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Updated: Dec 18, 2025

Synthesis and Characterization of Supramolecular Colloids
Published on: April 22, 2016
Self-assembly of finite-sized colloidal aggregates
Pritam Kumar Jana1, Bortolo Matteo Mognetti
1Université Libre de Bruxelles (ULB), Interdisciplinary Center for Nonlinear Phenomena and Complex Systems, Campus Plaine, CP 231, Blvd. du Triomphe, B-1050 Brussels, Belgium. Pritam.Kumar.Jana@ulb.ac.be Bortolo.Matteo.Mognetti@ulb.be.
Researchers developed a versatile method for precise colloidal self-assembly using DNA linkers. This approach controls the formation of specific aggregate structures, like molecules and clusters, from bulk suspensions.
Area of Science:
- Colloid science
- Materials science
- Biophysics
Background:
- Precise control over colloidal aggregate morphology is challenging.
- Microfluidic platforms offer solutions by precise particle loading.
- Existing methods require exact positioning to avoid off-target structures.
Purpose of the Study:
- To validate a versatile design for fabricating diverse finite-sized colloidal aggregates.
- To demonstrate control over aggregate morphology using tunable DNA-mediated interactions.
- To explore the formation of colloidal molecules and core-shell clusters from bulk suspensions.
Main Methods:
- Theoretical modeling and simulations of colloidal interactions.
- Utilizing DNA linkers with mobile tethering points for particle interaction.
- Investigating systems with DNA oligomers and hydrophobic complexes in supported bilayers.
- Fine-tuning linker strength and number to control aggregate formation.
Main Results:
- Successful fabrication of various finite-sized aggregates, including colloidal molecules and core-shell clusters.
- Demonstrated control over aggregate morphology, specifically molecular valency and cluster size.
- Validated a versatile design for self-assembly from finite density suspensions.
- Showcased how multivalent interactions drive microphase separation under equilibrium.
Conclusions:
- The proposed design offers a versatile approach to colloidal self-assembly.
- Tunable DNA-mediated interactions are key to controlling aggregate morphology.
- Multivalent interactions can effectively induce microphase separation in equilibrium systems.
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