4.8 Article

CO2 hydrogenation on Au/TiC, Cu/TiC, and Ni/TiC catalysts: Production of CO, methanol, and methane

Journal

JOURNAL OF CATALYSIS
Volume 307, Issue -, Pages 162-169

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2013.07.023

Keywords

CO2 activation; CO production; Methane synthesis; Metal carbides; Noble metals

Funding

  1. US Department of Energy, Chemical Sciences Division [DE-AC02-98CH10886]
  2. INTEVEP
  3. IDB
  4. Nippon Foundation for Materials Science
  5. Spanish MICINN/MINECO research grants [FIS2008-02238, CTQ2010-14872/BQU, CTQ2012-30751]
  6. Generalitat de Catalunya grants [2009SGR1041]
  7. XRQTC
  8. ICREA Academia Award for excellence

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Small Au, Cu, and Ni particles in contact with TiC(001) display a very high activity for the catalytic hydrogenation of CO2. The major product over these catalysts is CO which is produced by the reverse water gas shift reaction (RWGS, CO2 + H-2 -> CO + H2O). In the cases of Au/TiC(001) and Cu/TiC(001), a substantial amount of methanol is also produced, but no methane is detected. Ni/TiC(001) produces a mixture of CO, methanol, and methane. The highest catalytic activity is found for small two-dimensional particles or clusters of the admetals in close contact with TiC(001). The catalytic activity of the supported metals can be orders of magnitude higher than those-of Au(100), Cu(100), or Ni(100). Density functional calculations point to HOCO as a key intermediate for the generation of CO through the RWGS, with the production of methanol probably involving the hydrogenation of a HCOO intermediate or the CO generated by the RWGS. (C) 2013 Elsevier Inc. All rights reserved.

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