Annealing cycles and the self-organization of functionalized colloids
arXiv:1710.02373 · doi:10.1088/1361-648X/aa9c0e
Abstract
The self-assembly of functionalized (patchy) particles with directional interactions into target structures is still a challenge, despite the significant experimental advances on their synthesis. The self-assembly pathways are typically characterized by high energy barriers that hinder the access to stable (equilibrium) structures. A possible strategy to tackle this challenge is to perform annealing cycles. By periodically switching on and off the inter-particle bonds, one expects to smooth-out the kinetic pathways and favor the assembly of targeted structures. Preliminary results have shown that the efficiency of annealing cycles depends strongly on their frequency. Here, we study numerically how this frequency-dependence scales with the strength of the directional interactions (size of the patch ). We use analytical arguments to show that the scaling results from the statistics of a random walk in configurational space.
References in corpus (11)
- Colloidal Gels: Equilibrium and Non-Equilibrium Routes
- Equilibrium cluster phases and low-density arrested disordered states: The role of short-range attraction and long-range repulsion
- Observation of empty liquids and equilibrium gels in a colloidal clay
- Interaction potentials for soft and hard ellipsoids
- Numerical evidence for nucleated self-assembly of DNA brick structures
- Gel to glass transition in simulation of a valence-limited colloidal system
- Mobile linkers on DNA-coated colloids: valency without patches
- Kinetic control of the coverage of oil droplets by DNA-functionalised colloids
- Precursors of order in aggregates of patchy particles
- Nonequilibrium growth of patchy-colloid networks on substrates
- Mixtures of functionalized colloids on substrates