4.6 Article

Tailor-designed nanowire-structured iron and nickel oxides on platinum catalyst for formic acid electro-oxidation

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RSC ADVANCES
卷 12, 期 31, 页码 20395-20402

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra03386k

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This investigation focuses on designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst consisting of iron and nickel nanowire oxides sequentially assembled onto a platinum substrate was recommended for formic acid electro-oxidation reaction (FAOR). The catalyst exhibited improved catalytic activity and tolerance against CO poisoning compared to the bare platinum catalyst. An activated FeOx/NiOx/Pt catalyst showed a significantly higher activity and a shift in the onset potential of the FAOR. The presence of nano-FeOx and nano-NiOx enriched the catalyst surface with extra oxygen species, effectively mitigating the CO poisoning and facilitating the kinetics of the FAOR.
This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeOx) and nickel (nano-NiOx) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiOx appeared as fibrillar nanowire bundles (ca. 82 nm and 4.2 mu m average diameter and length, respectively), nano-FeOx was deposited as intersecting nanowires (ca. 74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeOx/NiOx/Pt catalyst exhibited ca. 4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeOx/NiOx/Pt catalyst at -0.5 V vs. Ag/AgCl/KCl (sat.) in 0.2 mol L-1 NaOH, a favorable Fe2+/Fe3+ transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeOx/NiOx/Pt catalyst had an activity 7 times higher than that of bare-Pt with an ca. -122 mV shift in the onset potential of the FAOR. The presence of nano-FeOx and nano-NiOx enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra.

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