The modified thermal treatment method via alternate oxygen and nitrogen flow was successfully employed to synthesize very narrow and pure Ag nanoparticles. The structural and optical properties of the obtained metal nanoparticles at different calcination temperatures between 400 and 800 °C were studied using various techniques. The FTIR and EDX confirmed the formation of Ag nanoparticles without a trace of impurities. The XRD spectra revealed that the amorphous sample at 30 °C had transformed into the cubic crystalline nanostructures at the calcination temperature of 400 °C and higher. The TEM images showed the formation of spherical Ag nanoparticles in which the average particle size decreased with increasing calcination temperature from 7.88 nm at 400 °C to 3.29 nm at 800 °C. The optical properties were determined by UV-vis absorption spectrophotometer, which showed an increase in the conduction band of Ag nanoparticles with increasing calcination temperature from 2.75 eV at 400 °C to 3.04 eV at 800 °C. This was due to less attraction between conduction electrons and metal ions as the particle size decreases in corresponding to fewer numbers of atoms that made up the metal nanoparticles.

Very narrow and pure silver nanoparticles were synthesized by modified thermal treatment method via oxygen and nitrogen flow in succession. The structural and optical properties of the calcined silver nanoparticles at 600°C with diverse Poly(vinylpyrrolidone) concentrations varied from 2% to 4% were studied by means of different techniques. Fourier transform infrared spectroscopy was used to monitor the production of pure Ag nanoparticles at a given Poly(vinylpyrrolidone) concentration. The X-ray powder diffraction spectra are evidence for the transformation of the amorphous sample at 30°C to the cubic crystalline nanostructures at the calcination temperatures for all Poly(vinylpyrrolidone) concentrations. The transmission electron microscopy images showed the creation of spherical silver nanoparticles with the average particle size decreased by increasing Poly(vinylpyrrolidone) concentrations from 4.61 nm at 2% to 2.49 nm at 4% Poly(vinylpyrrolidone). The optical properties were investigated by means of UV–vis absorption spectrophotometer, which showed an increase in the conduction band of Ag nanoparticles with increasing Poly(vinylpyrrolidone) concentrations from 2.83 eV at 2% Poly(vinylpyrrolidone) to 2.94 eV at 4% Poly(vinylpyrrolidone) due to decreasing particle size. This was due to less attraction between conduction electrons and metal ions for smaller particle size corresponding to fewer atoms that made up the metal nanoparticles.

The purpose of this research is to examine how the electro-optical behavior of platinum (Pt) nanoparticles prepared via the gamma radiolysis process is related to both the radiation dose and to the Pt precursor concentration. The Pt precursor used in these experiments has been radiolytically degraded using a ⁶⁰Co gamma source at dosages ranging from 80 kGy to 120 kGy. As well, varying the concentration of the Pt precursor from 5.0 × 10⁻⁴ M to 20.0 × 10⁻⁴ M was carried out as a systematic investigation. Spectrophotometric analysis utilizing UV–Visible spectroscopy and TEM provided the optical data and particle size information for the nanoparticles. The results indicate that increasing the radiation dosage results in smaller Pt nanoparticle sizes due to an increased rate of nucleation and that increasing the Pt precursor concentration leads to larger Pt nanoparticles due to an increase in ion recombination. Both the dose and concentration dependency of the optical absorption spectrum indicate a significant relationship between size and plasmon behavior. Also, the conduction band energy level, which was determined from the maximum of the UV–Visible absorption peak, is dependent on the particle size and shows a pronounced quantum confinement effect, with the conduction band energy increasing as the particle size decreases. Thus, these studies provide a definitive correlation of structure–property in Pt nanoparticles and confirm the capability of the gamma radiolytic synthesis process to be used for controlling the specific electronic and optical properties of Pt nanoparticles.