Chemical Potential Driven Reorganization of Anions between Stern and Diffuse Layers at the Air/Water Interface

05 August 2021, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Ion adsorption and transfer at charged interfaces play key roles in various industrial and environmental processes. Molecular scale details of ion-ion, ion-water, and ion-surface interactions and their dependence on the character of the ion (ion-specific effects) are still debated. Complex ions, such as SCN- and SeCN-, are particularly interesting due to their unexpected adsorption trends which are ascribed to their permanent dipole moment and non-spherical shape. Here, we combine vibrational sum frequency generation (VSFG) spectroscopy and surface sensitive synchrotron X-ray studies to provide a detailed description of SeCN- adsorption at a charged surfactant monolayer at the air/aqueous interface. The results show that the increasing chemical potential may lead to further reorganization of the adsorbed ions, even though the total interfacial ion population does not change.

Keywords

Liquid-liquid extraction
Sum frequency generation spectroscopy
selenocyanate
X-ray reflectivity
X-ray fluorescence near total reflection
Langmuir monolayer

Supplementary materials

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Supporting Information
Description
Fit parameters of CN and OH stretch region of VSFG spectra, and XR measurements; XFNTR plot at 25 mM KSeCN bulk concentration in absence of DPTAP monolayer; GID results, and CH stretch region of DPTAP monolayer under SSP polarization in presence of different KSeCN concentration.
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