Hydrogen-Assisted Dissociation of N<sub>2</sub>: Prevalence and Consequences for Ammonia Synthesis on Supported Ru Catalysts
Yukun Bai, Yuanbao Zhang, Jianhua Hu, Li Jiang, Shaolong Wan, Jingdong Lin, Yong Wang, Shuai Wang
Abstract
Understanding the roles of coadsorbates on crowded catalytic surfaces is critical to optimizing industrial catalysts that are generally employed under high-pressure conditions. For ammonia synthesis from N 2 hydrogenation (i.e., the Haber–Bosch process), it is well-known that supported Ru catalysts tend to be highly covered by atomic H species, while the impact of these H species on N 2 activation is still under controversy. Herein, kinetic assessment, isotopic labeling experiments, and in situ spectroscopic characterization were combined to investigate the mechanism of ammonia synthesis on Ru/CeO 2 catalysts with their structure tuned via thermal treatments. Our experimental approaches reveal that the dominant H* surface species limit the availability of vacant Ru sites for the widely proposed direct N 2 dissociation route but instead lead to the prevalence of the H-assisted N 2 dissociation route with the N–N cleavage in N 2 H* intermediates as a kinetically relevant step. Effects of Ru particle size and Ru–CeO 2 interaction on the catalytic activity were kinetically deconvoluted in accordance with this H-assisted mechanism, unveiling their decisive influences on intrinsic activity and surface coverage, respectively. Driven by these fundamental insights gained from the working conditions, superior ammonia formation rates were achieved for supported Ru catalysts via optimizing Ru particle size and metal–support interaction collaboratively.