4.6 Article

Effects of La2O3 on the Mixed Higher Alcohols Synthesis from Syngas over Co Catalysts: A Combined Theoretical and Experimental Study

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 115, Issue 35, Pages 17440-17451

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp204003q

Keywords

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Funding

  1. U.S. Department of Energy Office of Energy Efficiency and Renewable Energy
  2. W. R Wiley Environmental Molecular Science Laboratory
  3. Department of Energy's Office of Biological and Environmental Research located at Pacific Northwest National Laboratory (PNNL)
  4. Battelle Memorial Institute [DE-AC05-76RLO 1830]

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The promoting role of lanthanum oxide (La2O3) in the catalytic synthesis of mixed higher (C-2-C-6) alcohols from syngas on Co-based catalysts was investigated using a combination of in situ and ex situ X-ray diffraction (XRD), photoelectron spectroscopy (XPS), catalyst reactivity performance studies, and ab initio molecular dynamics (AIMD) simulations. XRD measurements show that doping with La (0.5 wt %) onto activated carbon (AC) supported Co catalyst enhances the Co2C phase formation, whereas the Co2C phase formation is largely suppressed on alumina supported Co catalyst. A strong correlation of the selectivity toward alcohols with the ratio of Co2C/Co particles present in the catalysts was observed. AMID simulations suggest that on AC supports La exists as an oxide phase in the form of small dusters in the vicinity of Co particles. It was found that Co2C formation is energetically favorable, especially for smaller Co particles because of the formation of surface carbide. Theoretical mechanistic studies indicate that oxygenated hydrocarbons can be formed on these catalysts by multiple routes involving the formation of CHxO and CHxCO species at the interface between the La2O3 phase and Co/Co2C. A detailed comparison with previous findings in the literature as well as discussion of the implications of these results upon the improvement of the selectivity of these catalysts toward higher alcohols is presented.

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