A pulsed laser-assisted in liquid environment method has been developed successfully to synthesize size-tunable (5–12 nm) and different shapes (sphere, rod, rope) of nano II–VI semiconductor (cadmium sulfide). This method can be carried out in two ways; the first one is the top-down technique, which has been discussed in publications in the last few decades, and the other one is the bottom-up technique, which appears for the first time in this paper. X-ray diffraction, ultraviolet-visible spectroscopy, and transmission electron microscopy confirm that the nanoparticles are crystalline. The methods lead to the production of nanomaterials, which are important for photonics and biosensing applications. Both synthesized methods can be applied in all materials because of their ability to ablate almost all kinds of materials due to the ultrahigh energy density and control over the growth process by manipulating the process parameters such as intensity, wavelength, and so on.

We study numerically the optical properties of low-buckled silicene and AB-stacked bilayer graphene quantum dots subjected to an external electric field, which is normal to their surface. Within the tight-binding model, the optical absorption is calculated for quantum dots, of triangular and hexagonal shapes, with zigzag and armchair edge terminations. We show that in triangular silicene clusters with zigzag edges a rich and widely tunable infrared absorption peak structure originates from transitions involving zero energy states. The edge of absorption in silicene quantum dots undergoes red shift in the external electric field for triangular clusters, whereas blue shift takes place for hexagonal ones. In small clusters of bilayer graphene with zigzag edges the edge of absorption undergoes blue/red shift for triangular/hexagonal geometry. In armchair clusters of silicene blue shift of the absorption edge takes place for both cluster shapes, while red shift is inherent for both shapes of the bilayer graphene quantum dots.