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Silver chloride, crystal defects

Despite the fact that not all details of the photographic process are completely understood, the overall mechanism for the production of the latent image is well known. Silver chloride, AgBr, crystallizes with the sodium chloride structure. While Schottky defects are the major structural point defect type present in most crystals with this structure, it is found that the silver halides, including AgBr, favor Frenkel defects (Fig. 2.5). [Pg.59]

Lattice defects in ionic crystals are interstitial ions and ion vacancies. In crystalline sodium chloride NaCl a cation vacancy Vn - is formed by producing a surface cation NaJ, (Nal - NaJ + Vua ) this is called the Schottky defect. On the other hand, in crystalline silver chloride AgCl a pair of cation vacancy Va,. and interstitial cation Ag is formed, (Ag - Agj + ) this is called the Frenkel... [Pg.74]

Calculate the number of Frenkel defects present in a crystal of silver chloride, AgCl, at 300 K, given that the material has a cubic unit cell of edge 0.555 nm that contains four silver atoms. Assume that the interstitial atoms occupy any of eight tetrahedral sites in the unit cell. The enthalpy of formation of a Frenkel defect in AgCl is 2.69 x 10 J. [Pg.89]

The majority of inorganic systems reported to exhibit photochromism are solids, examples being alkali and alkaline earth halides and oxides, titanates, mercuric chloride and silver halides.184 185 The coloration is generally believed to result from the trapping of electrons or holes by crystal lattice defects. Alternatively, if the sample crystal is doped with an impurity capable of existing in variable oxidation states (i.e. iron or molybdenum), an electron transfer mechanism is possible. [Pg.410]

The ionic charge carriers in ionic crystals are the point defects.1 2 23,24 They represent the ionic excitations in the same way as H30+ and OH-ions are the ionic excitations in water (see Fig. 1). They represent the chemical excitation upon the perfect crystallographic structure in the same way as conduction electrons and holes represent electronic excitations upon the perfect valence situation. The fact that the perfect structure, i.e., ground structure, of ionic solids is composed of charged ions, does not mean that it is ionically conductive. In AgCl regular silver and chloride ions sit in deep Coulomb wells and are hence immobile. The occurrence of ionic conductivity requires ions in interstitial sites, which are mobile, or vacant sites in which neighbors can hop. Hence a superionic dissociation is necessary, as, e.g. established by the Frenkel reaction ... [Pg.5]


See other pages where Silver chloride, crystal defects is mentioned: [Pg.665]    [Pg.446]    [Pg.420]    [Pg.174]    [Pg.103]    [Pg.141]    [Pg.209]    [Pg.12]    [Pg.265]    [Pg.4]    [Pg.207]    [Pg.367]    [Pg.419]   
See also in sourсe #XX -- [ Pg.12 , Pg.13 ]




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