Chiroptical Properties of Semiconducting Nanoplatelets Functionalized by Tartrate Derivatives.

Inducing chirality in semiconductor nanoparticles is a recent trend motivated by the possible applications in circularly polarized light emission, spintronics, or stereoselective synthesis. However, the previous reports on CdSe nanoplatelets (NPLs) exclusively rely on cysteine or its derivatives as chiral ligands to induce optical activity. Here, we show a strong induction of chirality with derivatives of tartaric acid obtained by a single-step synthesis. The ligand exchange procedure in organic solvent was optimized for five-monolayer (5 ML) NPLs but can also be performed on 4, 3, and 2 ML. We show that the features of the CD spectra change with structural modification of the ligands and that these chiral ligands interact mainly with the first light-hole (lh1) band rather than the first heavy-hole (hh1) band, contrary to cysteine. This result suggests that chiroptical properties could be used to probe CdSe nanoplatelets' surface ligands.

An Amorphous Phase Precedes Crystallization: Unraveling the Colloidal Synthesis of Zirconium Oxide Nanocrystals.

One can nowadays readily generate monodisperse colloidal nanocrystals, but the underlying mechanism of nucleation and growth is still a matter of intense debate. Here, we combine X-ray pair distribution function (PDF) analysis, small-angle X-ray scattering (SAXS), nuclear magnetic resonance (NMR), and transmission electron microscopy (TEM) to investigate the nucleation and growth of zirconia nanocrystals from zirconium chloride and zirconium isopropoxide at 340 °C, in the presence of surfactant (tri-n-octylphosphine oxide). Through E1 elimination, precursor conversion leads to the formation of small amorphous particles (less than 2 nm in diameter). Over the course of the reaction, the total particle concentration decreases while the concentration of nanocrystals stays constant after a sudden increase (nucleation). Kinetic modeling suggests that amorphous particles nucleate into nanocrystals through a second order process and they are also the source of nanocrystal growth. There is no evidence for a soluble monomer. The nonclassical nucleation is related to a precursor decomposition rate that is an order of magnitude higher than the observed crystallization rate. Using different zirconium precursors (e.g., ZrBr4 or Zr(OtBu)4), we can tune the precursor decomposition rate and thus control the nanocrystal size. We expect these findings to help researchers in the further development of colloidal syntheses.

Curvature and self-assembly of semi-conducting nanoplatelets.

Semi-conducting nanoplatelets are two-dimensional nanoparticles whose thickness is in the nanometer range and controlled at the atomic level. They have come up as a new category of nanomaterial with promising optical properties due to the efficient confinement of the exciton in the thickness direction. In this perspective, we first describe the various conformations of these 2D nanoparticles which display a variety of bent and curved geometries and present experimental evidences linking their curvature to the ligand-induced surface stress. We then focus on the assembly of nanoplatelets into superlattices to harness the particularly efficient energy transfer between them, and discuss different approaches that allow for directional control and positioning in large scale assemblies. We emphasize on the fundamental aspects of the assembly at the colloidal scale in which ligand-induced forces and kinetic effects play a dominant role. Finally, we highlight the collective properties that can be studied when a fine control over the assembly of nanoplatelets is achieved.

Beyond the Concentration Limitation in the Synthesis of Nanobipyramids and Other Pentatwinned Gold Nanostructures.

Gold nanoparticles offer unique optoelectronic properties relevant for a wide range of processes and products, in biology and medicine (therapeutic agents, diagnostic, drug delivery), as well as in electronics, photovoltaics, and catalysis. So far, various synthesis methods proposed have led to rather limited concentration and purity of the colloidal suspensions, severely hindering their use. Here, we present a simple and versatile procedure for the synthesis of gold pentatwinned nanostructures, including nanobipyramids based on a seed-mediated growth process that overcomes the concentration limitations of current methods by 2 orders of magnitude. Moreover, our novel process offers quantitative yields while easily allowing a fine control of the particles' shape, size (with a high monodispersity), and plasmonic properties. Finally, we demonstrate that our method can be easily upscaled to produce large amounts of nanostructures, up to the gram scale, with minimal waste and postprocessing, thus facilitating their use for further applications and industrial developments.