Passivation, phase, and morphology control of CdS nanocrystals probed using fluorinated aromatic amines and solid-state NMR spectroscopy.

Nanocrystals are widely explored for a range of medical, imaging, sensing, and energy conversion applications. CdS nanocrystals have been reported as excellent photocatalysts, with thin film CdS also highly important in photovoltaic devices. To optimise properties of nanocrystals, control over phase, facet, and morphology are vital. Here, CdS nanocrystals were synthesised by the solvothermal decomposition of a Cd xanthate single source precursor. To attempt to control CdS nanocrystal surfaces and morphology, the solvent used in the nanocrystal synthesis was altered from pure trioctylphosphine oxide (TOPO) to a mixed TOPO : fluorinated aromatic amine (3-fluorobenzyl amine (3-FlBzAm) or 3-fluoroaniline (3-FlAn)), where F provides a sensitive NMR-active surface probe. Powder X-ray diffraction found that the CdS nanocrystals synthesised from TOPO : 3-FlAn solvent mixtures were predominantly cubic whilst the TOPO : 3-FlBzAm synthesised nanocrystals were predominantly hexagonal. Raman spectroscopy identified hexagonal CdS in all samples. Solid-state NMR of Cd, F, C, and H was employed to investigate the local Cd environments, surface ligands, and ligand interactions. This showed there was a mixture of CdS phases present in all samples and that surfaces were capped with TOPO : fluorinated aromatic amine mixtures, but also that there was a stronger binding affinity of 3-FlBzAm compared with 3-FlAn on the CdS surface, which likely impacts growth mechanisms. This work highlights that fluorinated aromatic amines can be used to probe NC surfaces and also control NC properties through their influence during NC growth.