Abstract

A highly active and stable anode catalyst for direct methanol fuel cells is critical to commercialization. Therefore, we have synthesized a unique Fe-doped catalyst Fe–PtBi2/Bi2O2CO3-NC through the classical hydrothermal method and sodium borohydride reduction. Physical characterizations confirm the existence of Bi2O2CO3 nanosheets and successful loading of PtBi nanocages. It is the alternating layer arrangement of Bi2O2CO3, the bifunctional mechanism of PtBi alloy and the synergistic effect of each component that make the synthesized Fe–PtBi2/Bi2O2CO3-NC possess such remarkable methanol oxidation reaction activity (a mass activity of 9345 mA/mgPt in alkaline electrolyte). Moreover, electrochemical measurements also indicate that 51.7% of the mass activity was retained after 1 h durable operation, which is approximately 4.1 times than that of commercial Pt black. Fe–PtBi2/Bi2O2CO3-NC may be applied as a promising alkaline anode catalyst for direct methanol fuel cells due to its outstanding structure and performance. The specific work provides a reference for designing reliable structures and selection of doping elements to enhance the sluggish kinetics of methanol electrooxidation.

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