Highly Effective Ru/BaCeO3 Catalysts on Supports with Strong Basic Sites for Ammonia Synthesis

Abstract BaCeO 3 ‐a and BaCeO 3 ‐b, with strong basic sites, were synthesized by using a co‐precipitation method at different calcination temperatures, and used as supports to evaluate their performance in ammonia synthesis. The ammonia synthesis rate with the 1.25 % Ru/BaCeO 3 ‐a catalyst is 24 mmol g −1 h −1 , which is higher than that of 1.25 % Ru/BaCeO 3 ‐b catalyst (18 mmol g −1 h −1 ) at 3 MPa and 450 °C. Moreover, the performance of the 4 % Cs‐1.25 % Ru/BaCeO 3 ‐a catalyst was further improved to 28 mmol g −1 h −1 , and no sign of deactivation was observed after a reaction time of 120 h. The XPS and H 2 temperature‐programmed reduction analyses indicated that the Ru/BaCeO 3 ‐a catalyst has more oxygen vacancies than the Ru/BaCeO 3 ‐b catalyst. In addition, the average Ru particle size of the Ru/BaCeO 3 ‐a catalyst is closer to 2 nm than the Ru/BaCeO 3 ‐b catalyst, which promotes the generation of B 5 ‐type sites (the active site for N 2 dissociation). The CO 2 temperature‐programmed desorption analysis indicates that BaCeO 3 ‐a has a high basic density, which is beneficial for electron transfer to Ru and further facilitates the dissociation of N≡N bonds.