The results obtained for binder-free electrodes made of carbon monoliths with narrow micropore size distributions confirm that the specific capacitance in the electrolyte (C2H5)4NBF4/acetonitrile does not depend significantly on the micropore size and support the foregoing constant result of 0.094 ± 0.011 F m(-2).

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Specific capacitance of carbons in aqueous KOH electrolyte seems to have two contributions, a double-layer capacitance and a pseudocapacitance. Moreover, the specific capacitance increases as the specific surface area does. Here, we report that the pseudocapacitance is associated with the K + ion and the double-layer capacitance with both K + and OH − ions. The former ion dominates the capacitance of a real two-electrode supercapacitor. Two microporous carbon monoliths with surface areas similar for micropores below 0.63 nm but different for larger micropores are chosen. There is a correlation between the double-layer capacitance due to those ions and the surface areas due to micropores with sizes above a certain value. It provides information on the size of those ions as they are electroadsorbed at the double layer. The dielectric permittivity associated with the K + and OH − ion is discussed in relation to the confinement of these electroadsorbed ions in the micropores.

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In the present study, a comparative human toxicity assessment between newly developed Mn3O4 nanoparticles with enhanced electrochemical properties (GNA35) and their precursor material (Mn3O4) was performed, employing different in vitro cellular models representing main exposure routes (inhalation, intestinal and dermal contact), namely the human alveolar carcinoma epithelial cell line (A549), the human colorectal adenocarcinoma cell line (HT29), and the reconstructed 3D human epidermal model EpiDerm. The obtained results showed that Mn3O4 and GNA35 harbour similar morphological characteristics, whereas differences were observed in relation to their surface area and electrochemical properties. In regard to their toxicological properties, both nanomaterials induced ROS in the A549 and HT29 cell lines, while cell viability reduction was only observed in the A549 cells. Concerning their skin irritation potential, the studied nanomaterials did not cause a reduction of the skin tissue viability in the test conditions nor interleukin 1 alpha (IL- 1 α) release. Therefore, they can be considered as not irritant nanomaterials according to EU and Globally Harmonized System of Classification and Labelling Chemicals. Our findings provide new insights about the potential harmful effects of Mn3O4 nanomaterials with different properties, demonstrating that the hazard assessment using different human in vitro models is a critical aspect to increase the knowledge on their potential impact upon different exposure routes.