Activating earth-abundant electrocatalysts for efficient, low-cost hydrogen evolution/oxidation: sub-monolayer platinum coatings on titanium tungsten carbide nanoparticles

Most earth-abundant electrocatalysts suffer from negligible activity for the hydrogen oxidation reaction (HOR) and significant overpotentials for the hydrogen evolution reaction (HER) in acidic media. We designed earth-abundant, carbon-supported titanium tungsten carbide (Ti x W 1− x C) nanoparticle...

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Veröffentlicht in:Energy & environmental science 2016-10, Vol.9 (1), p.329-331
Hauptverfasser: Hunt, Sean T, Milina, Maria, Wang, Zhenshu, Román-Leshkov, Yuriy
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Sprache:eng
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Zusammenfassung:Most earth-abundant electrocatalysts suffer from negligible activity for the hydrogen oxidation reaction (HOR) and significant overpotentials for the hydrogen evolution reaction (HER) in acidic media. We designed earth-abundant, carbon-supported titanium tungsten carbide (Ti x W 1− x C) nanoparticles decorated with surface Pt coatings ranging from the "single-atom" to the two-monolayer regime. Reactivity studies demonstrated that sub-monolayer Pt coverages are optimal and could activate the exposed metal carbide sites for both HER and HOR at low overpotentials. Specifically, a 0.25 monolayer coverage of Pt improved the exchange current density of Ti 0.2 W 0.8 C by more than three orders of magnitude. This catalyst outperformed traditional Pt/C by a factor of 13 on a Pt mass basis, allowing for over a 96% reduction in Pt loadings. Deactivation was not observed after 10 000 cycles between −50 and +600 mV vs. RHE in 1.0 M HClO 4 , and activity was maintained after 140 000 catalytic turnovers. A technoeconomic analysis revealed that over the catalyst lifetime, this new architecture could reduce materials and energy costs by a factor of 6 compared to state-of-the-art earth-abundant catalysts and a factor of 12 compared to Pt/C. Decorating titanium tungsten carbide nanoparticles with sub-monolayer platinum surface coatings yields efficient and stable catalysts for hydrogen evolution/oxidation reactions in acidic media.
ISSN:1754-5692
1754-5706
DOI:10.1039/c6ee01929c