Multiple reaction pathway on alkaline earth imide supported catalysts for efficient ammonia synthesis

The tunability of reaction pathways is required for exploring efficient and low cost catalysts for ammonia synthesis. There is an obstacle by the limitations arising from scaling relation for this purpose. Here, we demonstrate that the alkali earth imides (AeNH) combined with transition metal (TM = Fe, Co and Ni) catalysts can overcome this difficulty by utilizing functionalities arising from concerted role of active defects on the support surface and loaded transition metals. These catalysts enable ammonia production through multiple reaction pathways. The reaction rate of Co/SrNH is as high as 1686.7 mmol center dot gCo-1 center dot h-1 and the TOFs reaches above 500 h-1 at 400 degrees C and 0.9 MPa, outperforming other reported Co-based catalysts as well as the benchmark Cs-Ru/MgO catalyst and industrial wustite-based Fe catalyst under the same reaction conditions. Experimental and theoretical results show that the synergistic effect of nitrogen affinity of 3d TMs and in-situ formed NH2- vacancy of alkali earth imides regulate the reaction pathways of the ammonia production, resulting in distinct catalytic performance different from 3d TMs. It was thus demonstrated that the appropriate combination of metal and support is essential for controlling the reaction pathway and realizing highly active and low cost catalysts for ammonia synthesis. The presence of electrically active defects on the surface of the support has been shown to be effective for N2 activation. Here the authors discover that electron-rich polyanionic NH2- defect allows for efficient ammonia synthesis via multiple reaction pathway by incorporating various affordable transition metals.

Automated summary

This study demonstrates the successful synthesis of ammonia through multiple reaction pathways by combining alkali earth imides with transition metal catalysts. The experimental and theoretical results highlight the importance of the combination of metal and support for controlling reaction pathways and achieving highly active and low cost catalysts.