Colloidal semiconductor quantum dots are fluorescent nanocrystals exhibiting exceptional optical properties, but their emission intensity strongly depends on their charging state and local environment. This leads to blinking at the single-particle level or even complete fluorescence quenching, and limits the applications of quantum dots as fluorescent particles. Here, we show that a single quantum dot encapsulated in a silica shell coated with a continuous gold nanoshell provides a system with a stable and Poissonian emission at room temperature that is preserved regardless of drastic changes in the local environment. This novel hybrid quantum dot/silica/gold structure behaves as a plasmonic resonator with a strong Purcell factor, in very good agreement with simulations. The gold nanoshell also acts as a shield that protects the quantum dot fluorescence and enhances its resistance to high-power photoexcitation or high-energy electron beams. This plasmonic fluorescent resonator opens the way to a new family of plasmonic nanoemitters with robust optical properties.
We study the synthesis of indium phosphide quantum dots using InCl 3 , tris(dimethylamino)phosphine (P-(NMe 2 ) 3 ), and oleylamine. We optimized the reaction conditions to reach high chemical yield (∼70%) and size control of the quantum dots with absorption maxima over all the visible range. Kinetic studies of the formation of the quantum dots show that, under certain conditions, the growth of nanoparticles seems to approach a LaMer type growth. We have used 31 P NMR, mass spectroscopy, and DFT calculations to decipher the reaction mechanisms of InP formation at the molecular level. The mechanistic investigation is in good agreement with the conclusions drawn from the optimization of the synthetic conditions.
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We study in details the synthesis of CdTe nanoplatelets. Three populations of nanoplatelets with a thickness defined with atomic precision are obtained. We show that CdTe nanoplatelets can be extended laterally to obtain nanosheets with lateral dimensions in the micron range. We present the study of the reaction conditions for the formation of CdTe nanoplatelets and for their lateral extensions. The reaction products are analyzed with optical spectroscopy, transmission electron microscopy and small angle X-ray scattering. We investigate the electro-optical properties of films formed with CdTe nanoplatelets, and we show that their current photo-response is better than the one of comparable films formed with CdTe spherical nanocrystals.
To use water as the source of electrons for proton or CO reduction within electrocatalytic devices, catalysts are required for facilitating the proton-coupled multi-electron oxygen evolution reaction (OER, 2 H O→O +4 H +4 e ). These catalysts, ideally based on cheap and earth abundant metals, have to display high activity at low overpotential and good stability and selectivity. While numerous examples of Co, Mn, and Ni catalysts were recently reported for water oxidation, only few examples were reported using copper, despite promising efficiencies. A rationally designed nanostructured copper/copper oxide electrocatalyst for OER is presented. This material derives from conductive copper foam passivated by a copper oxide layer and further nanostructured by electrodeposition of CuO nanoparticles. The generated electrodes are highly efficient for catalyzing selective water oxidation to dioxygen with an overpotential of 290 mV at 10 mA cm in 1 m NaOH solution.
An amorphous cobalt–cobalt oxide/cobalt selenide composite film has been fabricated directly on a 3D macro-porous Ni foam substrate by a facile electrodeposition method, which can be an efficient and cheap bifunctional electrocatalyst for both the OER and HER and offer potential applications in the field of full water splitting.
Graphene oxide (GO) was found to effectively enhance the selectivity of aggregation-induced emission (AIE) biosensors, and a new method based on GO and AIE molecules was proposed to detect bovine serum albumin (BSA) with high sensitivity and selectivity.
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