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Cerium-doped calcium sulphide nanoparticles were synthesized using the solid state diffusion method. The formed nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-visible absorption spectroscopy and photoluminescence (PL) spectroscopy. The XRD pattern confirmed a cubic CaS phase with an average grain size of 53 nm of the formed samples. The TEM image showed non-agglomerated particles with an average size of 60 nm, which is in close agreement with the XRD result. The PL-emission spectrum showed peaks at 506 and 565 nm due to the transition from the excited state to the ground state of Ce 3+ . The effect of etching has been studied on the luminescent properties of CaS:Ce phosphors. With an increase in the etching time there is decrease in the size of the particles, as a result of which the PL spectrum showed a slight blue shift. The UV-visible absorption spectrum also showed a blue shift with an increase in etching time, which is in agreement with the nanosize effect.

We have investigated the effects of solvent used during synthesis on structural and optical properties of CdS quantum dots. Different methods of synthesis for the production of CdS quantum dots are presented. These are: (a) wet chemical co-precipitation in non-aqueous medium (i.e. methanol); (b) wet chemical co-precipitation in aqueous medium (deionized water) and (c) solid state reaction. It is demonstrated that the use of methanol as solvent leads to a strong enhancement of PL intensity of CdS quantum dots for use in optoelectronic devices. These products were characterized by X-ray powder diffraction (XRD), high resolution transmission electron microscopy (HRTEM) and scanning electron microscopy (SEM). The change in bandgap with size-quantization was investigated by UV-VIS absorption spectroscopy. CdS nanocrystals prepared in non-aqueous medium have narrow size distribution than those prepared in aqueous medium and solid state reaction. Phase transformation of CdS nanocrystals from a cubic to hexagonal structure was observed in methanol solution. The formation of CdS/Cd(OH) 2 nanostructure was also confirmed using X-ray diffraction pattern. This suggests that the strong enhancement of the PL intensity may have originated from the remarkable reduction of non-radiative recombination process, due to surface defects of quantum dots. The red shift of the Raman peaks compared to that for bulk CdS may be attributed to optical phonon confinement.

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