Reaction chemistry/nanocrystal property relations in the hot injection synthesis, the role of the solute solubility.

Various literature studies show that increasing the concentration of free acid in the hot injection synthesis of colloidal nanocrystals raises the diameter of the resulting nanocrystals. We analyze this reaction chemistry/nanocrystal property relation by combining reaction simulations with an experimental study on a particular CdSe nanocrystal synthesis. We find that increasing the free acid concentration has the same effect on a real synthesis as raising the solute solubility in the simulations.

Broadband and picosecond intraband absorption in lead-based colloidal quantum dots.

Using femtosecond transient absorption spectroscopy, we demonstrate that lead chalcogenide nanocrystals show considerable photoinduced absorption (PA) in a broad wavelength range just below the band gap. The time-dependent decay of the PA signal correlates with the recovery of the band gap absorption, indicating that the same carriers are involved. On this basis, we assign this PA signal to intraband absorption, that is, the excitation of photogenerated carriers from the bottom of the conduction band or the top of the valence band to higher energy levels in the conduction and valence band continuum.

Tuning the postfocused size of colloidal nanocrystals by the reaction rate: from theory to application.

We show that adjusting the reaction rate in a hot injection synthesis is a viable strategy to tune the diameter of colloidal nanocrystals at the end of the size distribution focusing, i.e., the postfocused diameter.

Size-tunable, bright, and stable PbS quantum dots: a surface chemistry study.

PbS Qdots are synthesized using PbCl2 and elemental sulfur as precursors. The available size range is significantly expanded using tri-n-octylphosphine (TOP), enabling the synthesis of monodisperse suspensions of Qdots with a mean size varying between 3 and 10 nm. The ligand composition and dynamics are investigated with nuclear magnetic resonance (NMR) spectroscopy.

The different nature of band edge absorption and emission in colloidal PbSe/CdSe core/shell quantum dots.

We present a quantitative analysis of the absorption and luminescence of colloidal PbSe/CdSe core/shell quantum dots (QDs). In absorption, both the energy and the oscillator strength of the first exciton transition coincide with that of plain PbSe QDs. In contrast, luminescence lifetime measurements indicate that the oscillator strength of the emitting transition is reduced by at least a factor of 4 compared to PbSe core QDs.