Electrogenerated hydrophilic carbon nanomaterials with tailored electrocatalytic activity

This work investigates the influence of the type of buffer electrolyte used in the generation of Electrochemical Hydrophilic Carbon (EHC) on their physical-chemical properties and electrocatalytic activity. The EHC nanomaterials were prepared in three different biological buffers, phosphate, glycine and citrate buffers (EHC@phosphate, EHC@glycine, EHC@citrate) and their surface properties were fully characterized by AFM, XPS and Raman. The EHC nanomaterials drop cast onto a glassy carbon electrode were electrochemically characterized in [Fe(CN)6]3-/4- and [Ru(NH3)6]3+/2+ redox probes solutions, and their electrocatalytic activity was investigated towards hydrogen peroxide and oxygen reduction reactions (ORR) in a phosphate buffer solution. It was found that the nature of buffer electrolyte strongly influences the surface chemical state of the EHC materials, disorder degree in the hexagonal sp2 carbon network and oxygen functional groups, affecting both the EHC electrocatalytic activity towards the ORR and H2O2 reduction reaction. The most catalytic material for the ORR was EHC@citrate, whereas EHC@glycine showed the highest oxygen conversion (n ≅ 2.7 to 3). Moreover, it was shown that the content of oxygen singly bonded to carbon correlates strongly with the number of electrons transferred. A very singular behaviour in the electrochemical reduction of hydrogen peroxide was observed on EHC@glycine, qualitatively interpreted as an autocatalytic reaction. In contrast, a blocking-like effect was depicted on EHC@phosphate. These results must have an important impact in the development of materials with peroxidase-like activity and in the design of O2 sensors with non-sensitivity to H2O2.publishe

Electrochemical properties of oxygen-enriched carbon-based nanomaterials

The introduction of oxygen moieties on a carbon-based material to enhance the electrode material activity for the oxygen reduction reaction (ORR) is a most unexplored experimental approach due to the risk of reducing the electron-transport ability of the electrode material. Herein, it is shown that carbon nanomaterials generated electrochemically from graphite can simultaneously show an anomalous high content of oxygen functionalities and a high heterogeneous electron transfer rate. This study was demonstrated with a set of four samples, prepared at different galvanostatic conditions. All the samples display a non-ordered carbon network dominated by aromatic rings, an O/C ratio greater than 0.4, but different amounts of various oxygen-containing functionalities. The electron-transport properties of the obtained films were appraised by cyclic voltammetry and electrochemical impedance spectroscopy. The application of these metal-free electrode materials to the ORR in the alkaline medium has shown a direct correlation between the materials catalytic activity (potential onset, kinetic current and number of electrons transferred) and the Cdouble bondO amount, whereas a negative correlation was found for Csingle bondO. Their excellent ability for the H2O2 reduction was also demonstrated. This work opens a new perspective on the use of highly oxidized carbon nanomaterials in electrocatalysis.publishe