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Abstract NaCl has widely been used as a seeding promoter for chemical vapor deposition of large-scale 2D transition metal dichalcogenides. In this work, we report a study of the influence of NaCl on the growth and optical properties of layered CVD-grown WS₂using steady-state and time-resolved Kerr rotation measurements at room temperature. Strong photoluminescence (PL) signals from single flakes grown with a low NaCl content indicates direct band-gap emission, whereas flakes grown with higher amounts of NaCl exhibit red-shifted, weaker PL. Raman measurements from single flakes also indicate that WS₂grown with higher NaCl amounts result in multilayered structures, while lower NaCl quantities yield monolayer WS₂. Ultrafast carrier decay measurements from single flakes also indicate a NaCl-dependent on the valley exchange interaction component (<10 ps) and slower decay components (>50 ps), attributed to a combination of phenomena, such as the band gap transitioning from direct to indirect and defect-related localized states. Our study provides insight into the influence of seeding promoters in layered CVD-grown WS₂in particular and 2D transition metal dichalcogenides in general. 

Tellurium is a heavy chemical element exhibiting chirality, anisotropy, and strong spin-orbit coupling; conse quently, displaying a huge potential in quantum hardware technologies. In this article, tellurium quantum dots, with sizes around 19 ± 3 nm and energy bandgap around 2.4 eV, were successfully synthesized by pulsed laser ablation in liquids (PLAL). The synthesis was performed by using a nanosecond Nd:YAG laser emitting at 1064 nm and pulsing the laser beam at 1 kHz. Toluene (C6H5CH3) was used as a solvent to avoid oxidation of the dots. Non-polarized and polarized Raman spectroscopy as well as X-Ray diffraction were performed on the dots to study their quantum confinement and anisotropy. Finally, strongly confined tellurium quantum dots were obtained; and, their properties underline their potential as quantum light sources. 

Bismuth oxide is an important bismuth compound having applications in electronics, photo-catalysis and medicine. At the nanoscale, bismuth oxide experiences a variety of new physico-chemical properties because of its increased surface to volume ratio leading to potentially new applications. In this manuscript, we report for the very first time the synthesis of bismuth oxide (Bi 2 O 3 ) nano-flakes by pulsed laser ablation in liquids without any external assistance (no acoustic, electric field, or magnetic field). The synthesis was performed by irradiating, pure bismuth needles immerged in de-ionized water, at very high fluence ∼160 J cm −2 in order to be highly selective and only promote the growth of two-dimensional structures. The x - and y -dimensions of the flakes were around 1 μm in size while their thickness was 47.0 ± 12.7 nm as confirmed by AFM analysis. The flakes were confirmed to be α- and γ-Bi 2 O 3 by SAED and Raman spectroscopy. By using this mixture of flakes, we demonstrated that the nanostructures can be used as antimicrobial agents, achieving a complete inhibition of Gram positive (MSRA) and Gram negative bacteria (MDR-EC) at low concentration, ∼50 ppm.