IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v7y2016i1d10.1038_ncomms13064.html
   My bibliography  Save this article

Thermally-nucleated self-assembly of water and alcohol into stable structures at hydrophobic interfaces

Author

Listed:
  • Kislon Voïtchovsky

    (Durham University)

  • Daniele Giofrè

    (Institute of Materials, Ecole Polytechnique Fédérale de Lausanne)

  • Juan José Segura

    (Institute of Materials, Ecole Polytechnique Fédérale de Lausanne)

  • Francesco Stellacci

    (Institute of Materials, Ecole Polytechnique Fédérale de Lausanne
    Interfaculty Bioengineering Institute, Ecole Polytechnique Fédérale de Lausanne)

  • Michele Ceriotti

    (Institute of Materials, Ecole Polytechnique Fédérale de Lausanne)

Abstract

At the interface with solids, the mobility of liquid molecules tends to be reduced compared with bulk, often resulting in increased local order due to interactions with the surface of the solid. At room temperature, liquids such as water and methanol can form solvation structures, but the molecules remain highly mobile, thus preventing the formation of long-lived supramolecular assemblies. Here we show that mixtures of water with methanol can form a novel type of interfaces with hydrophobic solids. Combining in situ atomic force microscopy and multiscale molecular dynamics simulations, we identify solid-like two-dimensional interfacial structures that nucleate thermally, and are held together by an extended network of hydrogen bonds. On graphite, nucleation occurs above ∼35 °C, resulting in robust, multilayered nanoscopic patterns. Our findings could have an impact on many fields where water-alcohol mixtures play an important role such as fuel cells, chemical synthesis, self-assembly, catalysis and surface treatments.

Suggested Citation

  • Kislon Voïtchovsky & Daniele Giofrè & Juan José Segura & Francesco Stellacci & Michele Ceriotti, 2016. "Thermally-nucleated self-assembly of water and alcohol into stable structures at hydrophobic interfaces," Nature Communications, Nature, vol. 7(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13064
    DOI: 10.1038/ncomms13064
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms13064
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms13064?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13064. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.