The current catalytic reaction mechanism for ammonia synthesis relies on either dissociative or associative routes, in which adsorbed N 2 dissociates directly or is hydrogenated step-by-step until it is broken upon the release of NH 3 through associative adsorption. Here, we propose a concerted mechanism of associative and dissociative routes for ammonia synthesis over a cobalt-loaded nitride catalyst. Isotope exchange experiments reveal that the adsorbed N 2 can be activated on both Co metal and the nitride support, which leads to superior low-temperature catalytic performance. The cooperation of the surface low work function (2.6 eV) feature and the formation of surface nitrogen vacancies on the CeN support gives rise to a dual pathway for N 2 activation with much reduced activation energy (45 kJ·mol –1 ) over that of Co-based catalysts reported so far, which results in efficient ammonia synthesis under mild conditions.
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Ye et al. (2021) studied this question.
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