4.8 Article

Direct Observation of Nanoparticle Superlattice Formation by Using Liquid Cell Transmission Electron Microscopy

Journal

ACS NANO
Volume 6, Issue 3, Pages 2078-2085

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn203837m

Keywords

nanoparticle; self-assembly; in situ liquid cell TEM; platinum; coarse-grained modeling

Funding

  1. Physical Chemistry of Semiconductor Nanocrystals Program [KC3105]
  2. Office of Science, Office of Basic Energy Sciences, of the United States Department of Energy [DE-AC02-05CH11231]
  3. FP7Marie Curie IOF project HJSC
  4. Miller Institute for Basic Research in Science at UC Berkeley
  5. Lawrence Berkeley National Lab
  6. U.S. Department of Energy [DE-AC02-05CH11231]
  7. National Center for Electron Microscopy
  8. Office of Science, Office of Basic Energy Sciences, Materials Science and Engineering Division of the U.S. Department of Energy [DE-AC02-05CH11231]

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Direct imaging of nanoparticle solutions by liquid phase transmission electron microscopy has enabled unique in situ studies of nanoparticle motion and growth. In the present work, we report on real-time formation of two-dimensional nanoparticle arrays in the very low diffusive limit, where nanoparticles are mainly driven by capillary forces and solvent fluctuations. We find that superlattice formation appears to be segregated into multiple regimes. Initially, the solvent front drags the nanoparticles, condensing them Into an amorphous agglomerate. Subsequently, the nanoparticle crystallization into an array is driven by local fluctuations. Following the crystallization event, superlattice growth can also occur via the addition of individual nanoparticles drawn from outlying regions by different solvent fronts. The dragging mechanism is consistent with simulations based on a coarse-grained lattice gas model at the same limit.

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