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Correlation among particles in finite quantum systems leads to complex behaviour and novel states of matter. One remarkable example is predicted to occur in a semiconductor quantum dot (QD) where at vanishing density the Coulomb correlation among electrons rigidly fixes their relative position as that of the nuclei in a molecule. In this limit, the neutral few-body excitations are roto-vibrations, which have either rigid-rotor or relative-motion character. In the weak-correlation regime, on the contrary, the Coriolis force mixes rotational and vibrational motions. Here we report evidence of roto-vibrational modes of an electron molecular state at densities for which electron localization is not yet fully achieved. We probe these collective modes by inelastic light scattering in QDs containing four electrons. Spectra of low-lying excitations associated to changes of the relative-motion wave function -the analogues of the vibration modes of a conventional molecule- do not depend on the rotational state represented by the total angular momentum. Theoretical simulations via the configuration-interaction (CI) method are in agreement with the observed roto-vibrational modes and indicate that such molecular excitations develop at the onset of short-range correlation.Comment: PDF file only; 24 pages, 7 figures, 2 table. Supplementary Information include

We demonstrate the in-plane emission of highly-polarized single photons from an InAs quantum dot embedded into a photonic crystal waveguide. The spontaneous emission rates are Purcell-enhanced by the coupling of the quantum dot to a slowlight mode of the waveguide. Photon-correlation measurements confirm the sub-Poissonian statistics of the in-plane emission. Under optical pulse excitation, single photon emission rates of up to 19 MHz into the guided mode are demonstrated, which corresponds to a device efficiency of 24%. These results herald the monolithic integration of sources in photonic quantum circuits.

Blinking and spectral diffusion are hallmarks of nanoscale light emitters and a challenge for creating stable fluorescent biomarkers or efficient nonclassical light sources. Here, we demonstrate suppression of blinking and spectral diffusion of individual single-wall carbon nanotubes by manipulation of their dielectric environment, resulting in 5-fold enhanced light emission. In addition, it was found that the characteristic slopes of the blinking power laws are largely independent of the dielectric environment in the limit of a large number of switching events. In contrast, the on/off ratio determined from statistical occurrence analysis is found to be improved by 3 orders of magnitude toward the on state, making the on/off ratio an important measure for charge transfer from/into the local dielectric environment of a quantum emitter. Furthermore, our approach is compatible with integration into cavities, in contrast to previous demonstrations of spectral diffusion suppression achieved in free-standing single-wall carbon nanotubes. This opens up possibilities to couple the exciton emission of nonblinking carbon nanotubes to cavity modes to further benefit by the Purcell effect and to enhance the light extraction efficiency, in order to ultimately demonstrate efficient photonic devices.