Using the immersion lensing technique, the resolution of a conventional spherical lens can be improved by a factor of 1/n over its value in air (n, the refractive index of the immersion medium). Depending on the relative position between an object and a lens, either a real or a virtual image is formed. Here we report a new physical phenomenon experimentally observed in the microscale lens imaging. We find that when a microscale spherical lens is semi-immersed in a medium, the resolution of the lens is improved as it can intercept more fine details of the object. However, the microscale lens has two image channels for the fine and coarse details and two images corresponding to the two components can be formed simultaneously. Our findings will advance the understanding of the super-resolution imaging mechanisms in microscale lenses.

Colloidal semiconductor quantum dots (QDs) have recently attracted great attention in electric field sensing via the quantum-confined Stark effect (QCSE), but they suffer from the random local electric field around the charged QDs through the Auger process or defect traps. Here, QCSE in the ensemble of phase-pure wurtzite CdSe/CdS QDs was studied by applying a uniform external electric field. We observed clear field-dependent photoluminescence (PL) and absorption characteristics in thick-shell CdSe/CdS QDs with 11 CdS monolayers (11 MLs) including a pronounced spectral redshift in PL of ∼2.3 nm and absorption of ∼2.1 nm. The time-dependent PL intensity traces implied that the thick-shell QDs were conducive to realize the Stark shift in QD ensembles due to the effective suppression of the main sources of the local field. These findings were in stark contrast to those of moderate-shell (5 MLs) and ultrathick-shell (15 MLs) CdSe/CdS QDs. The measurement value of exciton polarizability was smaller than the theoretical value, which may be influenced by very few exciton traps. Moreover, the amplified stimulated emission also exhibited obvious optical modulations under the electric field with decreased emission intensity and an increased ultrafast lifetime. Finally, the temporal evolution of the multiexciton process in thick-shell CdSe/CdS QDs indicated that the multiexciton state induced a higher energy state near the band edge, which may weaken the QCSE of a single exciton. Therefore, it was demonstrated that efficient field control over the optical properties of these nanomaterials is feasible and this can open up potential applications in field-controlled electro-optic modulators.

In this report, we mainly discussed the influence of surface/interfacial defects on the exciton recombination in CdZnSeS/ZnS QDs with different shell thicknesses by spectroelectrochemical and ultraviolet irradiation experiments.

When closely packed into a high-density film, semiconductor nanocrystals (NCs) can interact with each other to yield collective optical behaviours, which are normally difficult to characterize due to the ensemble average effect. Here we synthesized semiconductor NC clusters and performed single-particle spectroscopic measurements to probe the electronic couplings of several giant CdSe/CdS NCs contained in one cluster with nanometer-scale separations. Such a single cluster exhibits multiple emission peaks at the cryogenic temperature with nearly identical photoluminescence decay dynamics, suggesting that the Förster-type energy transfer does not occur among the composing NCs. Surprisingly, strong photon antibunching is still observed from a single cluster, which can be attributed to the Auger annihilation of photo-excited excitons from different NCs. The isolation of several nearby NCs interacting with the above novel mechanism has marked a solid progress towards a full understanding and an efficient control of the operation parameters in NC-based optoelectronic devices.

Colloidal CdSe quantum dots (QDs), whose surface traps are controlled with the purification process, are measured with a Z-scan technique using an 80 femtosecond pulse duration laser source. Their two-photon absorption coefficient and refractive index are decreased more than one order of magnitude with the increase of the density of surface traps, indicating that the surface states are involved in the two-photon process.