Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile; Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.
Hamburg University of Technology, Institute of Polymers and Composites, 21073 Hamburg, Germany.
J Colloid Interface Sci. 2022 Jan 15;606(Pt 1):57-66. doi: 10.1016/j.jcis.2021.07.121. Epub 2021 Jul 26.
Weakly bound, physisorbed hydrocarbons could in principle provide a similar water-repellency as obtained by chemisorption of strongly bound hydrophobic molecules at surfaces.
Here we present experiments and computer simulations on the wetting behaviour of water on molecularly thin, self-assembled alkane carpets of dotriacontane (n-CH or C32) physisorbed on the hydrophilic native oxide layer of silicon surfaces during dip-coating from a binary alkane solution. By changing the dip-coating velocity we control the initial C32 surface coverage and achieve distinct film morphologies, encompassing homogeneous coatings with self-organised nanopatterns that range from dendritic nano-islands to stripes.
These patterns exhibit a good water wettability even though the carpets are initially prepared with a high coverage of hydrophobic alkane molecules. Using in-liquid atomic force microscopy, along with molecular dynamics simulations, we trace this to a rearrangement of the alkane layers upon contact with water. This restructuring is correlated to the morphology of the C32 coatings, i.e. their fractal dimension. Water molecules displace to a large extent the first adsorbed alkane monolayer and thereby reduce the hydrophobic C32 surface coverage. Thus, our experiments evidence that water molecules can very effectively hydrophilize initially hydrophobic surfaces that consist of weakly bound hydrocarbon carpets.
弱结合、物理吸附的碳氢化合物原则上可以提供类似于强结合疏水分子在表面化学吸附所获得的疏水性。
在这里,我们进行了实验和计算机模拟,研究了在亲水自然氧化层硅表面上通过从二元烷烃溶液中浸涂来物理吸附三十二烷(n-CH 或 C32)分子薄自组装烷烃地毯的水在表面上的润湿行为。通过改变浸涂速度,我们可以控制初始 C32 表面覆盖率,并实现不同的薄膜形态,包括具有自组织纳米图案的均匀涂层,范围从树枝状纳米岛到条纹。
尽管地毯最初用高覆盖率的疏水性烷烃分子制备,但这些图案表现出良好的润湿性。使用液中原子力显微镜以及分子动力学模拟,我们追踪到这与接触水时烷烃层的重排有关。这种重构与 C32 涂层的形态,即其分形维数相关。水分子在很大程度上取代了第一层吸附的烷烃单层,从而降低了疏水性 C32 表面覆盖率。因此,我们的实验证明,水分子可以非常有效地水合由弱结合碳氢化合物地毯组成的最初疏水性表面。