Inorganic
two-dimensional semiconductor nanostructures intrigue
the scientific community because of their tunable and sparse electronic
states and their high conductivity. The current work deals with colloidal
nanoplatelets (NPLs) based on In2S3 compound,
focusing on the growth mechanism that leads to the formation of two
different phases, trigonal γ-In2S3 and
defect spinel β-In2S3, both stabilized
at room temperature and characterized by ordered metal voids. In particular,
we substantiate the experimental factors (e.g., temperature, reaction
duration, and surface ligands) that control the growth progress. The
results indicated the formation of hexagonal NPLs of the γ-phase
at an elevated temperature and dodecagon NPLs of the γ-phase
at a lower temperature. A long-reaction duration time transformed
the hexagons/dodecagons into truncated triangular shapes. Furthermore,
the analysis of thermodynamic and kinetic factors indicated a phase
transformation from the γ-phase to the β-phase. All phases
were produced by a new colloidal procedure based on a single precursor.
The structures created were verified by X-ray diffraction, high-resolution
transmission electron microscopy analyses, and Raman measurements.
Elementary optical properties were identified by absorption and emission
measurements. The nanoplatelets discussed offer low toxicity and optical
activity in the UV and visible spectral regimes and an option for
electrical or magnetic doping, enabled by the existing voids.