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ACS Nano. 2012 Oct 23;6(10):8599-610. doi: 10.1021/nn303371y. Epub 2012 Sep 13.

Direct in situ determination of the mechanisms controlling nanoparticle nucleation and growth.

Author information

1
Department of Chemical Engineering and Materials Science, University of California, Davis, Davis, California 95616, USA. tjwoehl@ucdavis.edu

Abstract

Although nanocrystal morphology is controllable using conventional colloidal synthesis, multiple characterization techniques are typically needed to determine key properties like the nucleation rate, induction time, growth rate, and the resulting morphology. Recently, researchers have demonstrated growth of nanocrystals by in situ electron beam reduction, offering direct observations of single nanocrystals and eliminating the need for multiple characterization techniques; however, they found nanocrystal morphologies consistent with two different growth mechanisms for the same electron beam parameters. Here we show that the electron beam current plays a role analogous to the concentration of reducing agent in conventional synthesis, by controlling the growth mechanism and final morphology of silver nanocrystals grown via in situ electron beam reduction. We demonstrate that low beam currents encourage reaction limited growth that yield nanocrystals with faceted structures, while higher beam currents encourage diffusion limited growth that yield spherical nanocrystals. By isolating these two growth regimes, we demonstrate a new level of control over nanocrystal morphology, regulated by the fundamental growth mechanism. We find that the induction threshold dose for nucleation is independent of the beam current, pixel dwell time, and magnification being used. Our results indicate that in situ electron microscopy data can be interpreted by classical models and that systematic dose experiments should be performed for all future in situ liquid studies to confirm the exact mechanisms underlying observations of nucleation and growth.

PMID:
22957797
PMCID:
PMC3482139
DOI:
10.1021/nn303371y
[Indexed for MEDLINE]
Free PMC Article

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