On the electric double-layer structure at carbon electrode/organic electrolyte solution interface analyzed by ac impedance and electrochemical quartz-crystal microbalance responses

2011 ◽  
Vol 56 (21) ◽  
pp. 7319-7326 ◽  
Author(s):  
In-Tae Kim ◽  
Minato Egashira ◽  
Nobuko Yoshimoto ◽  
Masayuki Morita
2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
J. J. López-García ◽  
J. Horno ◽  
C. Grosse

The structure and differential capacitance of the diffuse part of the electric double layer at solid-electrolyte solution interfaces are examined using a theoretical model that takes into account the finite ion size by modeling the solution as a suspension of polarizable insulating spheres in water. This formalism is applied to binary and mixed electrolyte solutions using the “Boublik–Mansoori–Carnahan–Starling–Leland” (BMCSL) theory for the steric interactions among ions. It is shown that the ionic size differences have a strong bearing on the diffuse part of the electric double layer structure, as well as on the differential capacitance dependence on the surface potential for mixed electrolytes.


The Analyst ◽  
2021 ◽  
Author(s):  
Christian Leppin ◽  
Astrid Peschel ◽  
Frederick Sebastian Meyer ◽  
Arne Langhoff ◽  
Diethelm Johannsmann

A fast EQCM measures the kinetics of the viscosity changes inside the double layer following voltage jumps.


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