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
Hauptverfasser: Song, Fu‐Zhan, Zhu, Qi‐Long, Yang, Xinchun, Zhan, Wen‐Wen, Pachfule, Pradip, Tsumori, Nobuko, Xu, Qiang
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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.
ISSN:1614-6832
1614-6840
DOI:10.1002/aenm.201701416