Electrical double layer at the interface between two immiscible electrolyte solutions

1988 ◽  
Vol 88 (4) ◽  
pp. 617-632 ◽  
Author(s):  
Zdenek Samec
Soft Matter ◽  
2011 ◽  
Vol 7 (4) ◽  
pp. 1441-1449 ◽  
Author(s):  
Alberto Martín-Molina ◽  
José Guadalupe Ibarra-Armenta ◽  
Enrique González-Tovar ◽  
Roque Hidalgo-Álvarez ◽  
Manuel Quesada-Pérez

2005 ◽  
Vol 58 (12) ◽  
pp. 837 ◽  
Author(s):  
Robert F. Considine ◽  
Calum J. Drummond ◽  
David R. Dixon

Atomic force microscopy (AFM) has been used to measure the force of interaction between pairs of silica colloids in aqueous inorganic and natural organic electrolyte solutions. In solutions containing a mixture of mono- and divalent inorganic ions, the force measurements on approach can be understood in terms of an electrical double-layer interaction, with decay lengths being comparable to the predicted Debye length. The force of interaction on separation in these mixed electrolyte solutions has been found to be entirely repulsive. Force measurements in a mixture of monovalent ions and natural organic matter (NOM), which is a common component of natural waters, are also reported. The decay length of the electrical double-layer interaction is observed to decrease upon addition of NOM. Force measurements on separation are characterized by pH-dependent adhesion, which has been interpreted in terms of specific surface adsorption and the intermolecular interaction of NOM. A comparison with particle micro-electrophoresis data for the silica colloids in the mixed electrolyte solutions has also been made.


2019 ◽  
Author(s):  
Divya Bohra ◽  
Jehanzeb Chaudhry ◽  
Thomas Burdyny ◽  
Evgeny Pidko ◽  
wilson smith

<p>The environment of a CO<sub>2</sub> electroreduction (CO<sub>2</sub>ER) catalyst is intimately coupled with the surface reaction energetics and is therefore a critical aspect of the overall system performance. The immediate reaction environment of the electrocatalyst constitutes the electrical double layer (EDL) which extends a few nanometers into the electrolyte and screens the surface charge density. In this study, we resolve the species concentrations and potential profiles in the EDL of a CO<sub>2</sub>ER system by self-consistently solving the migration, diffusion and reaction phenomena using the generalized modified Poisson-Nernst-Planck (GMPNP) equations which include the effect of volume exclusion due to the solvated size of solution species. We demonstrate that the concentration of solvated cations builds at the outer Helmholtz plane (OHP) with increasing applied potential until the steric limit is reached. The formation of the EDL is expected to have important consequences for the transport of the CO<sub>2</sub> molecule to the catalyst surface. The electric field in the EDL diminishes the pH in the first 5 nm from the OHP, with an accumulation of protons and a concomitant depletion of hydroxide ions. This is a considerable departure from the results obtained using reaction-diffusion models where migration is ignored. Finally, we use the GMPNP model to compare the nature of the EDL for different alkali metal cations to show the effect of solvated size and polarization of water on the resultant electric field. Our results establish the significance of the EDL and electrostatic forces in defining the local reaction environment of CO<sub>2</sub> electrocatalysts.</p>


2021 ◽  
pp. 138416
Author(s):  
Sofia B. Davey ◽  
Amanda P. Cameron ◽  
Kenneth G. Latham ◽  
Scott W. Donne

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