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- W3016189615 startingPage "4451" @default.
- W3016189615 abstract "In this work, we show how and why the interactions between charged cubic colloids range from radially isotropic to strongly directionally anisotropic, depending on tuneable factors. Using molecular dynamics simulations, we illustrate the effects of typical solvents to complement experimental investigations of cube assembly. We find that in low-salinity water solutions, where cube self-assembly is observed, the colloidal shape anisotropy leads to the strongest attraction along the corner-to-corner line, followed by edge-to-edge, with a face-to-face configuration of the cubes only becoming energetically favorable after the colloids have collapsed into the van der Waals attraction minimum. Analysing the potential of mean force between colloids with varied cubicity, we identify the origin of the asymmetric microstructures seen in experiment." @default.
- W3016189615 created "2020-04-17" @default.
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- W3016189615 date "2020-01-01" @default.
- W3016189615 modified "2023-10-18" @default.
- W3016189615 title "Self-assembly of charged colloidal cubes" @default.
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- W3016189615 doi "https://doi.org/10.1039/c9sm02189b" @default.
- W3016189615 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32323672" @default.
- W3016189615 hasPublicationYear "2020" @default.
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