Quantum-confined CdTe nanoplatelets (NPL) are synthesized in colloidal solutions. The formation, growth, and transformation of 2D NPLs are monitored using UV-visible absorption PL spectroscopy and transmission electron microscopy. The luminescence intensity of NPL dependences on the temperature and injection of precursors is shown. It is found that the luminescence spectra shift to the long-wavelength region with increasing temperature due to an increase in the thickness of the NPL. The dependence of the band gap on the thickness of the NPL is shown. The band gap is determined by the thickness and number of layers. The dependence of the concentration of precursors in the reaction mass and the kinetics of NPL growth are shown. The excitation of defect states luminescence depends on the coordinating oleic ligand. The crystal structure of the CdTe NPL was analyzed via the electron diffraction pattern (ED), which allows a comparative conclusion about the crystal structure of the obtained NPL samples.

Colloidal quasi-two-dimensional cadmium chalcogenide nanoplatelets have attracted considerable interest due to their narrow excitonic emission and absorption bands, making them promising candidates for advanced optical applications. In this study, the synthesis of quasi-two-dimensional CdSe NPLs with a thickness of 3.5 monolayers was investigated to understand the effects of synthesis temperature on their stoichiometry, morphology, and optical properties. The NPLs were synthesized using a colloidal method with temperatures ranging from 170 °C to 210 °C and optimized precursor ratios. Total reflection X-ray fluorescence (TXRF) analysis was employed to determine stoichiometry, while high-resolution transmission electron microscopy (HRTEM) and UV-Vis spectroscopy and photoluminescence spectroscopy were used to analyze the structural and optical characteristics. The results showed a strong correlation between increasing synthesis temperature and the enlargement of nanoscroll diameters, indicating dynamic growth. The best results in terms of uniformity, stoichiometry, and optical properties were achieved at a growth temperature of 200 °C. At this temperature, no additional optical bands associated with secondary populations or hetero-confinement were observed, indicating the high purity of the sample. Samples synthesized at lower temperatures exhibited deviations in stoichiometry and optical performance, suggesting the presence of residual organic compounds.

Colloidal cadmium telluride (CdTe) nanoplatelets (NPLs) are promising materials for optoelectronic applications, such as photovoltaics and light-emitting diodes, due to their unique optical and electronic properties. However, controlling their growth, thickness, and stoichiometry remains challenging. This study explores the effect of synthesis temperature on the structural, optical, and stoichiometric properties of CdTe NPLs. CdTe NPLs were synthesized at temperatures of 170 °C, 180 °C, 190 °C, and 200 °C using colloidal methods. The resulting NPLs were characterized by UV–Vis absorption spectroscopy, photoluminescence (PL) spectroscopy, transmission electron microscopy (TEM), and total reflection X-ray fluorescence (TXRF) to assess their morphology, structure, and elemental composition. The results showed that the synthesis temperature significantly affected the NPL’s morphology and stoichiometry. Optimal stoichiometry was achieved at 180 °C and 190 °C, with the crystal structure transitioning from zinc blende at lower temperatures to wurtzite at higher temperatures. Optical properties, including luminescence intensity and emission peaks, also varied with temperature. The synthesis temperature is an important parameter in controlling the structural and optical properties of CdTe NPLs. The optimal conditions for obtaining NPLs with the best characteristics were identified at 190 °C, presenting important findings for further optimization of CdTe NPL synthesis for optoelectronic applications.

Absorption spectra are widely used in laboratory practice to measure the content of a great variety of colloidal semiconductor nanocrystals. In the case of atomically thin nanoplatelets, only CdSe has been studied enough to allow such quantification, while CdTe nanoplatelets—a promising material for photodetection—are understudied in this regard. In this work, a powerful combination of total XRF spectroscopy, absorption spectroscopy and profilometry was employed for thin films to extract the absorption coefficient values. The morphology and surface composition of nanoplatelets were studied with TEM and IR spectroscopy. The molar absorption coefficient of oleate-terminated CdTe nanoplatelets at the first optical transition was measured at about 5 × 10⁴ L·mol⁻¹·cm⁻¹ (per mole of Te), which is among the highest values for AIIBVI nanomaterials. The exchange of stabilizer with hexadecanethiol induced an approximately 5-fold decrease in the volume fraction of semiconductor material in thin films and a 5-fold decrease in absorbance. The latter effect is linked to the formation of a quasi-type II heterojunction between CdTe cores and effectively half of a monolayer shell of CdS. The density effect is explained by the diminished capacity of nanoscrolls for close packing. The combination of XRF and profilometry is proposed as a technique for fast nanomorphology evaluation.

CdTe colloidal nanoplatelets (NPLs) are promising two-dimensional quantum emitters, but their surface chemistry has been less studied compared to CdSe NPLs. Understanding and controlling surface properties are critical for their application. In this work, we investigate the conditions under which CdTe NPLs remain stable during post-synthetic ligand exchange in mild organic environments, which is a key step for their further use. During the initial stage of the work, the effect of the stoichiometric ratio of precursors on the optical characteristics and chemical composition of CdTe NPLs obtained at a temperature of 170 °C was analysed. The concentrations of Cd and Te varied within ±50% with respect to our standard version. The results obtained by TXRF demonstrated the formation of compositions with a moderate excess of cadmium (the Cd/Te ratio varied from 1.03 to 1.19). These conclusions are consistent with the concept of Cd-terminated surfaces stabilized by carboxylate ligands. Three standard ligand exchange strategies successfully applied to CdSe nanocrystals (carboxylate → CdCl₂, → Zn(DDTC)₂ and → hexadecanethiol) were tested on CdTe nanocrystals. Contrary to expectations, treatment of CdTe with CdCl₂ or Zn(DDTC)₂ solutions did not result in a measurable shift in exciton transitions and, moreover, caused degradation of the colloidal dispersion. Our studies have identified a range of conditions under which CdTe NPLs retain their integrity during ligand exchange. While some elements of the CdSe-developed protocols can be transferred to CdTe, their applicability is limited by a narrow processing window: beyond a certain treatment time, CdTe nanoplatelets progressively lose optical stability