Univ ised f olyte e the resul fram a relationship between experimental results and the microscopic structure of interfaces between two immiscible electrolyte solutions (ITIES). taining a hydrophobic salt and an aqueous electrolyte of ITIES depends strongly on the nature of the ions [2,6–11]. Often the capacitance curves show a strong asymmetry as a function of the potential and essential [9–11,14–19]. It has been also shown that a thermally adsorption and ion association at the interface. The theory extends our recent studies [19], which have been focused on the effect of ion penetration into an ‘‘un-friendly medium’ ’ and described this effect within a perturbation approach. Here we overcome limitations of the perturbation approach that al...
The effect of capillary waves on the double layer capacitance of the interface between two immiscibl...
Differential capacitances were measured at Hg/room-temperature ionic liquids (RTILs) interfaces as a...
The adsorption of ions at the interface between two immiscible electrolyte solutions (ITIES) is prim...
We develop a theory of the double layer at electrolyte I electrolyte interfaces with account for the...
Using a box profile approximation for the non-electrostatic surface adsorption potentials of anions ...
Electric double layers are ubiquitous, arising in some form in almost every situation involving an i...
Anions generally associate more favorably with the air-water interface than cations. In addition to ...
The structure and differential capacitance of the diffuse part of the electric double layer at solid...
We construct an analytical model to account for the influence of the subnanometer-wide interfacial l...
Water-in-salts are a new family of electrolytes with very promising electrochemical properties for e...
In this paper we analyze the properties of an interface between two immiscible electrolyte solutions...
Interpretation of electrochemical data generated at the interface between two immiscible electrolyte...
Theories of the metal-electrolyte interface are reviewed with particular attention to the prediction...
A theory, based on a modified Poisson–Boltzmann equation, is presented that allows us to calculate t...
The MPB4 theory is used to calculate the differential capacitance of the interface between LiCl in w...
The effect of capillary waves on the double layer capacitance of the interface between two immiscibl...
Differential capacitances were measured at Hg/room-temperature ionic liquids (RTILs) interfaces as a...
The adsorption of ions at the interface between two immiscible electrolyte solutions (ITIES) is prim...
We develop a theory of the double layer at electrolyte I electrolyte interfaces with account for the...
Using a box profile approximation for the non-electrostatic surface adsorption potentials of anions ...
Electric double layers are ubiquitous, arising in some form in almost every situation involving an i...
Anions generally associate more favorably with the air-water interface than cations. In addition to ...
The structure and differential capacitance of the diffuse part of the electric double layer at solid...
We construct an analytical model to account for the influence of the subnanometer-wide interfacial l...
Water-in-salts are a new family of electrolytes with very promising electrochemical properties for e...
In this paper we analyze the properties of an interface between two immiscible electrolyte solutions...
Interpretation of electrochemical data generated at the interface between two immiscible electrolyte...
Theories of the metal-electrolyte interface are reviewed with particular attention to the prediction...
A theory, based on a modified Poisson–Boltzmann equation, is presented that allows us to calculate t...
The MPB4 theory is used to calculate the differential capacitance of the interface between LiCl in w...
The effect of capillary waves on the double layer capacitance of the interface between two immiscibl...
Differential capacitances were measured at Hg/room-temperature ionic liquids (RTILs) interfaces as a...
The adsorption of ions at the interface between two immiscible electrolyte solutions (ITIES) is prim...