Minimizing
the particle size of transition metals and constructing
heteroatom-co-doped carbon with a high surface area are deemed imperative
in maximizing the atomic utilization of carbon-based materials. Herein,
the atomically dispersed Co sites anchored on interconnected B, N-doped
carbon nanotubes (B, N, Co/C nanotubes) are prepared through facile
molten-salt-assisted pyrolysis of B/N/Co precursors following chemical
etching. The Co single atom is demonstrated to form a Co–N4 planar configuration by XAFS analysis. The developed B, N,
Co/C nanotubes exhibit excellent oxygen reduction reaction (ORR) performance
in alkaline medium. They not only display a positive half-wave potential
(E
1/2, 0.87 V), surpassing that of commercial
Pt/C (0.84 V), but also show an outstanding stability (only 1 mV degrade
can be observed after 10,000 cycles) and a high fuel selectivity.
These excellent ORR performances derive from the efficient synergy
of atomically dispersed Co active sites, unique 3D tubelike assembly
structure, large specific surface area, and high graphitization degree.
Moreover, the B, N, Co/C nanotubes assisted by RuO2 as
an air cathode can enable rechargeable Zn–air batteries with
larger power density (125.0 mW cm–2), higher specific
capacity (746.8 mA h gZn
–1), and better
cycling stability than those of conventional Pt/C + RuO2-based Zn–air batteries.
Pt–Cu TNs can be simply achieved within a few minutes by an H+-assisted disproportionation reaction using Cu2O tetradecahedrons as the template. Due to its unique structural advantages, these Pt–Cu TNs exhibit extraordinary electrocatalytic performance toward MOR.
Hollow PtPdCu trimetallic octahedrons were prepared under mild conditions, exhibiting enhanced activity toward the oxygen reduction reaction in acid media.
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