In this recent decade, great interest has risen to develop metal-free and cheap, biomass-derived electrocatalysts for oxygen reduction reaction (ORR). Herein, we report a facile strategy to synthesize an electrochemically active nanocarbon material from the renewable and biological resource, wood biomass. The ORR activity of the catalyst material was investigated in 0.1 M KOH solution by employing the rotating disc electrode method. Scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy were employed to obtain more information about the catalyst material’s morphology and composition. The material exhibits outstanding electrocatalytic activity with low onset potential and high current density, similar to that of a commercial Pt/C catalyst in an alkaline medium. The results clearly ascertain that wooden biomass can be easily transformed into novel carbon nanostructures with superior ORR activity and possibility to be used in fuel cells and metal–air batteries.

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Nitrogen-and sulfur-codoped carbon catalysts were prepared as electrocatalytic materials for the oxygen reduction reaction (ORR). Herein, we propose a novel and effective one-pot synthetic approach to prepare a NS-doped carbon catalyst by using the mixture of graphene oxide and multi-walled carbon nanotubes as a carbon support. Successful NS-doping of carbon and formation of the catalytically active sites were confirmed by X-ray photoelectron spectroscopy and with energy dispersion spectroscopy. The ORR activity of NS-codoped carbon was investigated by using a rotating disc electrode method. The NS-doped carbon shows superior ORR performance in alkaline media, and the electrocatalytic mechanism for the reduction of oxygen was well explained by density functional theory calculations of graphene sheets.

Manganese phthalocyanine (MnPc) and copper phthalocyanine (CuPc)-modified electrodes were prepared using multi-walled carbon nanotubes (MWCNTs) as a support material. The catalyst materials were heat treated at four different temperatures to investigate the effect of pyrolysis on the oxygen reduction reaction (ORR) activity of these electrocatalysts. The MWCNT to metal phthalocyanine ratio was varied. Scanning electron microscopy (SEM) was employed to visualise the surface morphology of the electrodes and the x-ray photoelectron spectroscopic (XPS) study was carried out to analyse the surface composition of the most active catalyst materials. The ORR was studied in 0.1 M KOH solution employing the rotating disk electrode (RDE) method. Glassy carbon (GC) electrodes were modified with carbon nanotube-supported metal phthalocyanine catalysts using Tokuyama AS-4 ionomer. The RDE results revealed that the highest electrocatalytic activity for ORR was achieved upon heat treatment at 800°C. CuPc-derived catalyst demonstrated lower catalytic activity as compared to the MnPc-derived counterpart, which is in good agreement with previous literature, whereas the activity of MnPc-based catalyst was higher than that reported earlier.