Surface Dynamics for Creating Highly Active Ru Sites for Ammonia Synthesis: Accumulation of a Low-Crystalline, Oxygen-Deficient Nanofraction

To mitigate global problems related to energy and global warming, it is helpful to develop an ammonia synthesis process using catalysts that are highly active under mild conditions. Here we show that the ammonia synthesis activity per weight of catalyst of Ru/Ba/LaCeO x, prereduced at 700 °C, is the highest among reported oxide-supported Ru catalysts, 52.3 mmol h –1 g cat –1 at 350 °C, 1.0 MPa. The turnover frequency of Ru/Ba/LaCeO x at 350 °C was more than 8 times that of Cs + /Ru/MgO, which is a well-known active catalyst used as a benchmark; furthermore, hydrogen poisoning, a typical drawback for oxide-supported Ru catalysts, was effectively suppressed. Scanning transmission electron microscopy observations with energy dispersive X-ray spectrometry and electron energy loss spectroscopy analysis revealed that a low-crystalline, oxygen-deficient nanofraction including Ba 2+, Ce 3+, and La 3+ had accumulated on the Ru particles. This unique structure was obtained by exploiting the surface dynamics of alkaline earth compounds and thermostable rare earth oxides that contain redox-active atoms during the reduction at an unusually high temperature. The nanofraction showed strong electron-donating ability because of the strong basicity of the included cations, removal of carbonate, and formation of oxygen defect sites that eliminated electron-withdrawing O 2– anions from the interface between the nanofraction and Ru atom. Electrons were therefore effectively donated to antibonding π-orbitals of the N 2 molecules via Ru in contact with the nanofraction, and N≡N triple bond cleavage, which is the rate-determining step for ammonia synthesis, was promoted.