Ternary Ruthenium Complex Hydrides for Ammonia Synthesis
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Abstract
Ammonia is the feedstock for nitrogen fertilizers and a potential carbon-free energy carrier, but the current production emits more CO 2 than any other chemical producing reaction in the world. The demand for decarbonizing the ammonia industry by using renewable energy has renewed research interests into catalyst development for effective N 2 reduction under mild conditions, a grand scientific challenge. Conventional heterogeneous catalysts based on metallic Fe or Ru mediate dinitrogen dissociation and hydrogenation through a relatively energy-costing pathway. The ternary ruthenium complex hydrides Li 4 RuH 6 and Ba 2 RuH 6 reported in this work, on the other hand, represent an entirely new class of compound catalysts, which are composed of the electron- and H-rich [RuH 6 ] anionic centers for non-dissociative dinitrogen reduction, where hydridic H transports electron and proton between the centers, and the Li(Ba) cations for stabilizing N x H y (x: 0 to 2, y: 0 to 3) intermediates. The dynamic and synergistic involvement of all the components of the ternary complex hydrides facilitates a novel reaction mechanism with a narrow energy span and perfectly balanced kinetic barriers for the multi-step process, leading to ammonia production from N 2 +H 2 with superior kinetics under mild conditions.
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