Evaporating droplets of colloidal dispersions on superamphiphobic surfaces is a versatile way to fabricate supraparticles with complex shape and internal morphology. Here, we investigated experimentally the formation of supraparticles consisting of polystyrene (PS) ellipsoids, with aspect ratios ranging from 4 to 11, and of sphere-ellipsoid mixtures. We demonstrated that the final supraparticle morphology can be tuned from buckled to spherical through the addition of the surfactant sodium dodecyl sulfate (SDS), which stabilizes the colloids within the drying droplet. At low evaporation speeds, we observed the ordering of the ellipsoidal colloids into small nematic bundles inside the supraparticle and into smectic domains on the supraparticle surface, which is consistent with results from previous computer simulations. The orientational ordering of ellipsoidal colloids was disrupted in the binary supraparticles consisting of sphere-ellipsoid mixtures, even at low sphere concentrations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.langmuir.5c00409 | DOI Listing |
Langmuir
March 2025
Department of Physics at Interfaces, Max-Planck Institute for Polymer Research, 55128 Mainz, Germany.
Evaporating droplets of colloidal dispersions on superamphiphobic surfaces is a versatile way to fabricate supraparticles with complex shape and internal morphology. Here, we investigated experimentally the formation of supraparticles consisting of polystyrene (PS) ellipsoids, with aspect ratios ranging from 4 to 11, and of sphere-ellipsoid mixtures. We demonstrated that the final supraparticle morphology can be tuned from buckled to spherical through the addition of the surfactant sodium dodecyl sulfate (SDS), which stabilizes the colloids within the drying droplet.
View Article and Find Full Text PDFLangmuir
October 2024
Institute of Physical Chemistry, University of Hamburg, Grindelallee 117, 20146 Hamburg, Germany.
Soft Matter
September 2024
Harvard John A. Paulson School of Engineering and Applied Sciences, 150 Western Ave., Boston MA 02134, USA.
Hierarchically structured supraparticles can be produced by drying droplets of colloidal suspensions. Using binary suspensions provides degrees of structural and functional control beyond those possible for single components, while remaining tractable for fundamental mechanistic studies. Here, we implement evaporative co-assembly of two distinct particle types - 'large' polystyrene microparticles and 'small' inorganic oxide nanoparticles (silica, titania, zirconia, or ceria) - dried on superhydrophobic surfaces to produce bowl-shaped supraparticles.
View Article and Find Full Text PDFWe report on the synthesis of hybrid light emitting particles with a diameter ranging between 100 and 500 nm, consisting in a compact semiconductor CdSe/CdS/CdZnS nanocrystal aggregate encapsulated by a controlled nanometric size silica and gold layers. We first characterize the Purcell decay rate enhancement corresponding to the addition of the gold nanoshell as a function of the particle size and find a good agreement with the predictions of numerical simulations. Then, we show that the contribution corresponding to Förster resonance energy transfer is inhibited.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
October 2021
Institute of Particle Technology, Friedrich-Alexander University Erlangen-Nürnberg, Cauerstrasse 4, 91058 Erlangen, Germany.
Colloidal supraparticles are micron-scale spherical assemblies of uniform primary particles, which exhibit emergent properties of a colloidal crystal, yet exist as a dispersible powder. A prerequisite to utilize these emergent functionalities is that the supraparticles maintain their mechanical integrity upon the mechanical impacts that are likely to occur during processing. Understanding how the internal structure relates to the resultant mechanical properties of a supraparticle is therefore of general interest.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!