TY - JOUR
T1 - Electric-double-layer potential distribution in multiple-layer immiscible electrolytes
AU - Das, Siddhartha
AU - Hardt, Steffen
PY - 2011
Y1 - 2011
N2 - In this Brief Report, we calculate the electric-double-layer (EDL) electrostatic potential in a system of several layers of immiscible electrolytes. Verwey-Niessen theory predicts that at the interface between two immiscible electrolytes back-to-back EDLs are formed. The present analysis extends this idea to the case where the immiscible liquids are contained inside a domain with given electrostatic potentials at its boundaries, where the thickness of the individual liquid layer can be comparable to the EDL thickness. Such a system gives rise to a situation where the overall EDL electrostatic potential in the system is dictated by the competitive influences of the boundary-induced effects and the effects induced by the jump in the ion-solvent interaction potential at the liquid-liquid interfaces. Invoking Debye-Hückel linearization, we derive an analytical result for the EDL electrostatic potential for two immiscible electrolyte layers, and extend it for a general system of N such immiscible electrolyte layers. We demonstrate that, depending upon the nature of the interfacial ion-solvent interaction potential jump, the overall EDL potential may manifest a strong influence of the boundary conditions or may invert the influence of the boundary conditions. Effects such as a variation of the ratio of the permittivity or the thickness of the liquids also dictate the overall potential profiles
AB - In this Brief Report, we calculate the electric-double-layer (EDL) electrostatic potential in a system of several layers of immiscible electrolytes. Verwey-Niessen theory predicts that at the interface between two immiscible electrolytes back-to-back EDLs are formed. The present analysis extends this idea to the case where the immiscible liquids are contained inside a domain with given electrostatic potentials at its boundaries, where the thickness of the individual liquid layer can be comparable to the EDL thickness. Such a system gives rise to a situation where the overall EDL electrostatic potential in the system is dictated by the competitive influences of the boundary-induced effects and the effects induced by the jump in the ion-solvent interaction potential at the liquid-liquid interfaces. Invoking Debye-Hückel linearization, we derive an analytical result for the EDL electrostatic potential for two immiscible electrolyte layers, and extend it for a general system of N such immiscible electrolyte layers. We demonstrate that, depending upon the nature of the interfacial ion-solvent interaction potential jump, the overall EDL potential may manifest a strong influence of the boundary conditions or may invert the influence of the boundary conditions. Effects such as a variation of the ratio of the permittivity or the thickness of the liquids also dictate the overall potential profiles
KW - IR-78897
KW - METIS-278500
U2 - 10.1103/PhysRevE.84.022502
DO - 10.1103/PhysRevE.84.022502
M3 - Article
VL - 84
JO - Physical review E: covering statistical, nonlinear, biological, and soft matter physics
JF - Physical review E: covering statistical, nonlinear, biological, and soft matter physics
SN - 2470-0045
IS - 2
M1 - 022502
ER -