evolution.(23,47)... [Pg.76]

Electrical conductivity is due to the motion of free charge carriers in the solid. These may be either electrons (in the empty conduction band) or holes (vacancies) in the normally full valence band. In a p type semiconductor, conductivity is mainly via holes, whereas in an n type semiconductor it involves electrons. Mobile electrons are the result of either intrinsic non-stoichiometry or the presence of a dopant in the structure. To promote electrons across the band gap into the conduction band, an energy greater than that of the band gap is needed. Where the band gap is small, thermal excitation is sufficient to achieve this. In the case of most iron oxides with semiconductor properties, electron excitation is achieved by irradiation with visible light of the appropriate wavelength (photoconductivity). [Pg.115]

Brus LE (1984) Electron-electron and electron-hole interactions in small semiconductor crystallites the size dependence of the lowest electronic excited state. J Chem Phys 80 4403-4409... [Pg.252]

Electroluminescence. In Section 6.3.2.5, we saw that some materials—in particular, semiconductors—can reemit radiation after the absorption of light in a process called photoluminescence. A related type of emission process, which is common in polymer-based semiconductors, called electroluminescence, results when the electronic excitation necessary for emission is brought about by the application of an electric field rather than by incident photons. The electric field injects electrons into the conduction band, and holes into the valence band, which upon recombination emit light. [Pg.670]

The difference between amorphous and crystalline solids shows up more clearly in phonon excitations than in electronic excitations. Contributions from the entire phonon density of states appear in the first-order Raman and infrared spectra of amorphous solids. All modes in elemental amorphous semiconductors are active in the infrared. [Pg.433]

Semiconductor electrodes can be used in galvanic cells like metal electrodes and a controlled electrode potential can be applied by means of a potentiostat, if the electrode can be contacted with a suitable metal without formation of a barrier layer (ohmic contact). Suitable techniques for ohmic contacts have been worked out in connection with semiconductor electronics. Surface treatment is important for the properties of semiconductor electrodes in all kind of charge transfer processes and especially in the photoresponse. Mechanical polishing generates a great number of new electronic states underneath the surface 29> which can act as quenchers for excited molecules at the interface. Therefore, sufficient etching is imperative for studying photocurrents caused by excited dyes. [Pg.46]

If we think of dyes as intrinsic semiconductors, each excitation gives an electron-hole pair (n = p) so that in the case of a bimolecular recombination process... [Pg.90]

In d semiconductors, however, another type of electron excitation is possible, namely, the transition between two d bands, both of which correspond... [Pg.292]


See other pages where Semiconductors electronic excitation is mentioned: [Pg.1785]    [Pg.135]    [Pg.193]    [Pg.417]    [Pg.57]    [Pg.332]    [Pg.254]    [Pg.402]    [Pg.239]    [Pg.4]    [Pg.8]    [Pg.178]    [Pg.280]    [Pg.283]    [Pg.300]    [Pg.325]    [Pg.341]    [Pg.342]    [Pg.392]    [Pg.245]    [Pg.39]    [Pg.138]    [Pg.403]    [Pg.442]    [Pg.337]    [Pg.344]    [Pg.266]    [Pg.261]    [Pg.181]    [Pg.182]    [Pg.556]    [Pg.149]    [Pg.56]    [Pg.66]    [Pg.67]    [Pg.127]   
See also in sourсe #XX -- [ Pg.221 ]




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