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Water Structuring and Hydroxide Ion Binding at the Interface between Water and Hydrophobic Walls of Varying Rigidity and van der Waals Interactions

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Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic and Center for Biomolecules and Complex Molecular Systems, Flemingovo nám. 2, 16610 Prague 6, Czech Republic, Contribution from the GBB Institute, Department of Biophysical Chemistry, and Stratingh Institute, Physical Organic Chemistry Unit, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands
* Corresponding author. E-mail: [email protected]; FAX: +420-220 410 320.
†Academy of Sciences of the Czech Republic and Center for Biomolecules and Complex Molecular Systems.
‡University of Groningen.
Cite this: J. Phys. Chem. C 2008, 112, 20, 7689–7692
Publication Date (Web):April 30, 2008
https://doi.org/10.1021/jp800888b
Copyright © 2008 American Chemical Society
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    Abstract

    The interfacial behavior of hydroxide ions has been investigated by means of molecular dynamics simulations of aqueous KOH solutions between hydrophobic carbon-like walls. In agreement with previous calculations, we show that a rigid, attractive wall strongly structures water molecules in neighboring hydration layers, leading to a concentration peak of hydrated OH− ions located about 5 Å from the wall. However, allowing for thermal motion of the wall atoms, as well as suppressing the van der Waals interactions between the wall and water hydrogen atoms, strongly reduces both water structuring and the anionic peak in the interfacial region. We infer that soft hydrophobic environments with weak dispersion interactions with water are not expected to exhibit an appreciable structuring effect on interfacial water molecules. Hence, the mechanism for OH− adsorption operative near a hard attractive wall may not be applicable to soft aqueous interfaces, including the limiting case of the water/air interface.

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