Abstract
We evaluated the activities of well-defined Ru@Pt core-shell nanocatalysts for hydrogen evolution and oxidation reactions (HER-HOR) using hanging strips of gas diffusion electrode (GDE) in solution cells. With gas transport limitation alleviated by micro-porous channels in the GDEs, the charge transfer resistances (CTRs) at the hydrogen reversible potential were conveniently determined from linear fit of ohmic-loss-corrected polarization curves. In 1 M HClO 4 at 23 °C, a CTR as low as 0.04 Ω cm -2 was obtained with only 20 μg cm -2 Pt and 11 μg cm -2 Ru using the carbon-supported Ru@Pt with 1:1 Ru:Pt atomic ratio. Derived from temperature-dependent CTRs, the activation barrier of the Ru@Pt catalyst for the HER-HOR in acids is 0.2 eV or 19 kJ mol -1. Using the Ru@Pt catalyst with total metal loadings <50 μg cm -2 for the HER in proton-exchange-membrane water electrolyzers, we recorded uncompromised activity and durability compared to the baseline established with 3 mg cm -2 Pt black.
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CITATION STYLE
Wang, J. X., Zhang, Y., Capuano, C. B., & Ayers, K. E. (2015). Ultralow charge-transfer resistance with ultralow Pt loading for hydrogen evolution and oxidation using Ru@Pt core-shell nanocatalysts. Scientific Reports, 5. https://doi.org/10.1038/srep12220
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