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Banded structures liquid

Cathodoluminescence microscopy and spectroscopy techniques are powerful tools for analyzing the spatial uniformity of stresses in mismatched heterostructures, such as GaAs/Si and GaAs/InP. The stresses in such systems are due to the difference in thermal expansion coefficients between the epitaxial layer and the substrate. The presence of stress in the epitaxial layer leads to the modification of the band structure, and thus affects its electronic properties it also can cause the migration of dislocations, which may lead to the degradation of optoelectronic devices based on such mismatched heterostructures. This application employs low-temperature (preferably liquid-helium) CL microscopy and spectroscopy in conjunction with the known behavior of the optical transitions in the presence of stress to analyze the spatial uniformity of stress in GaAs epitaxial layers. This analysis can reveal,... [Pg.156]

SoUd ice forms a crystal of diamond structure, in which one water molecule is hydrogen-bonded with four adjacent water molecules. Most (85%) of the hydrogen bonds remain even after solid ice melts into liquid water. The structure of electron energy bands of liquid water (hydrogen oxide) is basically similar to that of metal oxides, 6dthough the band edges are indefinite due to its amorphous structure. [Pg.45]

The appearance of the IR spectrum of a compound depends somewhat on the sample s phase. Under high resolution, gas-phase IR bands consist of closely spaced lines—the rotational fine structure however, IR bands of liquids and solids very rarely show rotational fine structure. In most solids, the molecules are held in fixed lattice positions and are not free to rotate. In liquids, the high rate of intermolecular collisions and the substantial intermolecular interactions cause random shifts in the rotational energies, thereby broadening the rotational lines of a band sufficiently to merge them into one another, and eliminate the rotational fine structure. (Broadening of fine structure lines is also observed in gas-phase spectra when the pressure is increased.)... [Pg.386]

Interfacial electron transfer across a solid-liquid junction can be driven by photoexcitation of doped semiconductors as single crystals, as polycrystalline masses, as powders, or as colloids. The band structure in semiconductors (281) makes them useful in photoelectrochemical cells. The principles involved in rendering such materials effective redox catalysts have been discussed extensively (282), and will be treated here only briefly. [Pg.294]

It is experimentally easy to generate Raman spectra using polarized light and to observe the partial depolarization of the spectra. Bands of totally symmetric vibrations are strongly polarized in liquid or solution spectra. All other bands in liquid or solution are depolarized. Polarization effects are essential to elucidate structures, but are usually ignored in most other applications. Details of the theory and experimental procedure can be found in the literature (15,16). [Pg.208]

In mixtures water and solvents with lone pair electrons, the structure depends on the base strength of the lone pair electrons in the series given on page 9. For example the spectra of water-dioxan (Fig. 14) show a weaker frequency shift in comparison with water-alcohol mixtures (Fig. 12) — that means weaker H-bonds — of the H-bond band of water (1.92 q instead 1.94 /a). The wavelength 1.896 ju in Fig. 14 of the non H-bonded OH band instead 1.89 ju in water/methanol (Fig. 12) corresponds with a non H-bonded water OH group whose second OH is H-bonded (Compare the free OH band in liquid water 200 °C < T< 350° in Fig. 1249 ). [Pg.136]

Figure 1. Band Structure in a n-type Semiconductor A. Solid State. B. In contact with a liquid phase redox couple (0/R). IL=energy of the conduction band. Vertical line indicates solid-liquid interface. CB= conduction band VB = valence band. Figure 1. Band Structure in a n-type Semiconductor A. Solid State. B. In contact with a liquid phase redox couple (0/R). IL=energy of the conduction band. Vertical line indicates solid-liquid interface. CB= conduction band VB = valence band.
Before and after the works described above, contributions to the design and fabrication of similar multicomponent films or gels of cholesteric character, mainly based on HPC, EC, or their derivatives were also made [202, 219-224], Some of these [219,220,224] dealt with shear-deformed network systems preserving a unique banded structure, so that the disappearance and recovery of the optical anisotropy could be controlled thermo-reversibly. Special mention should be made of the successful preparation of two novel classes of solid materials maintaining cholesteric liquid-crystalline order. One consists of essentially pure cellulose only, and the other is a ceramic silica with an imprint of cellulosic chiral mesomorphy. [Pg.139]

Figure 5.5.9-2 The energy band structures of the Rhodonines in the liquid crystalline state with the relevant profiles and the associated difference in energy profile that describes the molecular absorption spectrum of the molecules when in the liquid crystalline state. See text. Figure 5.5.9-2 The energy band structures of the Rhodonines in the liquid crystalline state with the relevant profiles and the associated difference in energy profile that describes the molecular absorption spectrum of the molecules when in the liquid crystalline state. See text.
Figure 5.5.9-2 The energy band structures of the Rhodonines in the liquid crystalline state. 72... Figure 5.5.9-2 The energy band structures of the Rhodonines in the liquid crystalline state. 72...
Xu B-C, Stratt RM. Liquid theory for band structure in a liquid. II. p Orbitals and phonons. J Chem Phys 1990 92 1923-1935. [Pg.598]

Semi-conductors have conducting properties between those of insulators and conductors. The band structures of conductors, intrinsic semiconductors and insulators are represented schematically in Figure 1.4. The widths and the separations of the bands are dependent upon the intemuclear spacings of the constituents, so that the band structure may be modified in the vicinity of the surfaces of the crystal, by the occurrence of surface reactions, or by interactions with gases, liquids or other solids. [Pg.19]

This approximation for Exc [ ] has proved to be remarkably successful, even when applied to systems that are quite different from the electron liquid that forms the reference system for the LDA. For many decades the LDA has been applied in, e.g., calculations of band structures and total energies in solid-state physics. In quantum chemistry, it is much less popular because it fails to provide results that are accurate enough to permit a quantitative discussion... [Pg.82]

Without going into the details of energy band structure of a liquid solution, we shall note only that this structure can probably be described by the theory of disordered semiconductors (see, e. g. [Pg.155]

Fig. 5.2. a) Static structure factor of an amorphous or liquid metal b) band-structure characteristic c) pseudopotential d) perturbation characteristic for two different Fermi-sphere diameters, a-c are qualitatively drawn in arbitrary units... [Pg.167]


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