Although multiphoton-pumped lasing from a solution of chromophores is important in the emerging fields of nonlinear optofluidics and bio-photonics, conventionally used organic dyes are often rendered unsuitable because of relatively small multiphoton absorption cross-sections and low photostability. Here, we demonstrate highly photostable, ultralow-threshold multiphoton-pumped biexcitonic lasing from a solution of colloidal CdSe/CdS nanoplatelets within a cuvette-based Fabry–Pérot optical resonator. We find that colloidal nanoplatelets surprisingly exhibit an optimal lateral size that minimizes lasing threshold. These nanoplatelets possess very large gain cross-sections of 7.3 × 10−14 cm2 and ultralow lasing thresholds of 1.2 and 4.3 mJ cm−2 under two-photon (λexc=800 nm) and three-photon (λexc=1.3 μm) excitation, respectively. The highly polarized emission from the nanoplatelet laser shows no significant photodegradation over 107 laser shots. These findings constitute a more comprehensive understanding of the utility of colloidal semiconductor nanoparticles as the gain medium in high-performance frequency-upconversion liquid lasers.

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We describe a surfactant-driven method to synthesize highly monodisperse CdSe-seeded CdS tetrapods with differing arm lengths and diameters in order to examine their effects on self-assembly. We exploited the phenomena of weak-and strong-binding capping groups to tune the arm length and diameter with uniform shape and achieved >95% yield. Afterward, we utilize these particles to overcome some of the key problems in the assembly of anisotropic shaped particles. Intriguingly, we found that tetrapods with certain arm lengths pack like fishbone chains, which was greatly dependent on particle shape and size. These ordered assembly phenomena were understood with the assistance of computer simulations, which strongly support our experimental observations. Importantly, this work presents a synthetic route toward shape tuning in CdSe-seeded CdS tetrapod structures, which has great influence on their self-assembly behavior at the solution/substrate interface.

Core/shell tetrapods synthesized from CdSe and CdTe exhibit a type II band offset that induces separation of charge upon photoexcitation and localizes carriers to different regions of the tetrahedral geometry. CdSe/CdTe nanocrystals immobilized on oleylamine‐functionalized reduced graphene oxide (rGO) sheets can be homogeneously mixed with an organic dye (PCDTBT) to form donor–acceptor dispersed heterojunctions and exhibit a high power conversion efficiency of ∼3.3% in solar cell devices. The near‐IR light absorbing type II nanocrystals complement the absorption spectrum of the visible light‐absorbing organics. The high efficiency is attributed to the amine‐functionalized rGO sheets, which allow intimate contact with the nanocrystals and efficient dispersal in the organic matrix, contributing to highly efficient charge separation and transfer at the nanocrystal, rGO, and polymer interfaces.

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Wet-chemically synthesized 2D transition metal sulfides (TMS) are promising materials for catalysis, batteries and optoelectronics, however a firm understanding on the chemical conditions which result in selective lateral growth has been lacking. In this work we demonstrate that Ni9S8, which is a less common nonstoichiometric form of nickel sulfide, can exhibit two-dimensional growth when halide ions are present in the reaction. We show that the introduction of halide ions reduced the rate of formation of the nickel thiolate precursor, thereby inhibiting nucleation events and slowing growth kinetics such that plate-like formation was favored. Structural characterization of the Ni9S8 nanoplates produced revealed that they were single-crystal with lateral dimensions in the range of ∼100–1000 nm and thicknesses as low as ∼4 nm (about 3 unit cells). Varying the concentration of halide ions present in the reaction allowed for the shape of the nanostructures to be continuously tuned from particle- to plate-like, thus offering a facile route to controlling their morphology. The synthetic methodology introduced was successfully extended to Cu2S despite its different growth mechanism into ultrathin plates. These findings collectively suggest the importance of halide mediated slow growth kinetics in the formation of nanoplates and may be relevant to a wide variety of TMS.

We synthesized colloidal InP/ZnS seeded CdS tetrapods by harnessing the structural stability of the InP/ZnS seed nanocrystals at the high reaction temperatures needed to grow the CdS arms. Because of an unexpected Type II band alignment at the interface of the InP/ZnS core and CdS arms that enhanced the occurrence of radiative excitonic recombination in CdS, these tetrapods were found to be capable of exhibiting highly efficient multiexcitonic dual wavelength emission of equal intensity at spectrally distinct wavelengths of ∼485 and ∼675 nm. Additionally, the Type II InP/ZnS seeded CdS tetrapods displayed a wider range of pump-dependent emission color-tunability (from red to white to blue) within the context of a CIE 1931 chromaticity diagram and possessed higher photostability due to suppressed multiexcitonic Auger recombination when compared to conventional Type I CdSe seeded CdS tetrapods. By employing time-resolved spectroscopy measurements, we were able to attribute the wide emission color-tunability to the large valence band offset between InP and CdS. This work highlights the importance of band alignment in the synthetic design of semiconductor nanoheterostructures, which can exhibit color-tunable multiwavelength emission with high efficiency and photostability.

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