成核
材料科学
棒
旋节分解
化学物理
Crystal(编程语言)
过饱和度
旋节
胶体
聚合物
相(物质)
结晶
星团(航天器)
结晶学
热力学
化学工程
复合材料
化学
物理
计算机科学
替代医学
工程类
病理
有机化学
医学
程序设计语言
作者
Alessandro Patti,Marjolein Dijkstra
标识
DOI:10.1103/physrevlett.102.128301
摘要
We study the isotropic-to-crystal transformation in a mixture of colloidal hard rods and nonabsorbing polymer using computer simulations. We determine the height of the nucleation barrier and find that the critical cluster consists of a single crystalline layer growing laterally for all polymer fugacities considered. At lower supersaturation, the free energy of a single hexagonally packed layer increases monotonically with size, while the nucleation barrier of a second crystalline layer is extremely high. Hence, the nucleation of multilayer crystals is never observed. Multilayer crystals form only in the spinodal decomposition regime, either where, in an intermediate stage, single crystalline membranes coalesce into multilayer clusters or where, at higher polymer fugacity, smaller clusters of rods stack on top of each other to form long filaments. Eventually, these transient structures evolve into a thermodynamically stable bulk crystal phase.
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