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A set-up for simultaneous measurement of second harmonic generation and streaming potential and some test applications

Journal Article · · Journal of Colloid and Interface Science
 [1];  [1];  [2];  [3];  [4];  [1]
  1. Karlsruher Inst. of Technology (KIT), Eggenstein-Leopoldshafen (Germany)
  2. University College, London (United Kingdom); Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)
  3. University College, London (United Kingdom)
  4. Johannes Gutenberg Univ., Mainz (Germany)

We present a measurement cell that allows simultaneous measurement of second harmonic generation (SHG) and streaming potential (SP) at mineral-water interfaces with flat specimen that are suitable for non-linear optical (NLO) studies. The set-up directly yields SHG data for the interface of interest and can also be used to obtain information concerning the influence of flow on NLO signals from that interface. The streaming potential is at present measured against a reference substrate (PTFE). The properties of this inert reference can be independently determined for the same conditions. With the new cell, for the first time the SHG signal and the SP for flat surfaces have been simultaneously measured on the same surface. This can in turn be used to unambiguously relate the two observations for identical solution composition. The SHG test of the cell with a fluorite sample confirmed previously observed differences in NLO signal under flow vs. no flow conditions in sum frequency generation (SFG) investigations. As a second test surface, an inert (“hydrophobic”) OTS covered sapphire-c electrolyte interface was studied to verify the zeta-potential measurements with the new cell. For this system we obtained combined zeta-potential/SHG data in the vicinity of the point of zero charge, which were found to be proportional to each other as expected. Furthermore, on the accessible time scales of the SHG measurements no effects of flow, flow velocity and stopped flow occurred on the interfacial water structure. This insensitivity to flow for the inert surface was corroborated by concomitant molecular dynamics simulations. Finally, the set-up was used for simultaneous measurements of the two properties as a function of pH in automated titrations with an oxidic surface. Different polarization combinations obtained in two separate titrations, yielded clearly different SHG data, while under identical conditions zeta-potentials were exactly reproduced. The polarization combination that is characteristic for dipoles perpendicular to the surface scaled with the zeta-potentials over the pH-range studied, while the other did not. Additionally, the work provides an advanced approach for investigating liquid/surface interactions which play a major role in our environment. Furthermore, the set-up can be upgraded for SFG studies, which will allow more detailed studies on the chemistry and the water structure at a given interface, but also the combined study of specific adsorption including kinetics in combination with electrokinetics. Such investigations are crucial for the basic understanding of many environmental processes from aquatic to atmospheric systems.

Research Organization:
Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)
Sponsoring Organization:
USDOE National Nuclear Security Administration (NNSA); German Research Foundation (DFG); Marie Curie Career Integration Grants
Grant/Contract Number:
AC04-94AL85000; AC02-05CH11231
OSTI ID:
1644077
Alternate ID(s):
OSTI ID: 1543559
OSTI ID: 1592499
Report Number(s):
SAND--2020-7179J; 687350
Journal Information:
Journal of Colloid and Interface Science, Journal Name: Journal of Colloid and Interface Science Vol. 529; ISSN 0021-9797
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English

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