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Increased Propensity of I-aq(-) for the Water Surface in Non-neutral Solutions: Implications for the Interfacial Behavior of H3Oaq+ and OHaq-
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Surface and Interface Science.
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Molecular and condensed matter physics.
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Surface and Interface Science.
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2011 (English)In: The Journal of Physical Chemistry Letters, ISSN 1948-7185, Vol. 2, no 9, 972-976 p.Article in journal (Refereed) Published
Abstract [en]

By a combination of surface-sensitive photoelectron spectroscopy and molecular dynamics simulations, we characterize the surface propensity of the iodide anion in aqueous solutions at acidic, neutral, and basic conditions (pH = 1, 6.8 and 13). In both experiments and simulations, an increased surface concentration of I- is found in non-neutral solutions. We interpret these findings in terms of I- surface coadsorption with hydronium at low pH and "salting out" of iodide by hydroxide from the bulk solution to the surface at high pH. The present study is thus in accord with the picture of a weak surface adsorption of hydronium and surface depletion of hydroxide, being in sharp contradiction with the interpretation of electrophoretic and titration measurements in terms of strong surface enrichment of OH-.

Place, publisher, year, edition, pages
2011. Vol. 2, no 9, 972-976 p.
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Physical Sciences
Identifiers
URN: urn:nbn:se:uu:diva-153959DOI: 10.1021/jz2003233ISI: 000290372900009OAI: oai:DiVA.org:uu-153959DiVA: diva2:418557
Available from: 2011-05-23 Created: 2011-05-23 Last updated: 2016-04-12

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Söderström, Johan

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