| Literature DB >> 25815414 |
Benjamin Abécassis1, Cécile Bouet2, Cyril Garnero1, Doru Constantin1, Nicolas Lequeux2, Sandrine Ithurria2, Benoit Dubertret2, Brian Richard Pauw3, Diego Pontoni4.
Abstract
Understanding the formation mechanism of colloidal nanocrystals is of paramount importance in order to design new nanostructures and synthesize them in a predictive fashion. However, reliable data on the pathways leading from molecular precursors to nanocrystals are not available yet. We used synchrotron-based time-resolved in situ small and wide-angle X-ray scattering to experimentally monitor the formation of CdSe quantum dots synthesized in solution through the heating up of precursors in octadecene at 240 °C. Our experiment yields a complete movie of the structure of the solution from the self-assembly of the precursors to the formation of the quantum dots. We show that the initial cadmium precursor lamellar structure melts into small micelles at 100 °C and that the first CdSe nuclei appear at 218.7 °C. The size distributions and concentration in nanocrystals are measured in a quantitative fashion as a function of time. We show that a short nucleation burst lasting 30 s is followed by a slow decrease of nanoparticle concentration. The rate-limiting process of the quantum dot formation is found to be the thermal activation of selenium.Entities:
Keywords: CdSe; SAXS; mechanism; nanoparticle; nucleation; quantum dots
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Year: 2015 PMID: 25815414 DOI: 10.1021/acs.nanolett.5b00199
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189