No abstract

Transition-metal dichalcogenide quantum dots (TMDQDs) with few layers are in the forefront of recent research on tailored 2D layered materials owing to their unique band structure. Such quantum dots (QDs) draw wide interest as potential candidates for components in optoelectronic devices. Although a few attempts towards single step synthesis of MoS QDs have been demonstrated, limited methods are available for WS QDs. Herein, we demonstrate a one-step electrochemical synthesis of luminescent WS QDs from their bulk material. This is achieved by a synergistic effect of perchlorate intercalation in non-aqueous electrolyte and the applied electric field. The average size of the WS QDs is 3  ±1 nm (N=102) with few layers. The QDs show a higher photoluminescence (PL) quantum efficiency (5 %) and exhibit an excitation wavelength-dependent photoluminescence. This unprecedented electrochemical avenue offers a strategy to synthesize size tunable WS nanostructures, which have been systematically investigated by various characterization techniques such as transmission electron microscopy (TEM), photoluminescence and UV/Vis spectroscopies, and X-ray diffraction (XRD). Time-dependent TEM investigations revealed that time plays a vital role in this electrochemical transformation. This electrochemical transformation provides a facile method to obtain WS QDs from their bulk counterpart, which is expected to have a greater impact on the design and development of nanostructures derived from 2D materials.

No abstract

A single-step electrochemical disintegration of bulk WS2 led to a highly active WS2 QDs electrocatalyst for HER.