Co Nanoparticles Encapsulated in N-Doped Carbon Nanosheets: Enhancing Oxygen Reduction Catalysis without Metal-Nitrogen Bonding.

It is known that introducing metal nanoparticles (e.g., Fe and Co) into N-doped carbons can enhance the activity of N-doped carbons toward the oxygen reduction reaction (ORR). However, introducing metals into N-doped carbons inevitably causes the formation of multiple active sites. Thus, it is challenging to identify the active sites and unravel mechanisms responsible for enhanced ORR activity. Herein, by developing a new N-heterocyclic carbene (NHC)-Co complex as the nitrogen- and metal-containing precursor, we report the synthesis of N-doped carbon nanosheets embedded with Co nanoparticles as highly active ORR catalysts without direct metal-nitrogen bonding. Electrochemical measurements and X-ray absorption spectroscopy indicate that the carbon-nitrogen sites surrounding Co nanoparticles are responsible for the observed ORR activity and stability. Density functional theory calculations further reveal that Co nanoparticles could facilitate the protonation of O2 and thus promote the ORR activity. These results provide new prospects in the rational design and synthesis of heteroatom-doped carbon materials as non-precious-metal catalysts for various electrochemical reactions.