Abstract

Dinitrogen activation is known as one of the most challenging subjects in chemistry. A number of well-defined metal complexes, nitrides, and clusters have been studied that show catalysis for dinitrogen activation. However, direct evidence of a complete cleavage of the N≡N triple bond at mild conditions is rather limited to date. Herein, we report a study on the dissociation of N2 on small rhodium clusters assisted by surface plasma radiation. From mass spectrometry observation, a few rhodium nitride clusters with an odd number of nitrogen atoms are produced, such as the Rh3N2m-1+ (m = 1-5) series, indicative of N≡N bond dissociation in the mild plasma atmosphere. Interestingly, Rh3N7+ is identified with outstanding mass abundance among the RhnN2m-1+ products, and its ground-state structure is in the form of Rh3N(N2)3+ by capping a nitrogen atom on the top of Rh3+ plane and hanging three N2 molecules beneath the three Rh atoms respectively, giving rise to a C3v symmetry and excellent stability. We demonstrate the catalysis of such a three-atom rhodium cluster and reveal a dinitrogen activation strategy by thermodynamics- and dynamics- favorable chain reactions of multiple N2 molecules with two rhodium clusters under plasma atmosphere.

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