Metal–Organic Framework Templated Porous Carbon‐Metal Oxide/Reduced Graphene Oxide as Superior Support of Bimetallic Nanoparticles for Efficient Hydrogen Generation from Formic Acid
Ultrafine PdAg nanoparticles (NPs) are successfully immobilized on zirconia/porous carbon/reduced graphene oxide (ZrO2/C/rGO) nanocomposite derived from metal organic framework/graphene oxide. Monodispersed PdAg NPs (diameter ≤2.5 nm) can be facilely anchored on the ZrO2/C/rGO and the aggregation of...
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Veröffentlicht in: | Advanced energy materials 2018-01, Vol.8 (1), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Ultrafine PdAg nanoparticles (NPs) are successfully immobilized on zirconia/porous carbon/reduced graphene oxide (ZrO2/C/rGO) nanocomposite derived from metal organic framework/graphene oxide. Monodispersed PdAg NPs (diameter ≤2.5 nm) can be facilely anchored on the ZrO2/C/rGO and the aggregation of metal NPs can be avoided utmostly. By virtue of the synergistic effect between metal NPs and support, the resulting PdAg@ZrO2/C/rGO exhibits excellent activity (turnover frequency, 4500 h−1 at 333 K) for the dehydrogenation of formic acid. As an effective strategy, it provides an opportunity to immobilize ultrafine metal NPs on metal oxide/porous carbon/reduced graphene oxide, which has tremendous application prospects in various catalytic fields.
A superior support, namely ZrO2/C/rGO derived from metal–organic framework/graphene oxide, to immobilize ultrafine PdAg nanoparticles (NPs) (diameter ≤ 2.5 nm) is reported. By virtue of the synergistic effect between metal NPs and support, the resulting PdAg@ZrO2/C/rGO nanocatalyst shows extremely high catalytic performance (turnover frequency, 4500 h−1) for the dehydrogenation of formic acid. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.201701416 |