4.8 Article

Combining in Situ NEXAFS Spectroscopy and CO2 Methanation Kinetics To Study Pt and Co Nanoparticle Catalysts Reveals Key Insights into the Role of Platinum in Promoted Cobalt Catalysis

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 28, Pages 9898-9901

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja505286j

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Funding

  1. Division of Chemical Sciences, Geological and Biosciences of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  3. Total S.A.

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The mechanistic role of platinum and precious metals in promoting cobalt hydrogenation catalysts of the type used in reactions such as Fischer-Tropsch synthesis is highly debated. Here we use well-defined monometallic Pt and Co nanoparticles (NPs) and CO2 methanation as a probe reaction to show that Pt NPs deposited near Co NPs can enhance the CO2 methanation rate by up to a factor of 6 per Co surface atom. In situ NEXAFS spectroscopy of these same Pt NP plus Co NP systems in hydrogen shows that the presence of nearby Pt NPs is able to significantly enhance reduction of the Co at temperatures relevant to Fischer-Tropsch synthesis and CO2 methanation. The mechanistic role of Pt in these reactions is discussed in light of these findings.

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