In this study, the refined double layer model of platinum electrodes accounts for chemisorbed oxygen species, oriented interfacial water molecules and ion size effects in solution. It results in a non-monotonic surface charging relation and a peculiar capacitance vs. potential curve with a maximum and maybe negative-defined values in the potential regime of oxide-formation.  
The concepts of total and free charge of platinum single crystal electrodes are revised in this pape...
\u3cp\u3eThe distribution of electric fields within the electrochemical double layer depends on both...
In this work, we theoretically study the differential capacitance of an aqueous electrolyte in conta...
Metal-oxide surfaces act as both Br{\o}nsted acids and bases, which allows the exchange of protons w...
The behavior of the electrical double layer (DL) is known to be different at polarizable interfaces,...
The mass and charge distribution at electrochemical interfaces plays a key role in driving electroch...
It is demonstrated for two cases of apparently ideal, ideally polarizable electrochemical interfaces...
The electrical double-layer plays a key role in important interfacial electrochemical processes from...
We apply a modified Poisson-Boltzmann theory which permits ions of different sizes and excess polari...
We present detailed measurements of the double-layer capacitance of the Pt(111)–electrolyte interfac...
Interfacial charge has a decisive influence on the reactivity of the most common electrochemical rea...
The electric double layer, which is of practical importance, is described. Two theories that yield a...
The properties of the electrical double layer at the interface between oxides and aqueous electrolyt...
The physical origin of charged interfaces involving electrolyte solutions is in the thermodynamic eq...
Electrocatalytic activity is influenced by the surface charge on the solid catalyst. Conventionally,...
The concepts of total and free charge of platinum single crystal electrodes are revised in this pape...
\u3cp\u3eThe distribution of electric fields within the electrochemical double layer depends on both...
In this work, we theoretically study the differential capacitance of an aqueous electrolyte in conta...
Metal-oxide surfaces act as both Br{\o}nsted acids and bases, which allows the exchange of protons w...
The behavior of the electrical double layer (DL) is known to be different at polarizable interfaces,...
The mass and charge distribution at electrochemical interfaces plays a key role in driving electroch...
It is demonstrated for two cases of apparently ideal, ideally polarizable electrochemical interfaces...
The electrical double-layer plays a key role in important interfacial electrochemical processes from...
We apply a modified Poisson-Boltzmann theory which permits ions of different sizes and excess polari...
We present detailed measurements of the double-layer capacitance of the Pt(111)–electrolyte interfac...
Interfacial charge has a decisive influence on the reactivity of the most common electrochemical rea...
The electric double layer, which is of practical importance, is described. Two theories that yield a...
The properties of the electrical double layer at the interface between oxides and aqueous electrolyt...
The physical origin of charged interfaces involving electrolyte solutions is in the thermodynamic eq...
Electrocatalytic activity is influenced by the surface charge on the solid catalyst. Conventionally,...
The concepts of total and free charge of platinum single crystal electrodes are revised in this pape...
\u3cp\u3eThe distribution of electric fields within the electrochemical double layer depends on both...
In this work, we theoretically study the differential capacitance of an aqueous electrolyte in conta...