Interaction Heterogeneity can Favorably Impact Colloidal Crystal Nucleation

被引:9
|
作者
Jenkins, Ian C. [1 ]
Crocker, John C. [1 ]
Sinno, Talid [1 ]
机构
[1] Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
DNA-COATED COLLOIDS; PROGRAMMABLE NANOPARTICLE CRYSTALLIZATION; PHASE-BEHAVIOR; DYNAMICS; KINETICS; TRANSFORMATIONS; ATTRACTION; SIMULATION; PARTICLES; GELATION;
D O I
10.1103/PhysRevLett.119.178002
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Colloidal particles with short-ranged attractions, e.g., micron-scale spheres functionalized with single-stranded DNA oligomers, are susceptible to becoming trapped in disordered configurations even when a crystalline arrangement is the ground state. Moreover, for reasons that are not well understood, seemingly minor variations in the particle formulation can lead to dramatic changes in the crystallization outcome. We demonstrate, using a combination of equilibrium and nonequilibrium computer simulations, that interaction heterogeneity-variations in the energetic interactions among different particle pairs in the population-may favorably impact crystal nucleation. Specifically, interaction heterogeneity is found to lower the free energy barrier to nucleation via the formation of clusters comprised preferentially of strong-binding particle pairs. Moreover, gelation is inhibited by "spreading out over time" the nucleation process, resulting in a reduced density of stable nuclei, allowing each to grow unhindered and larger. Our results suggest a simple and robust approach for enhancing colloidal crystallization near the "sticky sphere" limit, and support the notion that differing extents of interaction heterogeneity arising from various particle functionalization protocols may contribute to the otherwise unexplained variations in crystallization outcomes reported in the literature.
引用
收藏
页数:6
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