Selenides cadmium CdSe

Botti and Marques addressed this problem for two experimentally synthesized cadmium selenide nanoparticles (CdSe)33 and (CdSe)34. For these clusters, the X-ray analysis showed a coordination number between 3 and 4 for the selenium atoms, which gave rise to the assumption of a cage-like structure. These cage structures are significantly different from structures that are derived from the wurtzite crystal structure, where the resulting particles are rather compact. So far, there has not been any experimental proof of the existence of such CdSe cages. 

Figure 7.1. Nanometer-sized cadmium selenide sulfide (CdSe Sj.J and cadmium selenide (CdSe). When the samples are irradiated with ultraviolet light (X = 365 nm), the emission colors range from violet to orange (right).

Karamanis, R, Maroulis, G., 8c Pouchan, C. (2006a). Basis set and electron correlation effects in all-electron ab initio calculations of the static dipole polarizability of small cadmium selenide clusters, (CdSe) , n = 1,2,3,4. Chemical Physics, 331(1), 19-25. 

Chalcogenides of Cd are similar to those of Zn and display the same duality in their structures. The sulfide and selenide are more stable in the hexagonal form whereas the telluride is more stable in the cubic form. CdS is the most important compound of cadmium and, by addition of CdSe, ZnS, HgS, etc., it yields thermally stable pigments of brilliant colours from pale yellow to deep red, while colloidal dispersions are used to colour transparent glasses. 

Light detectors fall into two categories photoconductors and photodetectors. Photoconductors are devices whose resistance decreases upon exposure to light. Cadmium sulfide (CdS) and cadmium selenide (CdSe) are the most commonly used photoconductor materials in the visible spectrum. They are still mostly produced by sputtering but CVD is used increasingly (see Ch. 12, Sec. 4.0). 

The synthetic approach is very simple and does not require any special set up. In a typical room temperature reaction, 1.0 mL aqueous solution of cadmium chloride was added to 20 mL aqueous solution of soluble starch in a 50 mL one-necked round-bottom flask with constant stirring at room temperature. The pH of the solution was adjusted from 6 to 11 using 0.1 M ammonia solution. This was followed by a slow addition of 1.0 mL colourless selenide ion stock solution. The mixture was further stirred for 2 h and aged for 18 h. The resultant solution was filtered and extracted with acetone to obtain a red precipitate of CdSe nanoaprticles. The precipitate was washed several times and dried at room temperature to give a material which readily dispersed in water. The same procedure was repeated for the synthesis of PVA and PVP - capped CdSe nanoparticles by replacing the starch solution with the PVA and PVP polymers while the synthesis of elongated nanoparticles was achieved by changing the Cd Se precursor ratio from 1 1 to 1 2. The synthesis of polymer capped ZnSe nanoparticles also follows the same procedure except that ZnCb solution was used instead of CdCb solution. 

Cathodic electrodeposition of microcrystalline cadmium-zinc selenide (Cdi i Zn i Se CZS) films has been reported from selenite and selenosulfate baths [125, 126]. When applied for CZS, the typical electrocrystallization process from acidic solutions involves the underpotential reduction of at least one of the metal ion species (the less noble zinc). However, the direct formation of the alloy in this manner is problematic, basically due to a large difference between the redox potentials of and Cd " couples [127]. In solutions containing both zinc and cadmium ions, Cd will deposit preferentially because of its more positive potential, thus leading to free CdSe phase. This is true even if the cations are complexed since the stability constants of cadmium and zinc with various complexants are similar. Notwithstanding, films electrodeposited from typical solutions have been used to study the molar fraction dependence of the CZS band gap energy in the light of photoelectrochemical measurements, along with considerations within the virtual crystal approximation [128]. 

Many colored pigments are based on cadmium compounds. For instance, cadmium sulfide (CdS) and cadmium selenide (CdSe) are used as pigments when a durable, nonfading color is required. Red is produced by CdSe, and bright yellow is produced by CdS. 

Gobet and Matijevic (17) produced monodisperse submicrometer-size particles of cadmium selenide (CdSe) and lead selenide (PbSe) by reversible release of selenide ions from selenourea in solutions of the corresponding metal salts. The equilibrium between selenourea and selenide ions is written as follows ... 

The next five chapters deal with deposition of specific groups of semiconductors. In Chapter 4, II-VI Semiconductors, all the sulphides, selenides, and (what little there is on) tellurides of cadmium (most of the chapter), zinc (a substantial part), and mercury (a small part). (Oxides are left to a later chapter.) This chapter is, understandably, a large one, due mainly to the large amount of work carried out on CdS and to a lesser extent on CdSe. Chapter 5, PbS and PbSe, provides a separate forum for PbS and PbSe, which provided much of the focus for CD in earlier years. The remaining sulphides and selenides are covered in Chapter 6, Other Sulphides and Selenides. There are many of these compounds, thus, this is a correspondingly large chapter. Chapter 7, Oxides and Other Semiconductors, is devoted mainly to oxides and some hydroxides, as well as to miscellaneous semiconductors that have only been scantily studied (elemental selenium and silver halides). These previous chapters have been limited to binary semiconductors, made up of two elements (with the exception of elemental Se). Chapter 8, Ternary Semiconductors, extends this list to semiconductors composed of three elements, whether two different metals (most of the studies) or two different chalcogens. 

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