Enhanced catalytic activity in strained chemically exfoliated WS2 nanosheets for hydrogen evolution
Efficient evolution of hydrogen through electrocatalysis at low overpotentials holds tremendous promise for clean energy. Hydrogen evolution can be easily achieved by electrolysis at large potentials that can be lowered with expensive platinum-based catalysts. Replacement of Pt with inexpensive, ear...
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Veröffentlicht in: | Nature materials 2013-09, Vol.12 (9), p.850-855 |
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Sprache: | eng |
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Zusammenfassung: | Efficient evolution of hydrogen through electrocatalysis at low overpotentials holds tremendous promise for clean energy. Hydrogen evolution can be easily achieved by electrolysis at large potentials that can be lowered with expensive platinum-based catalysts. Replacement of Pt with inexpensive, earth-abundant electrocatalysts would be significantly beneficial for clean and efficient hydrogen evolution. To this end, promising results have been reported using 2H (trigonal prismatic) XS
2
(where X = Mo or W) nanoparticles with a high concentration of metallic edges. The key challenges for XS
2
are increasing the number and catalytic activity of active sites. Here we report monolayered nanosheets of chemically exfoliated WS
2
as efficient catalysts for hydrogen evolution with very low overpotentials. Analyses indicate that the enhanced electrocatalytic activity of WS
2
is associated with the high concentration of the strained metallic 1T (octahedral) phase in the as-exfoliated nanosheets. Our results suggest that chemically exfoliated WS
2
nanosheets are interesting catalysts for hydrogen evolution.
Efficient evolution of hydrogen via electrocatalysis at low overpotentials is promising for clean energy production. Monolayered nanosheets of chemically exfoliated WS
2
are shown to be efficient catalysts for hydrogen evolution at very low overpotentials. The enhanced catalytic performance is associated with the high concentration of the strained metallic octahedral phase in the exfoliated nanosheets. |
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ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/nmat3700 |