Binary photoluminescent semiconductor nanocrystals (quantum
dots,
QDs) are one of the best studied fluorescent nanomaterials, and their
unique optoelectronic properties paved the road to many applications
in (bio)nanophotonics, optoelectronics, and photovoltaics. However,
concerns related to their toxic constituents like cadmium or lead
and the emerging interest in greener chemistry synthesis approaches
hamper their future applicability. Interesting alternatives for some
applications like biosensing or bioimaging are heavy-metal-free ternary
QDs like AgInS2 (AIS), CuInS2 (CIS), and quaternary
QDs such as AIS-ZnS (ZAIS). In this context, we explored the effect
of ligand denticity on the organic-to-aqueous phase transfer of oleylamine-stabilized
ZAIS QDs with the hydrophilic ligands mercaptopropionic acid (MPA),
dihydrolipoic acid (DHLA), and 3-mercapto-2,2-bis(mercaptomethyl)propanoic
acid (3MPA), bearing mono-, bi-, and trialkyl thiol groups. Spectroscopic
studies of the resulting water-dispersible ZAIS QDs revealed a considerable
influence of ligand denticity and ligand-to-QD ratio on the spectral
position and width (FWHM; full width at half-maximum) of the photoluminescence
(PL) bands, the PL quantum yields (PL QY), and the PL decay kinetics.
Thiol capping and phase transfer resulted in a loss in PL by at least
a factor of 2. The ligand-induced PL quenching observed particularly
for ligands bearing two or three thiol groups was attributed to the
facilitated formation of surface-bound disulfides. The best colloidal
stability under high dilution conditions was observed for 3MPA.