Abstract
Patchy particles occupy an increasingly important space in soft matter research due to their ability to assemble into intricate phases and states. Being able to fine-tune the interactions among these particles is essential to understanding the principles governing the self-assembly processes. However, current fabrication techniques often yield patches that deviate chemically and physically from the native particles, impeding the identification of the driving forces behind self-assembly. To overcome this challenge, we propose a new approach to synthesizing spherical colloids with a well-defined rough patch on their surface. By treating polystyrene microspheres with vapors of a good solvent, here an acetone-water mixture, we achieve selective polymer corrugation on the particle surface resulting in a chemically similar yet rough surface patch. The key step is the selective condensation of the acetone-water vapors on the apex of the polystyrene microparticles immobilized on a substrate, which leads to rough patch formation. We leverage the ability to tune the vapor-liquid equilibrium of the volatile acetone-water mixture to precisely control the polymer corrugation on the particle surface. We demonstrate the dependence of patch formation on particle and substrate wettability, with the condensation occurring on the particle apex only when it is more wettable than the substrate, which is consistent with Volmer’s classical nucleation theory. By combining experiments and molecular dynamics simulations, we identify the role of the rough patch in the depletion interaction-driven self-assembly of the microspheres, which is crucial for designing programmable supracolloidal structures.
| Original language | English |
|---|---|
| Pages (from-to) | 1107-1117 |
| Number of pages | 11 |
| Journal | JACS Au |
| Volume | 4 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 25 2024 |
| Externally published | Yes |
Funding
The authors thank Dr. J. Chun and Dr. E. Nakouzi at Pacific Northwest National Laboratory (PNNL) for useful discussions. They acknowledge J. N. L. Albert, N. S. Pesika, and D. F. Shantz of the Chemical and Biomolecular Engineering Department at Tulane University for use of their Bruker Dimension FastScan atomic force microscope, associated financial support from the Louisiana Board of Regents Support Fund Contract #LEQSF(2019-20)-ENH-DE-21. They extend special thanks to Roya Gadimli for providing training and support during our use of the instrument. The authors also thank LSU’s Nano Fabrication Facility (NFF) for additional AFM measurements. B.B. acknowledges the financial support from National Science Foundation under grants CBET-1943986 (NSF-CAREER) and CBET-2038305.
Keywords
- colloidal assembly
- condensation
- directed assembly
- molecular dynamics
- patchy particles
- surface interactions
- vapor−liquid equilibria