Outer Helmholtz Plane of the Electrical Double Layer Formed at the Solid Electrode-Liquid Interface

ChemPhysChem ◽  
2011 ◽  
Vol 12 (8) ◽  
pp. 1430-1434 ◽  
Author(s):  
Masashi Nakamura ◽  
Narumasa Sato ◽  
Nagahiro Hoshi ◽  
Osami Sakata
2007 ◽  
Vol 62 (3-4) ◽  
pp. 187-190 ◽  
Author(s):  
Andrzej Lewandowski ◽  
Maciej Galiński ◽  
Sebastian R. Krajewski

The differential capacity at the electrode (Pt, Au)/ionic liquid interface of 18 ionic liquids (ILs), was measured applying chronoamperometry. The measurements were done by a two electrode system. The double layer capacity at the Pt/IL and Au/IL interface was 1 - 8 μF/cm2. The capacity, estimated from the impedance measurements, was approximately constant within a potential range of ca. 3 V.


Author(s):  
Sebastien Groh ◽  
Holger-dietrich Sassnick ◽  
Victor Ruiz ◽  
Joachim Dzubiella

The hydroxylation state of an oxide surface is a central property of its solid/liquid interface and its corresponding electrical double layer. This study integrated both a reactive force field (ReaxFF)...


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

Sign in / Sign up

Export Citation Format

Share Document