Annealing cycles and the self-organization of functionalized colloids

被引:2
作者
Dias, Cristovao S. [1 ,2 ]
Araujo, Nuno A. M. [1 ,2 ]
Telo da Gama, Margarida M. [1 ,2 ]
机构
[1] Univ Lisbon, Fac Ciencias, Ctr Fis Teor & Computac, P-1749016 Lisbon, Portugal
[2] Univ Lisbon, Dept Fis, Fac Ciencias, P-1749016 Lisbon, Portugal
关键词
self-assembly; annealing cycles; non-equilibrium dynamics; DNA NANOSTRUCTURES; DYNAMICS; PARTICLES; NANOPARTICLES; AGGREGATION; FABRICATION; SYSTEMS;
D O I
10.1088/1361-648X/aa9c0e
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
The self-assembly of functionalized (patchy) particles with directional interactions into target structures is still a challenge, despite the significant experimental advances in their synthesis. Self-assembly pathways are typically characterized by high energy barriers that hinder 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 sigma). We use analytical arguments to show that the scaling results from the statistics of a random walk in configurational space.
引用
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页数:5
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