Probing the electro-catalytic ORR activity of cobalt-incorporated nitrogen-doped CNTs

- Co-NCNTs exhibited ORR activity and excellent stability in acid and alkaline medium.
- The excellent durability of Co-NCNTs is due to dense graphite layers' protection.
- Co-Nx species at the arches of Co-NCNTs are mainly responsible for ORR in acid.
- Nitrogen doping of Co-NCNTs mainly contributes to ORR activity in alkaline medium.

Catalysts for oxygen reduction reaction (ORR) are crucial for fuel cells. However, the rarity and poor durability of Pt-based catalysts have prohibited its commercialization. Herein, we report cobalt-incorporated nitrogen-doped CNT (Co-NCNT) as a Pt-free, efficient and low-cost catalyst for ORR, which is synthesized by the pyrolysis of melamine formaldehyde in which cobalt nitrate is homogeneously dispersed. The electro-catalyst exhibits reasonable activity for ORR in both acidic and alkaline media. Moreover, its activity remains almost unchanged in 1000 electrochemical cycles in both acidic and alkaline media due to the protection by dense graphite layers. More specifically, detailed electron energy loss spectroscopy investigations show that the doped nitrogen species tend to co-accumulate with cobalt at the arch areas of carbon nanotubes where catalytically active Co-Nx species are proposed to form. Combined with probe tests upon ligating, Co-Nx species enriched at the arches has found to be mainly responsible for the ORR activity in acidic medium, while in alkaline medium, nitrogen doped carbon species (N-C) of Co-NCNTs are proposed to serve as dominant active sites for ORR. The ratio of Co-Nx site density to N-C site density plays a significant role in determining ORR activity.

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