How water wets and self-hydrophilizes nanopatterns of physisorbed hydrocarbons

Diaz, Diego; Nickel, Ole; Moraga, Nicolas; Catalan, Rodrigo E.; Retamal, Maria Jose; Zelada, Hugo; Cisternas, Marcelo; Meissner, Robert; Huber, Patrick; Corrales, Tomas P.; Volkmann, Ulrich G.

Abstract

Hypothesis: Weakly bound, physisorbed hydrocarbons could in principle provide a similar waterrepellency as obtained by chemisorption of strongly bound hydrophobic molecules at surfaces. Experiments: Here we present experiments and computer simulations on the wetting behaviour of water on molecularly thin, self-assembled alkane carpets of dotriacontane (n-C32H66 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. Findings: 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 dimen-sion. 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. (c) 2021 Elsevier Inc. All rights reserved.

Más información

Título según WOS: How water wets and self-hydrophilizes nanopatterns of physisorbed hydrocarbons
Título de la Revista: JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volumen: 606
Editorial: ACADEMIC PRESS INC ELSEVIER SCIENCE
Fecha de publicación: 2022
Página de inicio: 57
Página final: 66
DOI:

10.1016/j.jcis.2021.07.121

Notas: ISI