Abstract
The intrinsic high diffusion rate of colloids at low Péclet number results in an extremely fast crystallization process and instant formation of colloidal crystals, even at an ultracentrifugal field of extremely high intensity. By introducing a small number of clusters in sedimention, it should be possible to slow down the crystallization process, thus making the assembly order tunable in preparative ultracentrifugation experiments. Here, we used sodium dodecyl sulfate-stabilized polystyrene nanoparticles (with a size dispersity of 1.07) dispersed in a solution of high ionic strength. Sedimentation and assembly of these nanoparticles were done using preparative ultracentrifugation at various angular velocities. The sedimentation process was also analyzed in situ by analytical ultracentrifugation in real time. By creating as low as 3% of clusters into these nearly uniformly sized polystyrene nanoparticle dispersions during the sedimentation process, the superstructure order becomes easily tunable between glassy and crystalline. Theoretical calculations complemented the experiments to explain the mechanism of cluster formation in sedimentation. This work provides a novel methodology to produce superstructures with a tunable packing order for colloids at low Péclet number.
Original language | English |
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Pages (from-to) | 8752–8758 |
Number of pages | 7 |
Journal | Journal of Physical Chemistry C |
Volume | 125 |
Issue number | 16 |
DOIs | |
Publication status | Published - 15 Apr 2021 |
Bibliographical note
Funding Information:The authors would like to acknowledge the financial support from the EU H2020-MSCA-ITN-2015 project “MULTIMAT” (project number: 676045). The authors would also like to thank Jülich Centre for Neutron Science JCNS at MLZ for VSANS beamtime at KWS-3.
Publisher Copyright:
© 2021 American Chemical Society. All rights reserved.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.