How water wets and self-hydrophilizes nanopatterns of physisorbed hydrocarbons.

Atomic force microscopy Electron microscopy Molecular dynamics simulation Silica Silicon Wetting n-Alkane

Journal

Journal of colloid and interface science
ISSN: 1095-7103
Titre abrégé: J Colloid Interface Sci
Pays: United States
ID NLM: 0043125

Informations de publication

Date de publication:
15 Jan 2022
Historique:
received: 11 04 2021
revised: 22 07 2021
accepted: 23 07 2021
pubmed: 14 8 2021
medline: 6 11 2021
entrez: 13 8 2021
Statut: ppublish

Résumé

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-C 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.

Identifiants

pubmed: 34388573
pii: S0021-9797(21)01182-6
doi: 10.1016/j.jcis.2021.07.121
pii:
doi:

Substances chimiques

Water 059QF0KO0R
Silicon Z4152N8IUI

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

57-66

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Diego Díaz (D)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile; Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.

Ole Nickel (O)

Hamburg University of Technology, Institute of Polymers and Composites, 21073 Hamburg, Germany.

Nicolás Moraga (N)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.

Rodrigo E Catalán (RE)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.

María José Retamal (MJ)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.

Hugo Zelada (H)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.

Marcelo Cisternas (M)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.

Robert Meißner (R)

Hamburg University of Technology, Institute of Polymers and Composites, 21073 Hamburg, Germany; Helmholtz-Zentrum Hereon, Institute of Surface Science, 21494 Geesthacht, Germany.

Patrick Huber (P)

Hamburg University of Technology, Institute for Materials and X-Ray Physics, 21073 Hamburg, Germany; Deutsches Elektronen-Synchrotron DESY, Centre for X-Ray and Nano Science CXNS, 22603 Hamburg, Germany; University of Hamburg, Centre for Hybrid Nanostructures CHyN, 22607 Hamburg, Germany. Electronic address: patrick.huber@tuhh.de.

Tomas P Corrales (TP)

Departamento de Física, Universidad Técnica Federico Santa María, Valparaiso 2390123, Chile. Electronic address: tomas.corrales@usm.cl.

Ulrich G Volkmann (UG)

Instituto de Física, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile; Centro de Investigación en Nanotecnología y Materiales Avanzados (CIEN-UC), Pontificia Universidad Católica de Chile, Santiago 7820436, Chile. Electronic address: volkmann@fis.puc.cl.

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