AbstractColloidal semiconductor nanocrystals or quantum dots are an important building block in bottom-up nanotechnology. They consist of an inorganic, crystalline core surrounded by a monolayer of organic ligands. As these ligands can be modified or exchanged for others, they provide a convenient way to give the quantum dots functionality. Here, we show that solution NMR techniques, including diffusion pulsed field gradient spectroscopy, is a very useful tool to investigate the ligands of colloidal nanocrystals. This is demonstrated using InP quantum dots with trioctylphospine oxide ligands as an example. Combining 1H-13C HSQC spectroscopy with pulsed field gradient diffusion NMR, an unequivocal identification of the resonances of the bound ligands is possible. This leads to the determination of the diffusion coefficient of the nanocrystals in solution and allows to verify capping exchange procedures. By calibrating the surface area of the NMR resonances using a solute of known concentration, the density of ligands at the nanocrystal surface can be quantified. We could demonstrate that a dynamic equilibrium exists between bound and free ligands. Analysis of the corresponding adsorption isotherm - determined using 1H NMR - leads to an estimation of the free energy of adsorption and the free energy of ligand-ligand interaction at the nanocrystals surface. Similar investigations are in progress on capped PbSe and ZnO2 nanoparticles. Preliminary results strongly support the generic nature of the approach described for the case of TOPO capped InP nanocrystals.
The adsorption characteristics and porous structure of bentonite adsorbents, determined from the adsorption isotherms of benzene vapor
