4.8 Article

Free Energy Landscape of Colloidal Clusters in Spherical Confinement

期刊

ACS NANO
卷 13, 期 8, 页码 9005-9015

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b03039

关键词

self-assembly; hard spheres; supraparticles; emulsions; magic numbers; icosahedral symmetry; defects

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [EN 905/2-1, VO 1824/7-1]
  2. DFG [GRK 1896]
  3. Cluster of Excellence Engineering of Advanced Materials Grant [EXC 315/2]
  4. Erlangen Regional Computing Center (RRZE)

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The structure of finite self -assembling systems depends sensitively on the number of constituent building blocks. Recently, it was demonstrated that hard sphere -like colloidal particles show a magic number effect when confined in emulsion droplets. Geometric construction rules permit a few dozen magic numbers that correspond to a discrete series of completely filled concentric icosahedral shells. Here, we investigate the free energy landscape of these colloidal clusters as a function of the number of their constituent building blocks for system sizes up to several thousand particles. We find that minima in the free energy landscape, arising from the presence of filled, concentric shells, are significantly broadened, compared to their atomic analogues. Colloidal clusters in spherical confinement can flexibly accommodate excess particles by ordering icosahedrally in the cluster center while changing the structure near the cluster surface. In between these magic number regions, the building blocks cannot arrange into filled shells. Instead, we observe that defects accumulate in a single wedge and therefore only affect a few tetrahedral grains of the cluster. We predict the existence of this wedge by simulation and confirm its presence in experiment using electron tomography. The introduction of the wedge minimizes the free energy penalty by confining defects to small regions within the cluster. In addition, the remaining ordered tetrahedral grains can relax internal strain by breaking icosahedral symmetry. Our findings demonstrate how multiple defect mechanisms collude to form the complex free energy landscape of colloidal clusters.

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