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Highly-efficient RuNi single-atom alloy catalysts toward chemoselective hydrogenation of nitroarenes.


ABSTRACT: The design and exploitation of high-performance catalysts have gained considerable attention in selective hydrogenation reactions, but remain a huge challenge. Herein, we report a RuNi single atom alloy (SAA) in which Ru single atoms are anchored onto Ni nanoparticle surface via Ru-Ni coordination accompanied with electron transfer from sub-surface Ni to Ru. The optimal catalyst 0.4% RuNi SAA exhibits simultaneously improved activity (TOF value: 4293 h-1) and chemoselectivity toward selective hydrogenation of 4-nitrostyrene to 4-aminostyrene (yield: >99%), which is, to the best of our knowledge, the highest level compared with reported heterogeneous catalysts. In situ experiments and theoretical calculations reveal that the Ru-Ni interfacial sites as intrinsic active centers facilitate the preferential cleavage of N-O bond with a decreased energy barrier by 0.28 eV. In addition, the Ru-Ni synergistic catalysis promotes the formation of intermediates (C8H7NO* and C8H7NOH*) and accelerates the rate-determining step (hydrogenation of C8H7NOH*).

SUBMITTER: Liu W 

PROVIDER: S-EPMC9178046 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Highly-efficient RuNi single-atom alloy catalysts toward chemoselective hydrogenation of nitroarenes.

Liu Wei W   Feng Haisong H   Yang Yusen Y   Niu Yiming Y   Wang Lei L   Yin Pan P   Hong Song S   Zhang Bingsen B   Zhang Xin X   Wei Min M  

Nature communications 20220608 1


The design and exploitation of high-performance catalysts have gained considerable attention in selective hydrogenation reactions, but remain a huge challenge. Herein, we report a RuNi single atom alloy (SAA) in which Ru single atoms are anchored onto Ni nanoparticle surface via Ru-Ni coordination accompanied with electron transfer from sub-surface Ni to Ru. The optimal catalyst 0.4% RuNi SAA exhibits simultaneously improved activity (TOF value: 4293 h<sup>-1</sup>) and chemoselectivity toward s  ...[more]

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