Aqueous solution, nanoparticles

CuNPs) in Fig. 7 shows the monodisperse and uniformly distributed spherical particles of 10+5 nm diameter. The solution containing nanoparticles of silver was found to be transparent and stable for 6 months with no significant change in the surface plasmon and average particle size. However, in the absence of starch, the nanoparticles formed were observed to be immediately aggregated into black precipitate. The hydroxyl groups of the starch polymer act as passivation contacts for the stabilization of the metallic nanoparticles in the aqueous solution. The method can be extended for synthesis of various other metallic and bimetallic particles as well. 

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. 

A. and Angel O. Z. (2008). Synthesis and spectral properties of starch capped CdS nanoparticles in aqueous solution J. Cryst. Growth, 310,160-164. 

The photoelectrochemical properties of CdS nanoparticles formed in LB films of cadmium arachidate on ITO glass (indium tin oxide-coated glass) were investigated [188]. The CdS particles were formed by exposure to H2S gas, and then the cadmium arachidate structure was regenerated by exposing the gas-treated films with aqueous solutions of CdCL. Gassing/immersion cycling increased the particle size from 2.3 0.7 nm after one cycle to 9.8 2.4 nm after five cycles. The 9.8-nm particles showed UV-visible ab-... 

Another method to synthesize hollow nanocapsules involves the use of nanoparticle templates as the core, growing a shell around them, then subsequently removing the core by dissolution [30-32]. Although this approach is reminiscent of the sacrificial core method, the nanoparticles are first trapped and aligned in membrane pores by vacuum filtration rather than coated while in aqueous solution. The nanoparticles are employed as templates for polymer nucleation and growth Polymerization of a conducting polymer around the nanoparticles results in polymer-coated particles and, following dissolution of the core particles, hollow polymer nanocapsules are obtained. 

Herein we briefly mention historical aspects on preparation of monometallic or bimetallic nanoparticles as science. In 1857, Faraday prepared dispersion solution of Au colloids by chemical reduction of aqueous solution of Au(III) ions with phosphorous [6]. One hundred and thirty-one years later, in 1988, Thomas confirmed that the colloids were composed of Au nanoparticles with 3-30 nm in particle size by means of electron microscope [7]. In 1941, Rampino and Nord prepared colloidal dispersion of Pd by reduction with hydrogen, protected the colloids by addition of synthetic pol5mer like polyvinylalcohol, applied to the catalysts for the first time [8-10]. In 1951, Turkevich et al. [11] reported an important paper on preparation method of Au nanoparticles. They prepared aqueous dispersions of Au nanoparticles by reducing Au(III) with phosphorous or carbon monoxide (CO), and characterized the nanoparticles by electron microscopy. They also prepared Au nanoparticles with quite narrow... 

Vinodgopal et al. prepared Pt/Ru bimetallic nanoparticles by sonochemical reduction of Pt(II) and Ru(III) in aqueous solutions. TEM images indicated that sequential reduction of the Pt(II) followed by the Ru(III) produced Pt-core/Ru-shell bimetallic nanoparticles. In the presence of sodium dodecyl sulfate (SDS), as a stabilizer, the nanoparticles had diameters between 5 and 10 nm. When PVP was used as the stabilizer, the rate of reduction is much faster, giving ultrasmall bimetallic nanoparticles of ca. 5nm diameter [141]. 

In order to obtain Pt nanoparticles, aqueous solution of 10 M K2PtCl4, which contained 10 M (as monomer unit) of poly-NIPA or poly-NEA, was bubbled with Ar gas and then H2 gas. Then the reaction vessel was sealed tightly and kept in a water bath at a suitable temperature. At given reaction times, the vessels were opened and the samples for transmission electron microscopy (TEM) were prepared by soaking a grid (carbon substrate, Oken) in the colloidal solution and then drying it in the air. The TEM (Hitachi H-8100) was operated at 200 kV. 

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