Low-Temperature Synthesis of Perovskite Oxynitride-Hydrides as Ammonia Synthesis Catalysts

Abstract

Mixed anionic materials such as oxyhydrides and oxynitrides have recently attracted significant attention due to their unique properties, such as fast hydride ion conduction, enhanced ferroelectrics, and catalytic activity. However, high temperature (≥800 °C) and/or complicated processes are required for the synthesis of these compounds. Here we report that a novel perovskite oxynitride-hydride, BaCeO 3– x N y H z, can be directly synthesized by the reaction of CeO 2 with Ba(NH 2 ) 2 at low temperatures (300–600 °C). BaCeO 3– x N y H z, with and without transition metal nanoparticles, functions as an efficient catalyst for ammonia synthesis through the lattice N 3– and H – ion-mediated Mars–van Krevelen mechanism, while ammonia synthesis occurs over conventional catalysts through a Langmuir–Hinshelwood mechanism with high energy barriers (85–121 kJ mol –1 ). As a consequence, the unique reaction mechanism leads to enhancement of the activity of BaCeO 3 -based catalysts by a factor of 8–218 and lowers the activation energy (46–62 kJ mol –1 ) for ammonia synthesis. Furthermore, isotopic experiments reveal that this catalyst shifts the rate-determining step for ammonia synthesis from N 2 dissociation to N–H bond formation.