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Self-assembled surfactants on patterned surfaces: confinement and cooperative effects on aggregate morphology

机译:图案表面上的自组装表面活性剂:对聚集体形态的限制和协同作用

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The adsorption and self-assembly of surfactants are ubiquitous processes in several technological applications, including the manufacture of nano-structured materials using bottom-up strategies. Although much is known about the adsorption of surfactants on homogeneous flat surfaces from experiments, theory, and simulations, limited information is available, in quantifiable terms, regarding the adsorption of surfactants on surfaces with chemical and/or morphological heterogeneity. In an effort to fill this knowledge gap, we report here results obtained using equilibrium dissipative particle dynamics (DPD) simulations for the adsorption of model surfactants onto patterned flat surfaces [i.e., flat surfaces with chemical heterogeneity). The patterns consist of one or two stripes of variable width on which the surfactants could adsorb. The adsorbing stripes are surrounded by a surface that effectively repels the surfactants. This repelling surface, perhaps not realistic, allows us to quantify the effect of lateral confinement on the morphology of surfactant aggregates. When the stripe width is large (effectively providing a homogeneous flat surface), the surfactants yield a flat monolayer. Our simulations suggest that the flat monolayers become hemi-cylinders, hemi-spheres, and individual surfactants as the stripe width decreases, a consequence of lateral confinement. In some cases our simulations show evidence of cooperative effects when two adsorbing stripes are present on the surface. If the distance between the stripes and the widths of the stripes are both less than about one surfactant length, hemi-cylindrical shells and irregular structures are observed because of cooperativity; otherwise the results match those found for a single isolated stripe. Our predictions could be useful for the design of new nano-structured materials and coatings, for applications ranging from nano-fluidic devices to nano-reactors.
机译:在几种技术应用中,表面活性剂的吸附和自组装是无处不在的过程,包括使用自下而上的策略制造纳米结构材料。尽管从实验,理论和模拟方面对表面活性剂在均相平坦表面上的吸附知之甚少,但是在定量方面,关于表面活性剂在具有化学和/或形态异质性的表面上的吸附信息有限。为了填补这一知识空白,我们在这里报告使用平衡耗散粒子动力学(DPD)模拟将模型表面活性剂吸附到带图案的平坦表面(即具有化学异质性的平坦表面)上获得的结果。该图案由表面活性剂可吸附在其上的一或两个可变宽度的条带组成。吸附条被有效排斥表面活性剂的表面包围。这种排斥的表面,也许是不现实的,使我们能够量化侧向限制对表面活性剂聚集体形态的影响。当条带宽度大时(有效地提供均匀的平坦表面),表面活性剂会产生平坦的单层。我们的模拟表明,随着条带宽度的减小,平坦的单分子层变成半圆柱,半球和单个表面活性剂,这是横向约束的结果。在某些情况下,当表面上存在两个吸附条纹时,我们的模拟显示了协同效应的证据。如果条纹之间的距离和条纹的宽度均小于约一个表面活性剂长度,则由于协同作用,观察到半圆柱形壳和不规则结构;反之,否则结果与在单个隔离条中找到的结果匹配。我们的预测可能对设计新型纳米结构材料和涂层,从纳米流体装置到纳米反应器的应用很有用。

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