Synthesis
protocols for colloidal nanocrystals (NCs) with narrow
size and shape distributions are of particular interest for the successful
implementation of these nanocrystals into devices. Moreover, the preparation
of NCs with well-defined crystal phases is of key importance. In this
work, we show that Sn(IV)-thiolate complexes formed in situ strongly
influence the nucleation and growth rates of colloidal Cu2–xS polyhedral NCs, thereby dictating their final size,
shape, and crystal structure. This allowed us to successfully synthesize
hexagonal bifrustums and hexagonal bipyramid NCs with low-chalcocite
crystal structure, and hexagonal nanoplatelets with various thicknesses
and aspect ratios with the djurleite crystal structure, by solely
varying the concentration of Sn(IV)-additives (namely, SnBr4) in the reaction medium. Solution and solid-state 119Sn NMR measurements show that SnBr4 is converted in situ
to Sn(IV)–thiolate complexes, which increase the Cu2–xS nucleation barrier without affecting the precursor
conversion rates. This influences both the nucleation and growth rates
in a concentration-dependent fashion and leads to a better separation
between nucleation and growth. Our approach of tuning the nucleation
and growth rates with in situ-generated Sn–thiolate complexes
might have a more general impact due to the availability of various
metal–thiolate complexes, possibly resulting in polyhedral
NCs of a wide variety of metal–sulfide compositions.