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Laurent Coolen

Researcher at Pierre-and-Marie-Curie University

Publications -  35
Citations -  656

Laurent Coolen is an academic researcher from Pierre-and-Marie-Curie University. The author has contributed to research in topics: Quantum dot & Plasmon. The author has an hindex of 12, co-authored 35 publications receiving 613 citations. Previous affiliations of Laurent Coolen include Centre national de la recherche scientifique.

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Measurement of the Radiative and Nonradiative Decay Rates of Single CdSe Nanocrystals through a Controlled Modification of their Spontaneous Emission

TL;DR: The results demonstrate that the fluorescence quantum efficiency, determined at the single-molecule level, is 98% in average, far above the value expected from conventional ensemble experiments.
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Emission characterization of a single CdSe-ZnS nanocrystal with high temporal and spectral resolution by photon-correlation Fourier spectroscopy.

TL;DR: A spectroscopic study of single colloidal CdSe/ZnS nanocrystals at low temperature using photon-correlation Fourier spectroscopy, a technique based on measuring the correlations of the intensities detected at the outputs of a Michelson interferometer.
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Emission properties of single CdSe/ZnS quantum dots close to a dielectric interface

TL;DR: In this paper, the effect of a dielectric interface on the emission of individual semiconductor quantum dots (QDs) was studied by placing a single nanoparticle successively close and far from an interface, enabling a direct comparison of its fluorescence properties.
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Controlled modification of single colloidal CdSe/ZnS nanocrystal fluorescence through interactions with a gold surface

TL;DR: Single colloidal CdSe/ZnS nanocrystals are deposited at various distances from a gold film in order to improve their performance as single photon sources andPhoton antibunching is demonstrated and the experimental curves are accurately fitted by theoretical equations.
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Photon-correlation Fourier spectroscopy.

TL;DR: A method to probe the spectral fluctuations of a transition over broad ranges of frequencies and timescales with the high spectral resolution of Fourier spectroscopy, and a temporal resolution as high as the excited state lifetime, even in the limit of very low photocounting rates.