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 |
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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. |
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ISSN: | 1754-5692 1754-5706 |
DOI: | 10.1039/c6ee01929c |