LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Turning Carbon Atoms into Highly Active Oxygen Reduction Reaction Electrocatalytic Sites in Nitrogen-Doped Graphene-Coated Co@Ag

Photo from wikipedia

In recent years, 3d transition metals or alloys encapsulated by graphene layers (M@NG) have been emerging as prospective electrocatalysts especially for hydrogen evolution reactions (HERs) and oxygen evolution reactions (OERs).… Click to show full abstract

In recent years, 3d transition metals or alloys encapsulated by graphene layers (M@NG) have been emerging as prospective electrocatalysts especially for hydrogen evolution reactions (HERs) and oxygen evolution reactions (OERs). However, this strategy is limited in preparation of high-performance oxygen reduction reaction (ORR) catalysts. Herein we prepared Co@Ag bimetallic nanoparticles embedded in nitrogen-rich graphene layers via pyrolysis metal organic frameworks (MOFs). The catalyst displays extraordinarily high ORR performance with a high onset potential of 0.989 V and a half-wave potential of 0.872 V in 0.1 M KOH. Moreover, it shows a superb long-term stability performance after 5000 cycles on account of the carbon layers that protect the material from corrosion as well as high methyl alcohol tolerance under methanol environments. Density functional theory calculations suggest that carbon atoms, which are adjacent to nitrogen dopants in Co@Ag@NC, are active sites for ORR. Especially, Ag “mantle” in ...

Keywords: carbon atoms; carbon; reduction reaction; oxygen reduction

Journal Title: ACS Sustainable Chemistry & Engineering
Year Published: 2018

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.