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Concentration of defect

Two point defects may aggregate to give a defect pair (such as when the two vacanc that constitute a Schottky defect come from neighbouring sites). Ousters of defects ( also form. These defect clusters may ultimately give rise to a new periodic structure oi an extended defect such as a dislocation. Increasing disorder may alternatively give j to a random, amorphous solid. As the properties of a material may be dramatically alte by the presence of defects it is obviously of great interest to be able to imderstand th relationships and ultimately predict them. However, we will restrict our discussion small concentrations of defects. [Pg.639]

The success has been primarily due to the developments that occurred in the eady 1970s (3) at the University of Dundee (United Kingdom) where it was demonstrated that a device-quaUty amorphous siUcon semiconductor (i -Si) could be produced with the following features low concentration of defects, high photosensitivity, abiUty to be doped, and no size limitation. [Pg.357]

Although vitreous siUca is a simple, single-component glass, its properties can vary significantly, depending on thermal history, the type and concentration of defects, and impurities. Vitreous siUca can, however, be one of the purest commercially available glassy materials. In synthetic vitreous sihcas, for example, total metal contamination is typically measured ia the 50—100 ppb range. Even at such a low level of impurities, differences ia properties, such as uv-transmission, are observed for various siUcas. [Pg.497]

It is not necessary for a compound to depart from stoichiometry in order to contain point defects such as vacant sites on the cation sub-lattice. All compounds contain such iirndirsic defects even at the precisely stoichiometric ratio. The Schottky defects, in which an equal number of vacant sites are present on both cation and anion sub-lattices, may occur at a given tempe-ramre in such a large concentration drat die effects of small departures from stoichiometry are masked. Thus, in MnOi+ it is thought that the intrinsic concentration of defects (Mn + ions) is so large that when there are only small departures from stoichiometry, the additional concentration of Mn + ions which arises from these deparmres is negligibly small. The non-stoichiometry then varies as in this region. When the departure from non-stoichio-... [Pg.228]

The critical size of the stable nucleus at any degree of under cooling can be calculated widr an equation derived similarly to that obtained earlier for the concentration of defects in a solid. The configurational entropy of a mixture of nuclei containing n atoms widr o atoms of the liquid per unit volume, is given by the Boltzmann equation... [Pg.299]

Asay and Gupta [25] measure elastic precursor amplitudes as functions of propagation distance for two different divalent impurity concentrations in <100)-loaded LiF. It is shown that not only does the presence of divalent ions affect the precursor amplitude, but also that the state of the dispersion plays an important part. It is concluded that, for a given concentration of defects, the rate of precursor attenuation is reduced if the defects are clustered. [Pg.228]

If n is the concentration of defects (cation vacancies or positive holes) at equilibrium, then, applying the law of mass action to equation 1.157... [Pg.245]

The exact situation with ZnO is not altogether clear. Under most experimental conditions it seems that equation 1.163 is the important reaction, but equation 1.164 cannot be ignored at high temperatures. Applying the mass-action formula to equation 1.163 we have for n, the concentration of defects (interstitial Zn ions or free electrons)... [Pg.247]

Investigations based on equation (a) are indirect. Direct structural studies using diffraction techniques (X-ray or neutron), or electron microscopy, while they cannot detect the low concentrations of defects present in NiO or CoO are indispensible to the study of grossly non-stoichiometric oxides like FeO, TiOj, WOj etc., and particularly electron microscopes with a point-to-point resolution of about 0.2 nm are widely used. The first direct observation of a point defect (actually a complex of two interstitial metal atoms, and two oxygen atoms in Nb,2029) was made" using electron microscopy. [Pg.252]

This formula for ki can be cast into another form by using equations 1.169 and 1.170. We note first that in these latter equations K is the concentration of defects in CujO at 1 atm pressure of oxygen, so that (A ),Q) is the self-diffusion coefficient of Cu in CujO at this oxygen pressure. Call this self-diffusion coefficient Z7 , then... [Pg.258]

The equilibrium concentration of defects is obtained by applying the law of mass action to Eq. (7) or (8). This leads in the case of Frenkel disorder to... [Pg.529]

