Abstract

The sluggish and inefficient oxygen reduction reaction (ORR) of cathode catalysts in microbial fuel cells is widely accepted as the key restriction in implementing their large-scale actual production application. Recently, modification of nitrogen-doping carbon materials with some transition metal species (M-N-C) is expected to be reserve force to substitute commercial noble metal catalysts. However, long-term stability is always unable to solve effectively. We report a simple synthetic approach of metal-organic framework-derived hollow core-shell Co-nitrogen codoping-modified porous carbon catalysts (N-C@Co/N-C-n%Ni), which is introduced by bits of Ni substance, via the template method and vacuum-assisted impregnation method that exhibit similar catalytic activity to commercial Pt/C catalysts. The hollow core-shell H-N-C@Co/N-C-3%Ni catalyst shows excellent ORR performance and stability, which is 96.31% of the initial current after 125 h continuous reaction, and has been capable of yielding a maximum power density of 1.17 ± 0.01 W·m-2 with 2% decrease in 45 days for long-term continuous operation.

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