Cadmium doped

Four different types of junctions can be used to separate the charge carriers in solar cebs (/) a homojunction joins semiconductor materials of the same substance, eg, the homojunction of a p—n sibcon solar ceb separates two oppositely doped layers of sibcon 2) a heterojunction is formed between two dissimbar semiconductor substances, eg, copper sulfide, Cu S, and cadmium sulfide, CdS, in Cu S—CdS solar cebs (J) a Schottky junction is formed when a metal and semiconductor material are joined and (4) in a metal—insulator—semiconductor junction (MIS), a thin insulator layer, generaby less than 0.003-p.m thick, is sandwiched between a metal and semiconductor material. 

Commonly used II-VI compounds include zinc sulfide, zinc selenide, zinc telluride, cadmium sulfide, cadmium telluride, and mercury cadmium telluride. These materials are not as widely used as the III-V compounds, one reason being that it is difficult to achieve p-type doping. Mercury cadmium telluride is used extensively in military night sights, which detect in the 8-13 im spectral band (a similar material, platinum silicide, is being developed for that purpose). The major applications ofCVD II-VI compounds are found in photovoltaic and electroluminescent displays. 

Karas BR, Strickert HH, Schreiner R, EUis AB (1981) Luminescent photoelectrochemical cells. 5. Multiple emission from teUurium-doped cadmium sulfide photoelectrodes and implications regarding excited-state communication. J Am Chem Soc 103 1648-1651... 

Electrodes responding to other halides, sulphide, cyanide, silver, lead, copper and cadmium are made using membranes fabricated from pure or doped silver sulphide (Ag2S). The membrane potential is affected by the movement of Ag+ ions between cationic lattice sites which in turn is determined by the activities of the Ag+ ion in the internal and sample solutions. As the activity of the former is fixed, that of the latter alone influences the membrane potential. The electrode will also respond to the presence of S2- ions because of their effect on the Ag+ ion activity via the solubility product expression ... 

Diffusion in the extrinsic region can readily be modified by doping, although knowledge of the mechanism by which the diffusion takes place is important if this is to be immediately successful. For example, sodium chloride structure materials that conduct by a vacancy mechanism can have the cation conductivity enhanced by doping with divalent cations, as these generate compensating cation vacancies. The inclusion of cadmium chloride into sodium chloride can be written ... 

Vanadium(n) Complexes.—Dehydration of VSO. THjO has been shown to proceed via the formation of VS04,mH20 (where n = 6, 4, or 1) and V(OH)-(SO4), which were characterized by X-ray studies. The polarographic behaviour and the oxidation potential of the V -l,2-cyclohexanediamine-tetra-acetic acid complex, at pH 6—12, have been determined.Formation constants and electronic spectra have been reported for the [Vlphen),] " and [V20(phen)] complexes. The absorption spectrum of V ions doped in cadmium telluride has been presented and interpreted on a crystal-field model. The unpaired spin density in fluorine 2pit-orbitals of [VF ] , arising from covalent transfer and overlap with vanadium orbitals, has been determined by ENDOR spectroscopy and interpreted using a covalent model. " ... 

Both compounds crystallize with the cadmium diiodide structure (space group P3ml) as previously reported on polycrystalline samples.3 For platinum disulfide, ao = 3.542(1) A and c0 = 5.043(1) A, and for platinum ditelluride, a0 = 4.023(1) A and c0 = 5.220(3) A. Direct chemical analysis for the component elements was not carried out. Instead, precision density and unit-cell determinations were performed to characterize the samples. The densities of both compounds as determined by a hydrostatic technique with heptadecafluorodeca-hydro-l-(trifluoromethyl)naphthalene as the density fluid4 indicated that they are slightly deficient in platinum. For platinum disulfide, = 7.86 g/cm3 and Pmeas = 7.7(1) gm/cm3, and for platinum ditelluride, p = 10.2 gm/cm3 and Pmeas = 9.8(1) gm/cm3. In a typical experiment an emission spectrum of the platinum disulfide showed that phosphorus was present in less than 5 ppm. A mass spectroscopic examination of the platinum ditelluride revealed a small doping by sulfur (less than 0.4%) and traces of chlorine and phosphorus (less than 100 ppm). 

No structural data are available for silver(H) pyridine salts. Based on the evidence500 of ease of doping at all levels of the silver and copper persulfate complexes into the cadmium spedes, isomorphism was assumed. X-Ray powder photographs have since shown this not to be the case.499... 

Effects of Temperature on Excited-State Descriptions of Luminescent Photoelectrochemical Cells Employing Tellurium-Doped Cadmium Sulfide Electrodes... 

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