Abstract
The efficient reduction of oxygen in fuel cell technology using platinum group metals (PGMs) faces challenges like sluggish kinetics, high costs, and poor durability. To overcome these limitations, PGM-free oxygen reduction reaction (ORR) electrocatalysts are sought after. Transition-metal-based electrocatalysts, specifically metal-nitrogen co-doped carbon (M-N/C, M = Fe, Co, etc.), have emerged as promising alternatives due to their abundant pore structures, high surface area, conductivity, and cost-effectiveness. This review explores various non-precious metal electrocatalysts for ORR, highlighting pyrolyzed transition metal nitrogen-containing complexes on carbon (M–Nx/C) as outstanding candidates, with Fe-N/C demonstrating remarkable performance. In this study, we introduce a novel approach to construct Fe-Nx doped large-diameter carbon nanotubes (Fe,Ni-N/C) by pyrolyzing zeolitic imidazolium frameworks-8 (ZIF-8) functionalized with nickel acetate. This approach capitalizes on strong intercalation between acetate and metal ions, promoting Fe-Nx active site formation while generating large-diameter carbon nanotubes. The resulting catalyst facilitates rapid mass transport and maximizes active site exposure, nearing the performance of Pt/C. Our catalyst exhibits an initial potential of 1.03 V, a half-wave potential of 0.88 V, and a limit current of 5.5 mA cm−2. Remarkably, it retains 85.7% of its initial performance in a 36,000 s chronoamperometry test, demonstrating superior durability and methanol toxicity resistance compared to Pt/C. Large-diameter carbon nanotubes offer a potential alternative electrocatalyst, eliminating the need for templates, simplifying mass production for applications like sensors, supercapacitors, and lithium-ion batteries. Furthermore, our Fe,Ni-N/C catalyst outperforms commercial Pt/C, making it a promising choice for ORR applications in fuel cells.
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