Dedicated to Professor Jozef T. Devreese on the occasion of his 65th birthday PACS 73.21.La, 78.20.Hp, 78.35.+c, 78.67.HcThe exciton-LO-phonon interaction in self-organized quantum dots is investigated emphasizing the impact of realistic structural properties. The possibility to engineer the local charge density via the shape and composition profile of such strained quantum dots provides an unique opportunity to optimize the electronic and optical properties of a semiconductor nanostructure. Size-selective luminescence, resonant Raman scattering, and time-resolved luminescence experiments provide insight into the exciton-LO-phonon and exciton-photon couplings in self-organized quantum dots. The impact of the structural details is analyzed based on eight-band k Á p model calculations.1 Introduction The interest in semiconductor quantum dots (QD's) results foremost from the modification of the electronic eigenstate spectrum [1]. The three-dimensional confinement leads to a discrete density of states drastically narrowing the thermal carrier distribution and limiting interaction processes [2]. The mesoscopic nature of QD's, which consist out of thousands of atoms, allows for a large diversity of structural realizations. The non-trivial relation between structural and electronic properties of QD's carries the potential to engineer the electronic/optical properties. In recent years it became clear that the detailed understanding of localized excitations in QD's requires to account for the interaction with lattice vibrations, i.e. phonons. The coupling to phonons determines, e.g., the line shape of transitions and the carrier dynamics. A detailed understanding of the effects of localizing a carrier/exciton in a QD on the interaction with phonons is essential, in particular for device applications.The observation of phonon-assisted transitions in optical spectra, i.e. phonon-assisted generation and recombination of excitons, or resonant Raman scattering provide information on the interaction with phonons. Experimentally, the main problem is the generally large inhomogeneous broadening of QD ensembles, typically exceeding the relevant phonon energies. Employing size-selective spectroscopy pronounced LO-phonon sidebands have been identified for almost spherical, unstrained II-VI QD's [3][4][5][6][7]. In the adiabatic approximation, the coupling strength is usually represented by the dimensionless Huang-Rhys factor [8] and can be directly estimated from the intensity ratios of different order phonon processes. Values of the order of unity have been reported for the polar exciton-LO-phonon coupling. The Fraehlich coupling of the exciton to a LO-phonon is proportional to the local charge