Abstract
We have employed amplitude- and phase-resolved second-harmonic generation spectroscopy to investigate ion-specific effects of monovalent cations at the fused silica:water interface maintained under acidic, neutral, and alkaline conditions. We find a negligible dependence of the total potential (as negative as −400 mV at pH 14), the second-order nonlinear susceptibility (as large as 1.5 × 10-21 m2 V-1 at pH 14), the number of Stern layer water molecules (1 × 1015 cm-2 at pH 5.8), and the energy associated with water alignment upon going from neutral to high pH (ca. −24 kJ mol-1 to −48 kJ mol-1 at pH 13 and 14, close to the cohesive energy of liquid water but smaller than that of ice) on chlorides of the alkali series (M+ = Li+, Na+, K+, Rb+, and Cs+). Attempts are presented to provide estimates for the molecular hyperpolarizability of the cations and anions in the Stern layer at high pH, which arrive at ca. 20-fold larger values for αtotal ions(2) = αM+(2) + αOH-(2) + αCl-(2) when compared to water’s molecular hyperpolarizability estimate from theory and point to a sizable contribution of deprotonated silanol groups at high pH. In contrast to the alkali series, a pronounced dependence of the total potential and the second-order nonlinear susceptibility on monovalent cationic (cetrimonium bromide, CTAB) and anionic (perfluorooctanoic and perfluorooctanesulfonic acid, PFOA and PFOS) surfactants was quantifiable. Our findings are consistent with a low surface coverage of the alkali cations and a high surface coverage of the surfactants. Moreover, they underscore the important contribution of Stern layer water molecules to the total potential and second-order nonlinear susceptibility. Finally, they demonstrate the applicability of heterodyne-detected second-harmonic generation spectroscopy for identifying perfluorinated acids at mineral:water interfaces.
Original language | English (US) |
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Pages (from-to) | 8404-8414 |
Number of pages | 11 |
Journal | Journal of Physical Chemistry A |
Volume | 127 |
Issue number | 40 |
DOIs | |
State | Published - Oct 12 2023 |
Funding
This work was supported by the U.S. National Science Foundation (CHE-2153191), the Air Force Office of Scientific Research (FA9550-16-1-0379), and the Department of Energy (DE-SC0023342). E.H.L. acknowledges a Buffett Global Impacts Graduate Fellowship from the Roberta Buffett Institute for Global Affairs at Northwestern University. F.M.G. designed the experiment. H.C., E.M., and E.H.L. carried out the experiments. H.C., E.M., E.H.L., and F.M.G. analyzed the data and wrote the manuscript.
ASJC Scopus subject areas
- Physical and Theoretical Chemistry