Abstract

The anion exchange membrane fuel cell (AEMFC) represents a promising avenue in clean energy equipment. However, its practical application is limited due to the high cost of Pt-based catalysts. Therefore, it is necessary to develop cheap and efficient non-precious metal catalysts. Here in, we employed a simple one-step thermal strategy to synthesize N-doped porous carbon encapsulated Fe and Ni bimetal catalysts (FeNi-N-C-1-1-Ts, T = 900, 950, 1000, 1050 and 1100 ℃). Among these catalysts, FeNi-N-C-1-1-1000 exhibited the highest half-wave potential of 0.885 V, 5 mV higher than 20 wt% Pt/C (0.880 V). Furthermore, it demonstrated a dominant 4e- reduction pathway, exceptional durability and high resistance to methanol. These excellent performances were attributed to the synergistic effect of FeNi bimetallicaction, increased graphitic content, higher Fe/Ni-N4 content, larger BET surface area and the presence of mesoporous structures. Moreover, FeNi-N-C-1-1-1000 exhibited higher half-wave potential than Ni-N-C-1000 and Fe-N-C-1000 owing to the smaller particle size and larger BET surface area of FeNi-N-C after the doping of Ni into Fe-N-C. Finally, FeNi-N-C-1-1-1000 was employed as the cathode in the AEMFC with a loading of 2.0 mg·cm−2, resulting in the highest peak power density of 545 mW·cm−2, surpassing that of 20 wt% Pt/C (375 mW·cm−2) by 170 mW·cm−2.

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