4.6 Article

Phosphine-Free Synthesis of High-Quality CdSe Nanocrystals in Noncoordination Solvents: Activating Agent and Nucleating Agent Controlled Nucleation and Growth

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 113, Issue 20, Pages 8701-8709

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp811308h

Keywords

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Funding

  1. National Natural Science Foundation of China [90713022]
  2. National Key Basic Research Development Project of China [2007CB714500]
  3. Project of Chinese Academy of Sciences [KJCX2.YW.H09, KJCX2.YW.H11]

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CdSe nanocrystals (NCs) are prepared in noncoordination solvents (1-octadecene (ODE) and paraffin liquid) with Ion g-chain primary alkylamine as the sole ligand, ODE-Se, and cadmium fatty acid salt as precursors. The obtained NCs meet the four fundamental parameters for high-quality NCs: high crystallinity, narrow size distribution, moderate photoluminescence quantum yield, and broad range size tunableness. Further, by simply regulating the relative molar ratio of alkylamine to cadmium precursor, the regular sized nuclei and final obtained NCs can be produced predictably within a certain size range. The size distribution of regular sized nuclei is very narrow (fwhm = 23 +/- 1 nm), and the following focusing growth procedure vanishes. This indicates a different nucleation and growth kinetics from that of the well-established focusing and defocusing theory. By analyzing the conversion factor of precursors and the concentration of magic sized nanoclusters and regular sized nuclei, a subtle secondary nucleation mechanism, quantized fusion, was proposed. First, magic sized nanoclusters are formed as the critical nuclei; second, quantized critical nuclei will couple together and fuse into perfect regular sized nuclei by combining with stoichiometric monomers. The quantized fusion transformation could be regulated by the nature and ratios of the activating agent and the nucleating agent. These transition processes are very rapid and should be kinetically controlled. The molecular mechanism for monomer formation may be based on the traditional ester aminolysis reaction.

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