Entropy Variation in the Two-dimensional Phase Transition of Anthracene Adsorbed at the Hg Electrode/Ethylene Glycol Solution Interface

The adsorption of anthracene (C14H10), at the mercury electrode/ethylene glycol (EG) solution interface, is characterized by a low and almost constant capacity (about 8 μF cm−2) region (capacitive “pit” or “plateau”) in capacity vs. potential curves, upon selection of suitable values of temperature, bulk concentration and applied potential values. This result is rationalized assuming the occurrence of a 2D phase transition between two distinct adsorbed phases: (i) a “disordered” phase, characterized by a flat “parallel” disposition of the aromatic moiety on the electrode surface (ii) an “ordered” phase, characterized by a “perpendicular” disposition of the aromatic moiety on the electrode surface. The experimental evidence is rationalized by considering the chemical potential as an explicit function of the “electric field/adsorbed molecule” interaction. Such a modelistic approach enables the determination of the relevant standard entropy variation

Entropy Variation in the Two-dimensional Phase Transition of Anthracene Adsorbed at the Hg Electrode/Ethylene Glycol Solution Interface

The adsorption of anthracene (C14H10), at the mercury electrode/ethylene glycol (EG) solution interface, is characterized by a low and almost constant capacity (about 8 μF cm−2) region (capacitive “pit” or “plateau”) in capacity vs. potential curves, upon selection of suitable values of temperature, bulk concentration and applied potential values. This result is rationalized assuming the occurrence of a 2D phase transition between two distinct adsorbed phases: (i) a “disordered” phase, characterized by a flat “parallel” disposition of the aromatic moiety on the electrode surface (ii) an “ordered” phase, characterized by a “perpendicular” disposition of the aromatic moiety on the electrode surface. The experimental evidence is rationalized by considering the chemical potential as an explicit function of the “electric field/adsorbed molecule” interaction. Such a modelistic approach enables the determination of the relevant standard entropy variation