Sulfide oxidation, semiconductor

Cadmium sulfide (CdS), 2.4 eV bandgap, is one of the most widely studied non-oxide semiconductors. For a semiconductor irradiated by photons with energy equal to or greater than its bandgap, an electron from the valence band jumps to the conduction band leaving a positively charged hole behind in the valance band for CdS this is expressed as... 

Many metal oxides and sulfides exhibit semiconductor properties by virtue of their nonstoichiometry. In Section 5.3, we distinguished positive (p-type) and negative (n-type) semiconductors. 

Minerals, electrochemistry of — Many minerals, esp. the ore minerals (e.g., metal sulfides, oxides, selenides, arsenides) are either metallic conductors or semiconductors. Because of this they are prone to undergo electrochemical reactions at solid solution interfaces, and many industrially important processes, e.g., mineral leaching and flotation involve electrochemical steps [i-ii]. Electrochemical techniques can be also used in quantitative mineral analysis and phase identification [iii]. Generally, the surface of minerals (and also of glasses) when in contact with solutions can be charged due to ion-transfer processes. Thus mineral surfaces also have a specific point of zero charge depending on their sur-... 

Nevertheless, the first functional working TFT was demonstrated by Weimer in 1962 (Ref 2). He used thin films of polycrystalline cadmium sulfide, similar to those ones developed for photodetectors. The simplified structure is shown in Fig. 1(b). Other TFT semiconductor materials like CdSe, Te, InSb and Ge were investigated, but in the mid-1960 s the emergence of the metal oxide semiconductor field effect transistor (MOSFET) based on the crystalline silicon technology and the possibility to perform integrated circuits, led to a decline in TFT development activity by the end of the 1960s. 

Consider that atoms have a size range of about 1-2 A. Most inorganic solids, with the exception of halides, sulfides (and other pnictides), are based upon the oxygen atom, i.e.- oxide = O", whose atomic radius does not change even when sulfates, phosphates and silicates are formed. Oxide has an atomic diameter of 1.5 A or 0.15 nm. = 0.00015 (om. Nanoparticles are clumps of 1000 to 10,000 atoms. The latter would be a particle of 0.15 (om. in diameter. They can be metal oxides, semiconductors, or metals with novel properties useful for electronic, optical, magnetic and/or catalytic uses. 

Oxidation of some sulfides by semiconductor photocatalysis produces high yields of sulfoxides [Eq. (15)] [122]. It is proposed that the radical cation of the sulfide reacts with oxygen, and then undergoes elimination to yield the sulfoxide. The reaction efficiency of substituted aryl sulfides can be enhanced by an electron-donating substituent in the order of OCH3 > CH3 > H > Cl, Br. 

Sulfide oxidation can also be driven photo-electrochemically, using photon absorption at suitable semiconductors to generate electron-hole pairs [29, 30], the latter oxidizing sulfide ions by reaction (24) ... 

Heterogeneous Photocatalysis. Heterogeneous photocatalysis is a technology based on the irradiation of a semiconductor (SC) photocatalyst, for example, titanium dioxide [13463-67-7] Ti02, zinc oxide [1314-13-2] ZnO, or cadmium sulfide [1306-23-6] CdS. Semiconductor materials have electrical conductivity properties between those of metals and insulators, and have narrow energy gaps (band gap) between the filled valence band and the conduction band (see Electronic materials Semiconductors). 

Bina Selenides. Most biaary selenides are formed by beating selenium ia the presence of the element, reduction of selenites or selenates with carbon or hydrogen, and double decomposition of heavy-metal salts ia aqueous solution or suspension with a soluble selenide salt, eg, Na2Se or (NH 2S [66455-76-3]. Atmospheric oxygen oxidizes the selenides more rapidly than the corresponding sulfides and more slowly than the teUurides. Selenides of the alkah, alkaline-earth metals, and lanthanum elements are water soluble and readily hydrolyzed. Heavy-metal selenides are iasoluble ia water. Polyselenides form when selenium reacts with alkah metals dissolved ia hquid ammonia. Metal (M) hydrogen selenides of the M HSe type are known. Some heavy-metal selenides show important and useful electric, photoelectric, photo-optical, and semiconductor properties. Ferroselenium and nickel selenide are made by sintering a mixture of selenium and metal powder. 

The cadmium chalcogenide semiconductors (qv) have found numerous appHcations ranging from rectifiers to photoconductive detectors in smoke alarms. Many Cd compounds, eg, sulfide, tungstate, selenide, teUuride, and oxide, are used as phosphors in luminescent screens and scintiUation counters. Glass colored with cadmium sulfoselenides is used as a color filter in spectroscopy and has recently attracted attention as a third-order, nonlinear optical switching material (see Nonlinear optical materials). DiaLkylcadmium compounds are polymerization catalysts for production of poly(vinyl chloride) (PVC), poly(vinyl acetate) (PVA), and poly(methyl methacrylate) (PMMA). Mixed with TiCl, they catalyze the polymerization of ethylene and propylene. 

The sulfides have been less thoroughly examined than the oxides but it is clear that a number of stable phases can be produced and nonstoichiometry is again prevalent (p. 679). The most important are the disulfides, which are semiconductors with metallic lustre. TiS2 and ZrS2 have the Cdl2 structure (p. 1211) in which the cations occupy the octahedral sites between alternate layers of hep anions. 

On the basis of our theoretical considerations and preliminary experimental work, it is hoped that fast processes of charge carriers will become directly measurable in functioning photoelectrochemical cells, Typical semiconductor electrodes are not the only systems accessible to potential-dependent microwave transient measurements. This technique may also be applied to the interfacial processes of semimetals (metals with energy gaps) or thin oxide or sulfide layers on ordinary metal electrodes. 

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