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The electrical double layer on gold probed by electrokinetic and surface force measurements
Marcel Giesbers1, J Mieke Kleijn, Martien A Cohen Stuart
1Laboratory of Physical Chemistry and Colloid Science, Wageningen University, PO Box 8038, Wageningen, 6700 EK, The Netherlands.
This study characterizes gold surfaces in aqueous solutions using streaming potential and atomic force microscopy. Results show electric double-layer interactions dominate, with potential influenced by pH and surface oxides.
Area of Science:
- Surface science
- Electrochemistry
- Colloid science
Background:
- Gold surfaces are crucial in catalysis and electronics.
- Understanding gold's electrical double layer in solution is key for controlling surface interactions.
- Previous studies often lack direct force measurements combined with electrokinetic potentials.
Purpose of the Study:
- To characterize the electrical double layer potential of gold surfaces in aqueous solutions.
- To compare results from streaming potential and atomic force microscopy (AFM) force measurements.
- To investigate the influence of pH on the gold/electrolyte interface.
Main Methods:
- Vacuum deposition of thin gold films on glass and silica substrates.
- Streaming potential measurements to determine zeta-potential.
- Colloidal-probe AFM force measurements using gold-coated silica particles.
- Analysis using Derjaguin-Landau-Verwey-Overbeek (DLVO) theory and nonlinear Poisson-Boltzmann equation.
Main Results:
- Streaming potential measurements yielded the zeta-potential of the gold surface.
- AFM force measurements provided the diffuse double-layer potential (ψd).
- Interactions were dominated by electric double-layer overlap; Van der Waals forces were negligible.
- The double-layer potential showed strong pH dependence, attributed to surface oxide species.
- Excellent agreement was found between streaming potential and AFM force measurements.
Conclusions:
- The electrical double layer potential of gold surfaces is accurately determined by combining streaming potential and AFM force measurements.
- Surface oxide species significantly influence the gold/electrolyte interface, particularly its pH dependence.
- This foundational understanding is vital for predicting and controlling adsorption behavior at polarized gold interfaces.
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