The poor kinetics of oxygen reduction reaction (ORR) invites a quest for the development of low-cost and efficient non-Pt electrocatalysts for fuel cells. Herein, a nanocomposite (g-[Co
2N
8]) was synthesized by coordination assembly of CoN
4 macrocyclic moieties on graphene surface. The CoN
4 macrocyclic complex was characterized by UV–Vis, FT-IR, Mass,
1H NMR and
13C NMR spectral studies, whereas UV–Vis, FT-IR, and Mass spectral, Raman, XRD and TEM studies were utilized to characterize the nanocomposite g-[Co
2N
8]. The results suggested that [CoN
4] units are present in self-assembled [Co
2N
8] species. Further, the nanocomposite g-[Co
2N
8] was examined for ORR activity by employing cyclic and linear sweep voltammetry and found that the formal potential (
E1/2) of g-[Co
2N
8] (+0.90 V) was more positive than 20% Pt/C (+0.86 V), indicating a remarkable ORR performance of g-[Co
2N
8] in comparison to 20% Pt/C, followed by 4e-mechanism. Moreover, the nanocomposite (g-[Co
2N
8]) displayed better ORR activity in comparison to [CoN
4] complex which can be attributed to the synergistic incorporation of endo and exo N
4–Co
2+ moieties in the [Co
2N
8] species. In addition, g-[Co
2N
8] electrocatalyst exhibited a comparable stability to 20% Pt/C catalyst after 5000 cycles. This work will help to design multi-metallic coordination polymers with similar or different metal ions in N
4-arrangement for various energy related electrocatalysis.
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