Electrofabrication of large volume di- and tripeptide hydrogels via hydroquinone oxidation

The fabrication of protected peptide-based hydrogels on electrode surfaces can be achieved by employing the electrochemical oxidation of hydroquinone to benzoquinone, liberating protons at the electrode-solution interface. The localised reduction...

3D Simulation and Artificial Neural Networks Application in the Diffusion Study of Champignon Mushroom/Solution Interface During the Salting

The influence of the film formed during the salting of champignon mushrooms with brine containing NaCl and KCl was modeled using the finite elements method (FEM). It was verified that the film formed on the mushroom surface had a greater influence in the static salting since the diffusion of the ions was 7.5-fold smaller in this system than in the stirred salting. The application of self-organizing maps showed that the ions diffusion along the surface of the solid presented a heterogeneous occurrence and depended on the region for both static and stirred salting. A direct relation was observed among the mushroom surface morphology, the salts diffusion behavior, and the film formation. In addition, the film was not completely extinguished in the stirred system, although it has a minimal influence as the film formation is also dependent on the biosolid surface.

Electrocatalytic Properties of Ni(II) Schiff Base Complex Polymer Films

Platinum electrodes were modified with polymers of the (±)-trans-N,N′-bis(salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn)]) and (±)-trans-N,N′-bis(3,3′-tert-Bu-salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn(Bu))]) complexes to study their electrocatalytic and electroanalytical properties. Poly[Ni(salcn)] and poly[Ni(salcn(Bu))]) modified electrodes catalyze the oxidation of catechol, aspartic acid and NO2−. In the case of poly[Ni(salcn)] modified electrodes, the electrocatalysis process depends on the electroactive surface coverage. The films with low electroactive surface coverage are only a barrier in the path of the reducer to the electrode surface. The films with more electroactive surface coverage ensure both electrocatalysis inside the film and oxidation of the reducer directly on the electrode surface. In the films with the most electroactive surface coverage, electrocatalysis occurs only at the polymer–solution interface. The analysis was based on cyclic voltammetry, EQCM (electrochemical quartz crystal microbalance) and rotating disc electrode method.

Electrochemical Impedance Spectroscopy and Its Applications

Electrochemistry has become an important and recognized field for the future since many of its approaches contemplate the establishment of stable energy supplies and the minimization of our impact on the environment. In this regard, electrochemistry can face both objectives by studying the electrode/solution interface. As a result, different electrochemical techniques can be used to study the interface to understand the electron transfer phenomena in different reactions. Considering this, one of the most useful techniques to understand the electrode/solution interface is electrochemical impedance spectroscopy. This technique allows us to describe the electrode behavior in the presence of a certain electrolyte in terms of electrical parameters such as resistances and capacitances, among others. With this information, we can infer the electrochemical behavior toward a specific reaction and the capacity of the electrode to carry on the electron transfer depending on its resistance (impedance) values. The aim of this chapter is to go from the theory, based on Ohm’s Law and its derivations, to actual applications. This will lead us to characterize the solution, electrode, and the interface between these two phases based on their electrical components by using an equivalent electrical circuit, such as the Randles equivalent circuit.

Double-Layer Capacitances Caused by Ion–Solvent Interaction in the Form of Langmuir-Typed Concentration Dependence

Variations of the double layer capacitances (DLCs) at a platinum electrode with concentrations and kinds of salts in aqueous solutions were examined in the context of facilitating orientation of solvent dipoles. With an increase in ionic concentrations, the DLCs increased by ca. a half and then kept constant at concentrations over 1 mol dm−3. This increase was classically explained in terms of the Gouy–Chapman (GC) equation combined with the Stern model. Unfortunately, measured DLCs were neither satisfied with the Stern model nor the GC theory. Our model suggests that salts destroy hydrogen bonds at the electrode–solution interface to orient water dipoles toward the external electric field. A degree of the orientation depends on the interaction energy between the salt ion and a water dipole. The statistical mechanic calculation allowed us to derive an equation for the DLC as a function of salt concentration and the interaction energy. The equation took the Langmuir-type in the relation with the concentration. The interaction energy was obtained for eight kinds of salts. The energy showed a linear relation with the interaction energy of ion–solvent for viscosity, called the B-coefficient.