Pyridinic and Pyrrolic-N induced carbon nanotubes support bimetallic oxide nanoparticles as high-performance electrocatalysts for oxygen reduction reaction

In-expensive MnO2-based nanostructure has been considered the ideal electrode material for oxygen reduction reaction (ORR) in fuel cell technology. Regardless of their highly active ORR performance, the fuel cross-over capacity and stability of MnO2-based catalysts are still far from satisfying. Herein, we report the highly active SnO2 nanoparticles (NPs) integrated on N-induced carbon nanotube (SnO2@NC) are combined with MnO2 nanoparticles through the electrodeposition to form effective nanostructured in which the MnO2 NPs and SnO2@NC in situ grown on a glassy carbon electrode (MnO2/SnO2@NC) with well-controlled reaction parameters, that exhibits superior ORR activity for the first time. We assessed the marginal role of pyridinic-N and pyrrolic-N in the electrocatalytic ORR activity, synthesis of MnO2/SnO2 bimetallic oxide electrocatalysts, and distribution behavior of NPs. Bimetallic MnO2/SnO2@NC electrode has unique synergistic interactions between MnO2/SnO2 NPs and NC support, which increases electro-active sites, and fast charge transfers towards ORR as compared to other as-prepared electrodes on account of the rational design of the electrode-electrolyte interface plays a significant role in expediting the ORR kinetics. Additionally, the surface nanostructure features, crystalline structure, as well as electronic chemical states of the MnO2/SnO2 NPs embedded in N-induced CNTs, were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Furthermore, bimetallic MnO2/ SnO2@NC nanostructure leads an outstanding ORR performance in the 0.1 M KOH electrolyte, delivering a halfwave potential (-0.878 V) and remarkable limiting current density (-4.14 mA cm-2) and much better tolerance to the ethanol cross-over effect with high stability. Thus, the present strategy opens a new path to the design of a pyridinic-N and pyrrolic-N-oriented bimetallic oxide nanostructure as a high-active electrocatalyst for ORR application.