We report on the temperature dependence of the photoluminescence (PL) spectrum and of the PL relaxation dynamics for colloidal $\mathrm{Cd}\mathrm{Se}∕\mathrm{Zn}\mathrm{S}$ core/shell quantum dots (QDs) embedded in an inert polystyrene matrix. We demonstrate that the confinement energy in the QDs is independent of the temperature. The coupling with both acoustic and optical phonons is also studied. Quantum confinement results in a strong increase of the exciton–acoustic-phonon coupling constant, up to $71\mu \mathrm{eV}∕\mathrm{K}$, and in a reduced exciton–longitudinal-optical (LO)-phonon coupling constant, down to $21\mathrm{meV}$, with respect to bulk CdSe. In addition, we demonstrate that the main nonradiative process that limits the quantum efficiency of the QD at room temperature is the thermal escape from the dot assisted by scattering with four LO phonons. Thermally activated trapping in surface states is also observed at low temperature, with an activation energy of about $15\mathrm{meV}$.

We have investigated the effects of the built-in electric field in ${\mathrm{G}\mathrm{a}\mathrm{N}/\mathrm{A}\mathrm{l}}_{0.15}{\mathrm{Ga}}_{0.85}\mathrm{N}$ quantum wells by photoluminescence spectroscopy. The fundamental electron heavy-hole transition redshifts well below the GaN bulk gap for well widths larger than 3 nm for the specific quantum wells investigated and exhibits a concomitant reduction of the intensity with increasing well thickness. The experimental data are quantitatively explained by means of a self-consistent tight-binding model that includes screening (either dielectric or by free-carriers), piezoelectric field and spontaneous polarization field. The impact of the built-in field on the exciton stability is discussed in detail. We demonstrate that the exciton binding energy is substantially reduced by the built-in field, well below the values expected from the quantum size effect in the flat band condition.

We have studied the interactions in the solid phase between a blue-light-emitting organic conjugated polymer {poly[(9,9-dihexylfluorenyl-2,7-diyl)-alt-co-(9,ethyl-3,6-carbazole)]} and colloidal $\mathrm{CdSe}∕\mathrm{ZnS}$ core shell quantum dots. We demonstrate by time resolved photoluminescence measurements that efficient Förster energy transfer takes place from the polymer acting as the donor and the $\mathrm{CdSe}∕\mathrm{ZnS}$ dots, acting as the acceptors. A Förster radius of about $80\pm 15\mathrm{\AA }$ is extracted from the analysis of the relaxation dynamics based on the solution of the donor-acceptor coupled rate equations. This value is in good agreement with the value extracted from the steady state spectra and indicates that efficient energy tranfer from a polymeric host to a nanocrystal guest can occur. Our results are relevant to the application of hybrid organic/inorganic systems to light-emitting devices.