4.6 Article

Induced activation of the commercial Cu/ZnO/Al2O3 catalyst for the steam reforming of methanol

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NATURE CATALYSIS
卷 5, 期 2, 页码 99-108

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NATURE PORTFOLIO
DOI: 10.1038/s41929-021-00729-4

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资金

  1. National Natural Science Foundation of China [22078089, 21908054, 22075076]
  2. Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
  3. Shanghai Sailing Program [19YF1410600]
  4. Shanghai Rising-star Program [20QA1402400]
  5. Shanghai Municipal Science and Technology Major Project [2018SHZDZX03]
  6. Fundamental Research Funds for the Central Universities
  7. Programme of Introducing Talents of Discipline to Universities [B16017]
  8. Center for Understanding & Control of Acid Gas-Induced Evolution of Materials for Energy - US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0012577]
  9. Frontiers Science Center for Materiobiology and Dynamic Chemistry
  10. Feringa Nobel Prize Scientist Joint Research Center

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The surface structure of catalysts plays a crucial role in their catalytic performance. This study reveals that manipulating the catalyst surface reconstruction process can enhance long-term stability and catalytic activity by controlling the composition of reducing agents during activation.
The surface structure of heterogeneous catalysts is closely associated with their catalytic performance. Current efforts for structural modification mainly focus on improving the catalyst synthesis details. Here we reveal an induced activation strategy to manipulate the catalyst surface reconstruction process by controlling the composition of reducing agents at the activation stage. Exposing the commercial Cu/ZnO/Al2O3 catalyst to a H-2/H2O/CH3OH/N-2 mixture at 300 degrees C and atmospheric pressure is found to accelerate the migration of ZnOx species onto the surface of metallic Cu-0 nanoparticles via an adsorbate-induced strong metal-support interaction. Such a morphological evolution improves the long-term stability by threefold and results in more abundant Cu-ZnOx interfacial sites with catalytic activity enhanced by twofold towards the methanol steam reforming reaction.

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