4.8 Article

Efficient ammonia synthesis over a Ru/La0.5Ce0.5O1.75 catalyst pre-reduced at high temperature

Journal

CHEMICAL SCIENCE
Volume 9, Issue 8, Pages 2230-2237

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc05343f

Keywords

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Funding

  1. CREST, JST program [JPMJCR1341]
  2. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
  3. Grants-in-Aid for Scientific Research [15H04188] Funding Source: KAKEN

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Ammonia is an important feedstock for producing fertiliser and is also a potential energy carrier. However, the process currently used for ammonia synthesis, the Haber-Bosch process, consumes a huge amount of energy; therefore the development of new catalysts for synthesising ammonia at a high rate under mild conditions (low temperature and low pressure) is necessary. Here, we show that Ru/La0.5Ce0.5O1.75 pre-reduced at an unusually high temperature (650 degrees C) catalysed ammonia synthesis at extremely high rates under mild conditions; specifically, at a reaction temperature of 350 degrees C, the rates were 13.4, 31.3, and 44.4 mmol g(-1) h(-1) at 0.1, 1.0, and 3.0 MPa, respectively. Kinetic analysis revealed that this catalyst is free of hydrogen poisoning under the conditions tested. Electron energy loss spectroscopy combined with O-2 absorption capacity measurements revealed that the reduced catalyst consisted of fine Ru particles (mean diameter < 2.0 nm) that were partially covered with partially reduced La0.5Ce0.5O1.75 and were dispersed on a thermostable support. Furthermore, Fourier transform infrared spectra measured after N-2 addition to the catalyst revealed that N-2 adsorption on Ru atoms that interacted directly with the reduced La0.5Ce0.5O1.75 weakened the N N bond and thus promoted its cleavage, which is the rate-determining step for ammonia synthesis. Our results indicate that high-temperature pre-reduction of this catalyst, which consists of Ru supported on a thermostable composite oxide with a cubic fluorite structure and containing reducible cerium, resulted in the formation of many sites that were highly active for N-2 reduction by hydrogen.

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