4.8 Article

Steam-created grain boundaries for methane C-H activation in palladium catalysts

Journal

SCIENCE
Volume 373, Issue 6562, Pages 1518-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abj5291

Keywords

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Funding

  1. Stanford Natural Gas Initiative
  2. US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences [DE-FG0205ER15731]
  3. National Science Foundation [ECCS-1542152, 1956300]
  4. HydroGEN Advanced Water Splitting Consortium, as part of the Energy Materials Network under the US Department of Energy, Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office [DE-EE-0008084]
  5. National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science User Facility at Lawrence Berkeley National Laboratory [DEAC02-05CH11231]
  6. DOE [DE-AC02-06CH11357]
  7. US Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division [DE-AC02-76SF00515]
  8. Direct For Mathematical & Physical Scien
  9. Division Of Chemistry [1956300] Funding Source: National Science Foundation

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The study showed that high-temperature steam pretreatment can enhance the mass-specific reaction rate for carbon-hydrogen (C-H) activation in methane oxidation on palladium catalysts. Experimental and theoretical methods demonstrated that crystal twinning increased grain boundary density, leading to higher reactivity.
Defects may display high reactivity because the specific arrangement of atoms differs from crystalline surfaces. We demonstrate that high-temperature steam pretreatment of palladium catalysts provides a 12-fold increase in the mass-specific reaction rate for carbon-hydrogen (C-H) activation in methane oxidation compared with conventional pretreatments. Through a combination of experimental and theoretical methods, we demonstrate that an increase in the grain boundary density through crystal twinning is achieved during the steam pretreatment and oxidation and is responsible for the increased reactivity. The grain boundaries are highly stable during reaction and show specific rates at least two orders of magnitude higher than other sites on the palladium on alumina (Pd/Al2O3) catalysts. Theoretical calculations show that strain introduced by the defective structure can enhance C-H bond activation. Introduction of grain boundaries through laser ablation led to further rate increases.

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