Novak Ekaterina V, Pyanzina Elena S, Sánchez Pedro A, Kantorovich Sofia S
Ural Federal University, Lenin Av. 51, 620000, Ekaterinburg, Russia.
Helmholz-Zentrum Dresden-Rosendorf, Bautzner Landstrasse 400, 01328, Dresden, Germany.
Eur Phys J E Soft Matter. 2019 Dec 23;42(12):158. doi: 10.1140/epje/i2019-11924-6.
Unlike Stockmayer fluids, that prove to undergo gas-liquid transition on cooling, the system of dipolar hard or soft spheres without any additional central attraction so far has not been shown to have a critical point. Instead, in the latter, one observes diverse self-assembly scenarios. Crosslinking dipolar soft spheres into supracolloidal magnetic polymer-like structures (SMPs) changes the self-assembly behaviour. Moreover, aggregation in systems of SMPs strongly depends on the constituent topology. For Y- and X-shaped SMPs, under the same conditions in which dipolar hard spheres would form chains, the formation of very large loose gel-like clusters was observed (E. Novak et al., J. Mol. Liq. 271, 631 (2018)). In this work, using molecular dynamics simulations, we investigate the self-assembly in suspensions of four topologically different SMPs --chains, rings, X and Y-- whose monomers interact via Stockmayer potential. As expected, compact drop-like clusters are formed by SMPs in all cases if the central isotropic attraction is introduced, however, their shape and internal structure turn out to depend on the SMPs topology.
与已证明在冷却时会发生气-液转变的斯托克迈耶流体不同,到目前为止,没有任何额外中心吸引力的偶极硬球或软球系统尚未显示出具有临界点。相反,在后者中,可以观察到各种自组装情况。将偶极软球交联成超胶体磁性聚合物样结构(SMPs)会改变自组装行为。此外,SMPs系统中的聚集强烈依赖于组成拓扑结构。对于Y形和X形SMPs,在偶极硬球会形成链的相同条件下,观察到形成了非常大的松散凝胶状簇(E. 诺瓦克等人,《分子液体杂志》271, 631 (2018))。在这项工作中,我们使用分子动力学模拟研究了四种拓扑结构不同的SMPs(链、环、X形和Y形)悬浮液中的自组装,其单体通过斯托克迈耶势相互作用。正如预期的那样,如果引入中心各向同性吸引力,在所有情况下SMPs都会形成紧凑的滴状簇,然而,它们的形状和内部结构却取决于SMPs的拓扑结构。