We report the realization of a mechanically flexible microcavity laser emitting at 657 nm using spin coating. These optically pumped vertical cavity surface emitting lasers use InGaP colloidal quantum dots as the active medium and alternating polymer layers of different refractive indices as the Bragg mirrors. Results of photoluminescence measurements indicating enhancement in spontaneous emission are presented. We also demonstrate the possibility of peeling the device off the substrate yielding a flexible structure that can conform to any shape and whose emission spectra can be mechanically tuned. This new class of hybrid lasers combines advantages of organic and inorganic materials.

The tunability of electronic and optical properties of semiconductor nanocrystal quantum dots (QDs) has been an important subject in nanotechnology. While control of the emission property of QDs in wavelength has been studied extensively, control of the emission lifetime of QDs has not been explored in depth. In this report, ZnO-CdS core–shell QDs were synthesized in a two-step process, in which we initially synthesized ZnO core particles, and then stepwise slow growth of CdS shells followed. The coating of a CdS shell on a ZnO core increased the exciton lifetime more than 100 times that of the core ZnO QD, and the lifetime was further extended as the thickness of shell increased. This long electron–hole recombination lifetime is due to a unique staggered band alignment between the ZnO core and CdS shell, so-called type II band alignment, where the carrier excitation holes and electrons are spatially separated at the core and shell, and the exciton lifetime becomes extremely sensitive to the thickness of the shell. Here, we demonstrated that the emission lifetime becomes controllable with the thickness of the shell in ZnO-CdS core–shell QDs. The longer excitonic lifetime of type II QDs could be beneficial in fluorescence-based sensors, medical imaging, solar cells photovoltaics, and lasers.

Conventional Förster resonance energy transfer (FRET) processes involving a pair of fluorophore and organic quencher are restricted to an upper distance limit of ~10 nm. The application of a metal nanoparticle as a quencher can overcome the distance barrier of the traditional FRET technique. However, no standard distance dependence of this resonance energy transfer (RET) process has been firmly established. We have investigated the nonradiative energy transfer process between an organic donor (fluorescein) and gold nanoparticle quencher connected by double stranded (ds) DNA. The quenching efficiency of the gold nanoparticle as a function of distance between the donor and acceptor was determined by time-resolved lifetime analyses of the donor. Our results showed a 1/d4 distance dependence for the RET process for longer distances (>10 nm) and 1/d6 distance dependence for shorter distances (<10 nm). Our results clearly indicate the applicability of metal nanoparticle based quenchers for studying systems that exceed the 10 nm FRET barrier.