Let us now consider the concentration of defects that might appear in the MXs crystal. [Pg.107]

Therefore, the detailed analysis of concentration of defects in surface-adjacent layer and in the volume of adsorbent as well as assessment of the values of diffusion coefficients of defects and particles of various gases in material of adsorbent are very important for understanding the processes of both reversible and irreversible change in electrophysical characteristics of semiconductor during low temperature (if compared to the temperature of creation of defects) interaction with gaseous phase. [Pg.86]

We should note that expressions (2.21) and (2.27) were obtained in application to a specific bridge of the open type characterized by thickness h and initial concentration of superstoichiometric metal [Me ]o- In real polycrystal with dominant fraction of bridges of this very type there is a substantial spread with respect to the thickness of bridges and to concentration of defects. Therefore, the local electric conductivity of the material in question is a random value of statistical ohmic subgrid formed by barrier-free contacts of microoystals. [Pg.127]

Therefore, the kinetics of generation of defects in surface-adjacent layers is similar to kinetics of emission of O-atoms. (The estimates indicate that the maximum concentration of vacancies in this case may attain the value of 10 for a sample with area 1 cm ). If one assumes that the emission of oxygen atoms is caused by processes of annihilation of vacancies in the sample, then the coincidence in time dependence of stationary concentration of defects can be indicative that these processes are limited by generation of defects, which, in its turn, is controlled by processes of formation of oxide phase in surface-adjacent silver layers. Oxidation, especially at initial stage, is characterized by intensive formation of defects [54]. [Pg.377]

It is obvious that during deformation of the sample due to mechanical loading the creation and annihilation defects will also take place. Similar to preceding experiments in this case the value of deformation would determine the concentration of defects. However, in case of mechanical loading the defects will be evenly spread over the whole volume of samples, whereas in case of silver oxidation they remain localized only in the surface-adjacent layers. Therefore, emission of oxygen atoms under conditions of mechanical deformation of samples in oxygen atmosphere has low probability due to intensive annihilation of defects in surface-adjacent layers. Special experiments confirmed this conclusion. [Pg.379]

Stereodefects reduce the overall regularity of an isotactic polymer chain and hinder its ability to crystallize. As the concentration of defects increases, the degree of crystallinity falls, resulting in reduced density, reduced melting temperatures, lower heat distortion temperatures, reduced modulus, and reduced yield stress. [Pg.105]

Displacements of lattice members are determined by energy factors and concentration gradients. To a considerable extent, diffusion in solids is related to the existence of vacancies. The "concentration" of defects, N0, (sites of higher energy) can be expressed in terms of a Boltzmann distribution as... [Pg.279]

Fig. 9.lld). The up-conversion spectrum consists of three major peaks (Fig. 9.18). [All up-conversion spectra from Er3+ (including those using energy transfer, below) are similar, but the relative intensities of the three peaks vary with concentration of defects and the host matrix.]... [Pg.424]


See other pages where Concentration of defect is mentioned: [Pg.395]    [Pg.352]    [Pg.354]    [Pg.395]    [Pg.117]    [Pg.228]    [Pg.122]    [Pg.71]    [Pg.166]    [Pg.167]    [Pg.168]    [Pg.197]    [Pg.326]    [Pg.109]    [Pg.162]    [Pg.115]    [Pg.457]    [Pg.426]    [Pg.441]    [Pg.235]    [Pg.108]    [Pg.128]    [Pg.258]    [Pg.281]    [Pg.58]    [Pg.228]    [Pg.227]    [Pg.235]    [Pg.236]    [Pg.260]    [Pg.40]   
See also in sourсe #XX -- [ Pg.45 , Pg.191 , Pg.383 , Pg.394 , Pg.566 ]




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Concentration of intrinsic defects

Defect Concentration as a Function of Temperature and Pressure

Equilibrium Concentration of Frenkel Defects Derived from Configurational Entropy

Equilibrium Concentration of Schottky Defects Derived from Configurational Entropy

Two-Dimensional Representations of Defect Concentrations

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