TUHH Open Research
Help
  • Log In
    New user? Click here to register.Have you forgotten your password?
  • English
  • Deutsch
  • Communities & Collections
  • Publications
  • Research Data
  • People
  • Institutions
  • Projects
  • Statistics
  1. Home
  2. TUHH
  3. Publication References
  4. How water wets and self-hydrophilizes nanopatterns of physisorbed hydrocarbons
 
Options

How water wets and self-hydrophilizes nanopatterns of physisorbed hydrocarbons

Publikationstyp
Journal Article
Date Issued
2022-01-15
Sprache
English
Author(s)
Diaz, Diego I.  
Nickel, Ole  
Moraga, Nicolas H.  
Catalan, Rodrigo E.  
Retamal, Maria Jose  
Zelada, Hugo  
Cisternas, Marcelo A.  
Meißner, Robert  orcid-logo
Huber, Patrick  orcid-logo
Corrales, Tomas P.  
Volkmann, Ulrich G.  
Institut
Kunststoffe und Verbundwerkstoffe M-11  
Material- und Röntgenphysik M-2  
Molekulardynamische Simulation weicher Materie M-EXK2  
TORE-URI
http://hdl.handle.net/11420/10175
Journal
Journal of colloid and interface science  
Volume
606
Issue
1
Start Page
57
End Page
66
Citation
Journal of Colloid and Interface Science 606 (1): 57-66 (2022-01-15)
Publisher DOI
10.1016/j.jcis.2021.07.121
Scopus ID
2-s2.0-85112127438
Publisher
Elsevier
Hypothesis: Weakly bound, physisorbed hydrocarbons could in principle provide a similar water-repellency 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 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.
Subjects
Atomic force microscopy
Electron microscopy
Molecular dynamics simulation
n-Alkane
Silica
Silicon
Wetting
DDC Class
600: Technik
Funding(s)
GRK 2462: Teilprojekt B1 Selbstdiffusion und Transport von molekularen Flüssigkeiten in granularen Packungen aus mesoporösen Silikat- und Aerogel-Pulvern  
SFB 986: Teilprojekt B7 - Polymere in grenzflächenbestimmten Geometrien: Struktur, Dynamik und Funktion an planaren und in porösen Hybridsystemen  
SFB 986: Teilprojekt B10 - Funktionalisierung von hierarchischen nanoporösen Metallen durch aktive organische Filme  
DASHH Helmholtz Graduiertenkolleg  
Funding Organisations
Deutsche Forschungsgemeinschaft (DFG)  
More Funding Information
UGV acknowledges support of Fondecyt 1180939. TPC acknowledges the support of Fondecyt Iniciación 11160664, PCI MPG190023. PH acknowledges support by the Deutsche Forschungsgemeinschaft (DFG) within the priority program SPP 2171, “Dynamic wetting of flexible, adaptive and switchable surfaces”, Projektnummer 22879465.
TUHH
Weiterführende Links
  • Contact
  • Send Feedback
  • Cookie settings
  • Privacy policy
  • Impress
DSpace Software

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science
Design by effective webwork GmbH

  • Deutsche NationalbibliothekDeutsche Nationalbibliothek
  • ORCiD Member OrganizationORCiD Member Organization
  • DataCiteDataCite
  • Re3DataRe3Data
  • OpenDOAROpenDOAR
  • OpenAireOpenAire
  • BASE Bielefeld Academic Search EngineBASE Bielefeld Academic Search Engine
Feedback